Question 1

Acute Lymphoblastic Leukemia - very common in ____! - ___ is the second most common leukemia type in children (__ and ___ are rare in children) - peak age for ALL is __ to ___ - most common initial symptoms of ALL are attributable to ____ (low blood counts) and infiltration of ____ cells into organs - neoplastic accumulation of ___ (\>__%) in the BM - positive nuclear staining for ____ - increased blasts __ ___ normal hematopoiesis, resulting in acute presentation with anemia, thrombocytopenia, or neutropenia. - associated with __ __ and ___ mutation - marrow is ___cellular Treatment: 6MP Two Subtypes: 1. B. ALL - most common type of ALL in children (peak incidence 4 yo) Presentation: ___ --\> due to marrow expansion - ____ - due to decreased neutrophils Lymphadenopathy, splenomegaly, hepatomegaly --\> megaly's due to _____ being produced. - H/A and vomiting --\> due to ____ spread of lymphoblast. - Bone marrow ____ --\> due to lymphoblasts overtaking BM leading to anemia, thrombocytopenia, and neutropenia Markers: - (____+) that express ___, ___, and ___ (which one is also expressed in burkitt's and follicular lymphoma?) Genetics: - B A.L.L - many different translocations reported, but three are more important: 1. ____ t(__:___) translocation - ___:___ - 20-30% of A.L.L cause in ____! - 2-3% of A.L.L. cause in children ____ translocation is associated with poor prognosis. ____ creates fusion product of 2 genes. This is commonly seen in ___ and is a ____ prognosis. 2. t(12:21) translocation - creates fusion product of 2 genes: ___-____ --\> seen mostly in ____ - TEL-AML-1 impairs ____ of blasts and leads to acute leukemia. B. A.L.L. Risk Factors: - significantly higher risk in __ __ patients. - ___ ____ children - risk for ALL is 10-20X greater. 1 - 3% of all ALL cases have __ ___. Prognosis: ___:____ good prognosis (commonly seen in children) ___:____ worse prognosis (commonly seen in adults) ___ ___ ____ - most power predictor of prognosis - early response to therapy is the single most powerful prognostic predictor - B.ALL excellent response to chemo, but requires prophylaxis to __ and ___ (sanctuary sites) T.ALL T. ALL - characterized by lymphoblasts (___+) that express CD___ to ___. NOT ___. Presentation: - usually presents in older aged kids (___ to __ yo) or teenagers (_____\>____) as: - ____ WBC (remember, ___ WBC only seen in leukemias, not lymphomas) - _____ ____ --\> this is due to the thymus, where T cells develop, which makes sense that it would be enlarged - lymphadenopathy - __ ___ effusion and ___syndrome --\> the thymus is an anterior structure, so all mediastinal masses that occur in T.ALL are usually anterior and also associated with pleural effusion. - ____ obstruction --\> b/c tumor can get so large, that it can compress other structures and can cause ____ syndrome (compresses blood flow through SVC). The patient may presents with difficulty____. - CNS disease Markers: You will see different markers here than in B. A.L.L. In T.ALL, You will see CD____'s and may also see CD 2, 3, 5, 8, and 4. You will NOT see CD___ (CD___ ONLY FOUND ON PRE-B'S!) Note: it is called acute lymphoblastic LYMPHOMA because the malignant cells for a mass CD10 Expressers Burk's Balls Fall Treatment: 1. __ ____1 month) 2. ____(6-9 months) 3. _____ (2-3 years) 4. ____treatment (all throughout all above phases)

Accepted Answer

Acute Lymphoblastic Leukemia - very common in children! - AML is the second most common leukemia type in children (CLL and CML are rare in children) - peak age for ALL is 2-5 - most common initial symptoms of ALL are attributable to cytopenia (low blood counts) and infiltration of lymphoblasts cells into organs - neoplastic accumulation of lymphoblasts (\>20%) in the BM - positive nuclear staining for Tdt - increased blasts disrupt normal hematopoiesis, resulting in acute presentation with anemia, thrombocytopenia, or neutropenia. - associated with Down syndrome and IKZF1 mutation - marrow is hypercellular Treatment: 6MP Two Subtypes: 1. B. ALL - most common type of ALL in children (peak incidence 4 yo) Presentation: bone pain --\> due to marrow expansion - fever- due to decreased neutrophils Lymphadenopathy, splenomegaly, hepatomegaly --\> megaly's due to lymphoblasts being produced. - H/A and vomiting --\> due to meningeal spread of lymphoblast. - Bone marrow depression --\> due to lymphoblasts overtaking BM leading to anemia, thrombocytopenia, and neutropenia Markers: - (Tdt+) that express CD19, and CD10 (note: Burkitt's lymphoma and follicular lymphoma also expresses CD10) Genetics: - B A.L.L - many different translocations reported, but three are more important: 1. Philly t(9:22) translocation - 9:22 - 20-30% of A.L.L cause in adults! - 2-3% of A.L.L. cause in children 9:22 translocation is associated with poor prognosis. 9:22 creates fusion product of 2 genes. This is commonly seen in adults and is a poor prognosis. 2. t(12:21) translocation - creates fusion product of 2 genes: TEL-AML--\> seen mostly in children - TEL-AML-1 impairs maturation of blasts and leads to acute leukemia. B. A.L.L. Risk Factors: - significantly higher risk in down syndrome patients. - DS children - risk for ALL is 10-20X greater. 1 - 3% of all ALL cases have DS. Prognosis: 12:21 good prognosis (commonly seen in children) 9:22 worse prognosis (commonly seen in adults) MRD (minimal residual disease) - most powerful predictor of prognosis - early response to therapy is the single most powerful prognostic predictor - B.ALL excellent response to chemo, but requires prophylaxis to CNS and Scrotum (sanctuary sites) T.ALL T. ALL - characterized by lymphoblasts (TdT+) that express CD2 to 8. NOT CD10 Presentation: - usually presents in older aged kids (5 to 12yo) or teenagers (M\>F) as: - HIGH WBC (remember, HIGH WBC only seen in leukemias, not lymphomas) - MEDIASTINAL MASS --\> this is due to the thymus, where T cells develop, which makes sense that it would be enlarged - lymphadenopathy - ANTERIOR PLEURAL effusion and SVC syndrome --\> the thymus is an anterior structure, so all mediastinal masses that occur in T.ALL are usually anterior and also associated with pleural effusion. - TRACHEAL obstruction --\> b/c tumor can get so large, that it can compress other structures and can cause SVC syndrome (compresses blood flow through SVC). The patient may presents with difficulty BREATHING - CNS disease Markers: You will see different markers here than in B. A.L.L. In T.ALL, You will see CD7's and may also see CD 2, 3, 5, 8, and 4. You will NOT see CD10 (CD10 ONLY FOUND ON PRE-B'S!) Note: it is called acute lymphoblastic LYMPHOMA because the malignant cells for a mass Treatment: 1. REMISSION INDUCTION 1 month) 2. CONSOLIDTON (6-9 months) 3. MAINTENANCE (2-3 years) 4. CNS treatment (all throughout all above phases

Question 2

CML - neoplastic proliferation of mature ____ cells, especially _____ and their precursors (___ are characteristically increased) - ____ total WBC - differential reveals elevated neutrophils, bands, myelocytes, metamyelocytes, eosinophils, basophils and PLATELETS - will not see an accumulation of ____ in CML like you would see in AMLs. Genetics: - MUST HAVE ___:___ ___TRANSLOCATION with a breakpoint at ____ which generates __-___ fusion protein which increases __ __ activity. - when___:___ is always present, the tyrosine kinase is always on --\> this provides a constant signal that cause the cell to__. Cr. __ breakpoints: - p___ (___ kDa protein) = seen in ALL Presentation of CML: 3 Phases: 1. Chronic phase - Myeloid stem cell growing more than normal, but still \<___% blast in marrow. Chronic phase Lab Findings: - increased ____ (WBC = 100,000). - increase neutrophils, basophils and eosinophils. Note: Remember neutrophil development? Myeloblast --\> promyelocytes --\> myelocytes --\> bands. You can expect all of these to be ____ too. - few blasts \<___% Chronic Phase Presentation: - mild anemia, normal or increased platelets. - can be asymptomatic (increased WBCs on testing) - fatigue, malaise, wt. loss, splenomegaly - \<____% BLASTS IN MARROW --\> normal . .after a few years, chronic phase moves to ACCELERATED PHASE: 2. Accelerated Phase - treatment failure (rising WBCs), despite therapy. - ___-___% BLASTS IN THE MARROW ...accelerated phase will move to ACUTE PHASE 3. Acute phase (transformation) - ____ CRISIS --\> looks like AML (\>____% blasts in periphery or marrow), however, in order to diagnose with CML must have __;___ translocation! - usually, blasts are ____, so blast crisis is another version of ___. - Can turn into ___ or ___ transformations: - Can turn into ___ (2/3) or ____ (1/3), since there is a mutation is in a pluripotent stem cell Differential Diagnosis: CML or ____ Rxn? It is very important to distinguish CML from __ __ reaction (Leukomoid reaction), which is a normal response to infection. When you suspect CML, you must rule out the possibility that there is an occult infection going on. CML must be distinguished from a leukomoid reaction: - cml granulocytes are LAP ____ - cml is associated with increased ____(UNIQUE!!) - cml granulocytes exhibit t(___) LAP: Leukocyte alkaline phosphatase test - an enzyme found in normal ____ LAP - absent in neutrophils of __ - enzyme levels assessed with LAP score: If: ___ LAP --\> CML If: ____ LAP --\> leukomoid reaction Genetics: 9:22 - BCR-ABL fusion with increased tyrosine kinase activity which leads to long life. This fusion chromosome results in synthesis of tyrosine kinase protein that leads to long cell life --\> allows WBCs to evade apoptosis and live a long life. LAP has been largely replaced by testing for Philadelphia chromosome. Presentation: ___ IS COMMON! - enlarging ___ suggests accereleated phase of disease. - transformation to acute leukemia usually follows shortly thereafter Treatment: Because CML involves Ph Cr and over expression of __ ___ enzyme, a # of drugs have been developed to target this problem. 1. _____ (Gleevec) --\> first line tyrosine kinase inhibitor 2. Dasatinib 3. Nilotinib - these are used for treatment in CML (____ phase) - long term control of disease (not curative) - bone marrow transplant often used after failure Other notes: - Gleevec (Imatinib) resistance is developing. - During accelerated phase, use higher doses of ___. Imatinib binds to ___ on GISTs (GI stromal tumors) Imatinib binds to ___-alpha, which is seen in ___ ___

Accepted Answer

CML - neoplastic proliferation of mature myeloid cells, especially granulocytes and their precursors (BASOPHILS are characteristically increased) - INCREASED total WBC - differential reveals elevated neutrophils, bands, myelocytes, metamyelocytes, eosinophils, basophils and PLATELETS - will not see an accumulation of MYELOBLASTS in CML like you would see in AMLs. Genetics: - MUST HAVE 9:22 PHILLY TRANSLOCATION with a breakpoint at 210 which generates BCR-ABL fusion protein which increases TYROSINE KINASE activity. - when 9;22 is always present, the tyrosine kinase is always on --\> this provides a constant signal that cause the cell to GROW. Cr. 22 breakpoints: - p190 (190 kDa protein) = seen in ALL Presentation of CML: 3 Phases: 1. Chronic phase - Myeloid stem cell growing more than normal, but still \<5% blast in marrow. Chronic phase Lab Findings: - increased LEUKOCYTOSIS (WBC = 100,000). - increase neutrophils, basophils and eosinophils. Note: Remember neutrophil development? Myeloblast --\> promyelocytes --\> myelocytes --\> bands. You can expect all of these to be PRESENT too. - few blasts \<5% Chronic Phase Presentation: - mild anemia, normal or increased platelets. - can be asymptomatic (increased WBCs on testing) - fatigue, malaise, wt. loss, splenomegaly - \<5% BLASTS IN MARROW --\> normal . .after a few years, chronic phase moves to ACCELERATED PHASE: 2. Accelerated Phase - treatment failure (rising WBCs), despite therapy. - 6-19% BLASTS IN THE MARROW ...accelerated phase will move to ACUTE PHASE 3. Acute phase (transformation) - BLAST CRISIS --\> looks like AML (\>20% blasts in periphery or marrow), however, in order to diagnose with CML must have 9;22 translocation! - usually, blasts are MYELOBLAST, so blast crisis is another version of AML - Can turn into AML or ALL transformations: - Can turn into AML 2/3) or ALL (1/3), since there is a mutation is in a pluripotent stem cell Differential Diagnosis: CML or LEUKOMOID Rxn? It is very important to distinguish CML from LEFT SHIFT reaction (Leukomoid reaction), which is a normal response to infection. When you suspect CML, you must rule out the possibility that there is an occult infection going on. CML must be distinguished from a leukomoid reaction: - cml granulocytes are LAP NEGATIVE - cml is associated with increased BASOPHILS (UNIQUE!!) - cml granulocytes exhibit t(9;22) LAP: Leukocyte alkaline phosphatase test - an enzyme found in normal NEUTROPHILS LAP - absent in neutrophils in CML - enzyme levels assessed with LAP score: If: LOW LAP --\> CML If: HIGH LAP --\> leukomoid reaction Genetics: 9:22 - BCR-ABL fusion with increased tyrosine kinase activity which leads to long life. This fusion chromosome results in synthesis of tyrosine kinase protein that leads to long cell life --\> allows WBCs to evade apoptosis and live a long life. LAP has been largely replaced by testing for Philadelphia chromosome. Presentation: SPLENOMEGALY IS COMMON! - enlarging SPLEEN suggests accereleated phase of disease. - transformation to acute leukemia usually follows shortly thereafter Treatment: Because CML involves Ph Cr and over expression of TYROSINE KINASE enzyme, a # of drugs have been developed to target this problem. 1. IMATINIB (Gleevec) --\> first line tyrosine kinase inhibitor 2. Dasatinib 3. Nilotinib - these are used for treatment in CML (CHRONIC phase) - long term control of disease (not curative) - bone marrow transplant often used after failure Other notes: - Gleevec (Imatinib) resistance is developing. - During accelerated phase, use higher doses of TKI. Imatinib binds to C-KIT on GISTs (GI stromal tumors) Imatinib binds to PDGFR-alpha, which is seen in HYPEREOSINOPHILIC SYNDROME

Question 3

Chronic Lymphocytic Leukemia - CLL - neoplastic proliferation of ____ that co express CD___ (unique and also seen in mantle cell and SLL) CD___, CD___, CD___ (+/-) CD___ - most common leukemia overall (C for Common) - but uncommon in ____! 4 STAGES OF CLL low = 0 - ____ only intermediate I - lymphocytosis, ____ intermeidiate II - lymphocytosis, ____ High - III - lymphocytosis, with Hb \<____ due to progression of CLL in marrow High IV - lymphocytosis, ___ \<__ K due to progression of CLL in marrow Presentation: - lymphadenopathy (lymphadenopathy not seen in hairy cell leukemia) --\> b/c involvement of lymph nodes - splenomegaly - hepatomegaly Note: when patients are diagnosed, many of them are just observed and go without treatment Markers: CD_, CD__, CD___, CD___a and CD__ are co-expressed. Unique b/c CD__ = a typical B cell receptor and CD__, typical T cell receptor are expressed together . Diagnosis: - lots of ___s! SLL is similar to CLL. They have the same malignant cells, but the disorders are differentiated by their WBC count. ____ - lymphocyte \< 5000 ___ - lymphocyte \> 5000 Lab Findings: __ cells! - Peripheral lymphocytes are fragile and are disrupted during preparation of blood smear . Epidemiology: - median age of diagnosis is 60 - Pt is often ____. - CLL often noticed when a pt gets a routine CBC - physician will notice increased lymphocytes. - ___-___ % of patients will have___ symptoms (fever, sweats). Complications: __ __ 1. ____ --\> B cells produce antibodies, so many patients with CLL will develop hypogammaglobulinemia with decreased levels of IgG, IgA, and IgM --\> increased susceptibility to bacterial infections! 2. ____ --\> autoimmune antibodies. These aren't produced by malignant cells, but from ____ cells. This causes autoimmune hemolytic anemia! 3. ___ ____ --\> Can transform to diffuse B cell lymphoma (which other lymphoma can do this?) -- marked clinically by enlarged spleen or lymph node --\> CLL may also transform tissue into large B cell lymphomas How can we tell if a CLL patient's thrombocytopenia is from ITP or stage IV disease? - do a bone marrow biopsy - In stage IV CLL, you will see ___ platelet count AND absent ____ in BM (b/c CLL has taken over) - In CLL (not stage IV) and ITP, you will see ___ platelet counts, but you will see ____ in the BM. Treatment for CLL and ITP- ___ Treatment for stage IV CLL - ___ __ and BM transplant. Classic presentation: - patient with h/o CLL and suddenly sees rapid growth of ___ ___ lymphoma. Treatment: bone marrow transplant but only if they have symptoms (stage 3 or 4 ... Hb \<11 and Plts \< 100K)

Accepted Answer

Chronic Lymphocytic Leukemia - CLL - neoplastic proliferation of naive B cells that co express CD5 (unique) CD19, CD79a, CD23 (+/-) CD20 - most common leukemia overall (C for Common) - but uncommon in children! 4 STAGES OF CLL low = 0 - lymphocytosis only intermediate I - lymphocytosis, lymphadenopathy intermeidiate II - lymphocytosis, splenomegaly High - III - lymphocytosis, with Hb \<11.0 due to progression of CLL in marrow High IV - lymphocytosis, platelets \<100 K due to progression of CLL in marrow Presentation: - lymphadenopathy (lymphadenopathy not seen in hairy cell leukemia) --\> b/c involvement of lymph nodes - splenomegaly - hepatomegaly Note: when patients are diagnosed, many of them are just observed and go without treatment Markers: CD5, CD19, CD20, CD79a and CD23 are co-expressed. Unique b/c CD20 = a typical B cell receptor and CD5, typical T cell receptor are expressed together . Diagnosis: - lots of WBCss! SLL is similar to CLL. They have the same malignant cells, but the disorders are differentiated by their WBC count. CLL - lymphocyte \< 5000 SLL - lymphocyte \> 5000 Lab Findings: smuge cells! - Peripheral lymphocytes are fragile and are disrupted during preparation of blood smear . Epidemiology: - median age of diagnosis is 60 - Pt is often asymptomatic - CLL often noticed when a pt gets a routine CBC - physician will notice increased lymphocytes. - 5-10 % of patients will have B symptoms (fever, sweats). Complications: Immune dysregulation 1. Hypogammaglobulinemia --\> B cells produce antibodies, so many patients with CLL will develop hypogammaglobulinemia with decreased levels of IgG, IgA, and IgM --\> increased susceptibility to bacterial infections! 2. AIHA --\> autoimmune antibodies. These aren't produced by malignant cells, but from self cells. This causes autoimmune hemolytic anemia! 3. Richter transformation --\> Can transform to diffuse B cell lymphoma (like follicular lymphoma)-- marked clinically by enlarged spleen or lymph node --\> CLL may also transform tissue into large B cell lymphomas How can we tell if a CLL patient's thrombocytopenia is from ITP or stage IV disease? - do a bone marrow biopsy - In stage IV CLL, you will see low platelet count AND absent megakaryocytes in BM (b/c CLL has taken over) - In CLL (not stage IV) and ITP, you will see low platelet counts, but you will see megakaryocytes in the BM. Treatment for CLL and ITP- predisone Treatment for stage IV CLL - cytotoxic chemo and BM transplant. Classic presentation: - patient with h/o CLL and suddenly sees rapid growth of B cell lymphoma. Treatment: bone marrow transplant but only if they have symptoms (stage 3 or 4 ... Hb \<11 and Plts \< 100K)

Question 4

Follicular Lymphoma - most common low grade non-hodgkin lymphoma - ____% of all new NHL diagnosis - neoplastic proliferation of __ ___ cells (CD20) that form ___-like nodules - Usually, expresses CD___ and CD___, and ___-__ - Most cells express surface immunoglobulins - _____ lymphadenopathy - follicular lymphoma cells consists of ____, the small ____cells, and centro____, larger cells that divide more. - the larger the number of___, the more aggressive the follicular lymphoma Epidemiology: - presents in ___ Markers: name 3 ___. ___. ___, ___ Presentation: - _____ lymphadenopathy - ____ course: __ and ____ for years - not all patients require___, however, ___ to cure Genetics: - t(___;____) - 85% of patients have a translocation of heavy chain Ig (___) to ____ (Cr. 18) - Causes ____ over expression! - __ over expression blocks___ (____ is an antagonist of __) Cr. 14: ___ locus Cr. 18:____ locus Differential Diagnosis: You must be able to distinguish FL from ___ ___ ____!!! The presence of _____ set reactive LAD apart from follicular lymphoma!! LAD and FL both have high ____ growth! But: - LAD has high follicular growth due to __ __. There is also varying __ and ___ in these B cells. There is____ of many B cells as a result and lots of death. This causes lots of cellular ___ which is cleaned up by ____ --\> the presence of ____ set reactive LAD apart from follicular lymphoma. ____ ARE seen in LAD, but not in follicular lymphoma. - Germinal center B cells usually lack ____. - Most B cells undergo ____ unless selected by __ ___. Prognosis: Not___, but is ____. ____ is a feared consequence of follicular lymphoma. Histology transformation occurs ___ to ___% of cases. When this happens, prognosis is ___! Treatment: - reserved for people who are _____ - if symptomatic, use low dose chemo, or ____ (anti CD____) Complications: - progression to diffuse large B cell lymphoma - presents as an enlarging ___ _____ (SAME AS IN HCL)

Accepted Answer

Follicular Lymphoma - most common low grade non-hodgkin lymphoma - 22% of all new NHL diagnosis - neoplastic proliferation of SMALL B CELLS cells (CD20) that form FOLLICULE-like nodules - Usually, expresses CD10, CD19 and CD20, and BCL-2 - Most cells express surface immunoglobulins - PAINLESS lymphadenopathy - follicular lymphoma cells consists of CENTROCYTES, the small CLEAVED cells, and centroBLASTS, larger cells that divide more. - the larger the number of CENTROBLASTS, the more aggressive the follicular lymphoma Epidemiology: - presents IN ELDERLY Markers: CD19, CD20, BCL2, CD10 Presentation: - PAINLESS lymphadenopathy - INDOLENT course: WAXES and WANES for years - not all patients require TREATMENT, however, DIFFICULT to cure Genetics: - t(14;18) - 85% of patients have a translocation of heavy chain Ig (Cr. 14) to BCL (Cr. 18) - Causes BCL2 over expression! - BCL2 over expression blocks APOPTOSIS (BCL2 is an antagonist of CELL DEATH) Cr. 14: IGH locus Cr. 18: BCL locus Differential Diagnosis: You must be able to distinguish FL from REACTIVE LYMPHADENOPATHY!!! The presence of MACROPHAGES set reactive LAD apart from follicular lymphoma!! LAD and FL both have high FOLLICULAR growth! But: - LAD has high follicular growth due to SOMATIC HYPERMUTATION. There is also varying SIZES and SHAPES in these B cells. There is APOPTOSIS of many B cells as a result and lots of death. This causes lots of cellular DEBRIS which is cleaned up by MACROPHAGES--\> the presence of MACROPHAGES set reactive LAD apart from follicular lymphoma. MACROPHAGES ARE seen in LAD, but not in follicular lymphoma. - Germinal center B cells usually lack BCL2. - Most B cells undergo APOPTOSIS unless selected by SOMATIC HYPERMUTATION. Prognosis: Not CURABLE, but is TREATABLE DLBCL is a feared consequence of follicular lymphoma. Histology transformation occurs 10 to 70% of cases. When this happens, prognosis is POOR! Treatment: - reserved for people who are SYMPTOMATIC - if symptomatic, use low dose chemo, or RITUXIMAB (anti CD20) Complications: - progression to diffuse large B cell lymphoma - presents as an enlarging PAINLESS LYMPHADENOPATHY

Question 5

Diffuse Large B Cell (DLBCL) - Most ___ aggressive NH lymphoma - Neoplastic ____ ___ __ (CD__) - Clinically AGGRESSIVE - occurs in ___. An ____ DEFINING MALIGNANCY - arises sporadically from transformation of ____ lymphoma OR ___ ___ ____ Epidemiology: - affects usually _____ but affects ___% of children Genetics: - 30% of patients have a ___;___ translocation - Alternations in ___ and ____ Markers: - expression of CD___ and CD___ Presentation: - presents late in adulthood as an enlarging LN or ___ ___ mass Treatment: Name 5 drugs

Accepted Answer

Diffuse Large B Cell (DLBCL) - Most COMMON aggressive NH lymphoma - Neoplastic LARGE B CELL LYMPHOMA (CD20) - Clinically AGGRESSIVE - occurs in HIV. An AIDS DEFINING MALIGNANCY - arises sporadically from transformation of FOLLICULAR lymphoma or chronic lymphocytic leukemia. Epidemiology: - affects usually OLDER ADULTS but affects 20% of children Genetics: - 30% of patients have a 14;18 translocation - Alternations in BCL2 and BCL6 Markers: - expression of CD19 and CD20 Presentation: - presents late in adulthood as an enlarging LN or EXTRA NODALmass Treatment: R-CHOP Name 5 drugs RITUXIMAB CYCLOPHOSPHAMIDE HYDROXY-DOXORUBICIN ONCOVIN- VINCRISTINE PREDNISONE

Question 6

Burkitt Lymphoma - Neoplastic of ____ (CD___ and CD__) - associated with ____ - one of the fastest growing tumors that exist - doubling time is __ to __ hrs - Usually express CD___, CD____ and CD__ - VERY ____ --\> rapidly proliferative Epidemiology: - affects adolescents of young adults - ___ form - involves jaw - Sporadic form - involves ___ Genetics: - t(__;___) translocation - but can also be __;___ translocation or ___;___ translocation. _____ nuclear regulator) gene is translocated. lots of ___ --\> causes lots of growth! - ___ gene found on Cr. __. What is ____? ____ is a growth promoter. Often, it is translocated to Cr. ___ (where ___ B cell heavy chain gene is located). This translocation leads to over expression of ___ gene on B cells and causes ____. Diagnosis - need tissue sample (because it is NOT in the blood) - ____% Ki-67 staining (Ki-67 shows us how many cells are ___) Lab Findings: __-___ appearance --\> numerous rapidly dividing Burkitt Lymphoma cells create lots of ___. This debris is cleared by ____ which create a clearing space. This gives Burkitts Lymphoma a __ ___ appearance. Three forms: 1. Endemic - African and New Guinea - found in Africa and New Guinea - __-___% of childhood cancer in some regions b/c such a large prevalence of EBV. - affects children __-__ years old (typically young ___) - - Commonly presents as a mass in ____ (classic presentation) - tumor cells originate from a single ___-infected B cell so ___ is almost always found. 2. Sporadic - usually what we see in the US - involves the abdomen, ovaries, kidneys, momentum, extra nodal sites, walldeyers rings. - also occurs in ___ - This form presents as an ___ mass in ___ OR ____ 3. Immunodeficiency type - primarily occurs in patients affected with ___, also seen in ___ recipients, ____ immunodeficiency states - accounts for__-___% of all NHL in __ pts Other AIDS defining malignancies: - ___ sarcoma - Systemic __ - ___ cancer

Accepted Answer

Burkitt Lymphoma - Neoplastic of intermediate sized B cells (CD20 and CD10) - associated with EBV - one of the fastest growing tumors that exist - doubling time is 24 to 48 hrs - Usually express CD10, CD19and CD20 - VERY ____ --\> rapidly proliferative Epidemiology: - affects adolescents of young adults - ENDEMIC form - involves jaw - Sporadic form - involves ABDOMEN Genetics: - t(8;14) translocation - but can also be 8;22 translocation or 8;2 translocation. c-myc nuclear regulator) gene is translocated. lots of cmyc --\> causes lots of growth! -cmyb gene found on Cr. 8. What is cmyc? cmycis a growth promoter. Often, it is translocated to Cr. 14 (where Ig B cell heavy chain gene is located). This translocation leads to over expression of cmyc gene on B cells and causes overgrowth. Diagnosis - need tissue sample (because it is NOT in the blood) - 100% Ki-67 staining (Ki-67 shows us how many cells are dividing) Lab Findings: starry-sky appearance --\> numerous rapidly dividing Burkitt Lymphoma cells create lots of debris. This debris is cleared by macrophages which create a clearing space. This gives Burkitts Lymphoma a starry sky appearance. Three forms: 1. Endemic - African and New Guinea - found in Africa and New Guinea - 20-30% of childhood cancer in some regions b/c such a large prevalence of EBV. - affects children 4-7 years old (typically young boys) - - Commonly presents as a mass in mandible (classic presentation) - tumor cells originate from a single EBV -infected B cell so EBV is almost always found. 2. Sporadic - usually what we see in the US - involves the abdomen, ovaries, kidneys, momentum, extra nodal sites, walldeyers rings. - also occurs in CHILDREN - This form presents as an ABDOMINAL mass in ILEOCECUM OR PERITONEUM 3. Immunodeficiency type - primarily occurs in patients affected with HIV, also seen in ALLOGRAFT recipients, CONGENITAL immunodeficiency states - accounts for 30-40% of all NHL in AIDS pts Other AIDS defining malignancies: - KAPOSI sarcoma - Systemic NHL - CERVICAL cancer

Question 7

Polycythemia Vera - neoplastic proliferation of mature myeloid cells, especially ___ ___ cells. - granulocytes and platelets are also increased Genetics: - associated with ___ mutation Hgb: __ (normal 15) Hct: __ (normal 45) Presentation: - symptoms mostly due to ___ blood - blurry ___ and ___ ache - ___ face (facial ___) due to congestion. Also, increased RBC leads to increase in blood ____, which causes ___ and ___ - increased risk for venous thrombosis from too many ____ and ____ blood (e.g. hepatic vein, portal vein, dural sinuses). classically, ___-___ syndrome (blood clot in ___ vein) --\> when you get a thrombosis in the hepatic vein which gives infarct in the liver - ___-____ ____ - an unbearable itching after bathing because lots of ___ cells - increased plasma___ . Note: many patients ____ (usually discovered after routine CBC) Differential Diagnosis: PV MUST BE DISTINGUSHED FROM __ ___! Why? --\> if we have increased RBC, that could actually be due to another condition. For example, lets say that someone has lung disease, then their saturation O2 would be ___, and EPO would be ____. - We could also get reactive PV from topic EPO production from renal cell carcinoma. - In RCC, EPO is ____ and SaO2 is ___. BUT...in PV, SaO2 is ____ and EPO is ____ due to ___ ____ b/c so many RBCs\ So, when diagnosing PV, we must exclude: - ___ from lung disease) - __ __ ___ (from too much EPO being produced by cancer) Treatment: - ____ (take away RBCs) - second line - ___ - inhibits replication of RBC Note: without treatment, death usually occurs within a year. Complications: 1. Spent phase (~15% of patients) - BM gets burned out and there is BM ___. This leads to ___ 2. Leukemia - usually progresses to __ -- rarely to ___ 3. ____ - excess DNA turnover from increased RBC production. This can inrease ____ metabolism using to increased uric acid --\> ____. Note that this also happens in ___.

Accepted Answer

Polycythemia Vera - neoplastic proliferation of mature myeloid cells, especially RB cells. - granulocytes and platelets are also increased Genetics: - associated with JAK2 mutation Hgb: 20 (normal 15) Hct: 60 (normal 45) Presentation: - symptoms mostly due to VISCOUS blood - blurry VISION and HEADACHE - FLUSHED face (facial PLETHORA due to congestion. Also, increased RBC leads to increase in blood VOLUME, which causes HYPERTENSION and THROMNBOSIS - increased risk for venous thrombosis from too many PLATELETS and VISCOUS blood (e.g. hepatic vein, portal vein, dural sinuses). classically, BUDD-CHIARI syndrome (blood clot in PORTAL vein) --\> when you get a thrombosis in the hepatic vein which gives infarct in the liver - AQUA-GENIS PRURITIS - an unbearable itching after bathing because lots of MAST cells - increased plasma VOLUME. Note: many patients ASYMPTOMATIC (usually discovered after routine CBC) Differential Diagnosis: PV MUST BE DISTINGUSHED FROM REACTIVE POLYCYTHEMIA VERA! Why? --\> if we have increased RBC, that could actually be due to another condition. For example, lets say that someone has lung disease, then their saturation O2 would be LOW , and EPO would be NORMAL. - We could also get reactive PV from topic EPO production from renal cell carcinoma. - In RCC, EPO is HIGH and SaO2 is NORMAL BUT...in PV, SaO2 is NORMAL and EPO is DECREASED due to NEGATIVE FEEDBACK b/c so many RBCs\ So, when diagnosing PV, we must exclude: - HYPOXIA from lung disease) - RENAL CELL CARCINOMA (from too much EPO being produced by cancer) Treatment: - PHLEBOTOMY (take away RBCs) - second line - HYDROXYUREA - inhibits replication of RBC Note: without treatment, death usually occurs within a year. Complications: 1. Spent phase (~15% of patients) - BM gets burned out and there is BM FAILURE. This leads to MYELOFIBROSIS 2. Leukemia - usually progresses to AML -- rarely to CML 3. GOUT - excess DNA turnover from increased RBC production. This can inrease PURINE metabolism using to increased uric acid --\> GOUT. Note that this also happens in CML.

Question 8

Essential Thrombocythemia - malignant proliferation of ____cells, especially _____ Genetics: - associated with ____ mutation - predominantly affects ____/____ Presentation: - increased risk of ___ and/or ___ --\> although there is an ____ in platelet count, they are not functioning properly, so you can still get bleeding or you can get thrombosis. - rarely progresses to marrow ____ or acute leukemia - no significant risk for ___ OR ____ - abnormal ___ function Differential Diagnosis: - must exclude other _____ disorders. In ___ and ___, you can ALSO see higher platelet count so you must rule CML and PV out first. In addition, you must exclude out ___ __. This causes high platelets because of another condition such as in: - infections - metastatic cancer - acute bleeding, hemolysis Key blood tests: - measure RBC and test for __ __ ___. So, if C-reactive protein, fibrinogen, ESR or ferritin is high, then there could be high platelets due to an occult _____ reaction. Prognosis: - Most patients have no disease related complications. PV complications are unusual Treatment: ___, ____

Accepted Answer

Essential Thrombocythemia - malignant proliferation of MATURE MYELOID cells, especially MEGAKARYOCYTES Genetics: - associated with JAK2 mutation - predominantly affects MEGAKARYOCYTES/PLATELETS Presentation: - increased risk of BLEEDING and/or THROMBOSIS--\> although there is an INCREASE in platelet count, they are not functioning properly, so you can still get bleeding or you can get thrombosis. - rarely progresses to marrow FIBROSIS or acute leukemia - no significant risk for HYPERURECEMIA OR GOUT - abnormal PLATELET function Differential Diagnosis: - must exclude other MYELOPROLIFERATIVE disorders. In CML AND PV, you can ALSO see higher platelet count so you must rule CML and PV out first. In addition, you must exclude out REACTIVE THROMBOCYTHEMIA. This causes high platelets because of another condition such as in: - infections - metastatic cancer - acute bleeding, hemolysis Key blood tests: - measure RBC and test for ACUTE PHASE REACTANTS. So, if C-reactive protein, fibrinogen, ESR or ferritin is high, then there could be high platelets due to an occult INFLAMMATION reaction. Prognosis: - Most patients have no disease related complications. PV complications are unusual Treatment: ASPIRIN, HYDROXYUREA

Question 9

MYELOFIBROSIS - neoplastic proliferation of mature myeloid cells, especially _____ Genetics: - associated with __ MUTATION (50% of time) - excess ____ form fibroblast leads to marrow ___ - ___ overtakes BM causing ___ Growth Factors:____ AND ____ Pathophysiology of primary myelofibrosis - marrow finding --\> __ ___ hematopoiesis. - when bone marrow fails, organs like the spleen, liver, and lymph nodes to undergo __ ___hematopoiesis - can be seen in CNS, lungs, bladder and even skin! Epidemiology - affects ___ Presentation - MASSIVE __ - once the bone marrow is ____, hematopoiesis can no longer occur. As a result, stem cells go back to making cells in the ___ AND ___ (like it was in the fetus). But, because there is massive extra hematopoiesis, you will see an ___ spleen. - fatigue, wt loss and night sweets --\> due to increased ____ - __ ___ abdominal pain --\> due to ___! - early ___ (due to ___ ____) - may also see enlarged lymph nodes - infection, thrombosis, bleeding --\> b/c BM can't properly make red, white and platelet cells. - Hyperuricemia - ____ --\> due to high cell turnover --\> increased metabolism due to extra medullary hematopoiesis b/c BM is nonfunctioning Lab Findings: - _____ smear - inappropriate release of cells from marrow - you will see immature __ and ___ precursors in blood - ___ ___ CELLS (____) is a CLASSIC finding in myelofibrosis. This is because RBCs are ___ as they squeeze through the fibrosis marrow!! What is a leukoerythoblastic smear? - When cells are made in the bone marrow, the BM has ____ gates. These gates prevent cells that are immature from exiting in the blood. These gates are made up of reticulin. In the spleen, when extra medullary hematopoiesis occurs, we won't be able to prevent immature cells from leaving the spleen, so we get ____ cells (increased white, red, and immature cells in blood--we will end up seeing ____ blood cells). - increased risk of infection, thrombosis and bleeding --\> b/c BM can't properly make red, white and platelet cells. The vast majority of cell production has shifted over to the ___, however, the spleen is tiny compared to BM, so even though pt undergoes extrahematopoiesis, it is no where where they need to be. Treamtment:__ __ __

Accepted Answer

MYELOFIBROSIS - neoplastic proliferation of mature myeloid cells, especially MEGAKARYOCYTES Genetics: - associated with JAK2 MUTATION (50% of time) - excess COLLAGEN form fibroblast leads to marrow FIBROSIS - COLLAGEN overtakes BM causing FIBROSIS Growth Factors:PDGF AND TGF-B Pathophysiology of primary myelofibrosis - marrow finding --\> EXTRA MEDULLARY hematopoiesis. - when bone marrow fails, organs like the spleen, liver, and lymph nodes to undergo EXTRAMEDULLARY hematopoiesis - can be seen in CNS, lungs, bladder and even skin! Epidemiology - affects OLDER PEOPLE Presentation - MASSIVE SPLENOMEGALY - once the bone marrow is FIBROSED, hematopoiesis can no longer occur. As a result, stem cells go back to making cells in the SPLEEN AND LIVER (like it was in the fetus). But, because there is massive extra hematopoiesis, you will see an ENLARGED spleen. - fatigue, wt loss and night sweets --\> due to increased METABOLISM - LEFT UPPER abdominal pain --\> due to SPLEEN! - early SATIETY(due to COMPRESSED STOMACH) - may also see enlarged lymph nodes - infection, thrombosis, bleeding --\> b/c BM can't properly make red, white and platelet cells. - Hyperuricemia - GOUT --\> due to high cell turnover --\> increased metabolism due to extra medullary hematopoiesis b/c BM is nonfunctioning Lab Findings: - LEUKOERYTHBLASTIC smear - inappropriate release of cells from marrow - you will see immature GRANULOCYTE and RBC precursors in blood - TEAR DROP CELLS (DACROCYTES) is a CLASSIC finding in myelofibrosis. This is because RBCs are DEFORMED as they squeeze through the fibrosis marrow!! What is a leukoerythoblastic smear? - When cells are made in the bone marrow, the BM has RETICULATED gates. These gates prevent cells that are immature from exiting in the blood. These gates are made up of reticulin. In the spleen, when extra medullary hematopoiesis occurs, we won't be able to prevent immature cells from leaving the spleen, so we get LEUKOERYTHOBLASTIC cells (increased white, red, and immature cells in blood--we will end up seeing NUCLEATED blood cells). - increased risk of infection, thrombosis and bleeding --\> b/c BM can't properly make red, white and platelet cells. The vast majority of cell production has shifted over to the SPLEEN, however, the spleen is tiny compared to BM, so even though pt undergoes extrahematopoiesis, it is no where where they need to be. Treamtment: STEM CELL REPLACEMENT

Question 10

Hodgkin Lymphoma

(40%) - neoplastic proliferation of REED STERNBERG CELLS, which are large B cells with multi lobed nuclei and prominent nucleoli “owl eyes”

classically, POSITIVE FOR CD15 AND CD30
HL spreads in a very PREDICTABLE manner.

Epidemiology: - HL has a BIMODAL distribution - peaks at 20 and 60.

Presentation: - Enlarged PAINLESS LYMPH node. this is similar to HCL.

PAINLESS is the key word! PAINFUL lymph nodes are seen in infections, and these “reactive” lymph nodes are tender to touch.

So, enlarged painless lymph nodes suggest malignancy such as lymphomas.

REED STERNBERG Cells - secrete CYTOKINES - CAUSING “B” symptoms
lymphadenopathy and systemic symptoms caused by REED STERNBERG CELL release of CYTOKINES (include symptoms like fever, chills, wt. loss, night sweats).
cytokines attract lymphocyte, plasma cells, Macs and eosinophils (makes up the BULK of the tumor) -

RSC these are large multi lobed cells. Two halves are often mirror images of each other and look like “owl’s eyes.”

RS cells are usually CD15 And CD30 positive!
attract reactive lymphocytes, plasma cells, macrophages and eosinophils - may lead to FIBROSIS

(Note: although RS cells are in Hodgkin Lymphoma, they can also be seen in other disorders)

The malignant cell in Hodgkin Lymphoma is the Reed Sternberg cell. The cell is actually a minority in the cells that make up the enlarged lymph node. (only about 1-5%). The bulk of the cells are reacting to the presence of the RS cell’s release of large cytokines. If you remember, RS cells release lots of cytokines too. This can help you to remember that B symptoms are more common in Hodgkin lymphoma than in nonhodgkin lymphoma.

In addition, HL may lead to hyper-CALCEMIA. Why?

b/c one of the reactive cell types are MACROPHAGES which have 1-ALPHA-HYDROXYLASE, and enzyme which converts 25-OH-VIT-D to 1,25-OH-VIT D

Risk Factors: - prior EBV infection (virus infects B cells)

immunosuppresants
autoimmune diseases (RA, SLE)

Treatment: chemotherapy and radiation therapy, BLEOMYCIN

4 types:

Nodular sclerosing - most common (70%)

Classical Presentation: - enlarging CERVICAL neck or MEDIASTINAL LN in a YOUNG adult (usually FEMALE)

Lab Findings: - LACUNAR VARIANT REEDSTERNBERG cells seen in clear LAKE-LIKE spaces

Fibrous tissue surrounds a portion of tumor, creating nodules (NS type get its name because of this)

Prognosis: - Slow growth –> indolent - GOOD long term survival for the patient

Mixed Cellularity - associated with abundance of EOSINOPHILS (called in by IL-5 which is produced by _REEDSTERNBERG cells) - will also see eosinophils, neutrophils, macrophages, plasma cells
Lymphocyte Rich: - GOOD prognosis
Lymphocyte poor ; - BAD PROgnosis

Accepted Answer

Hodgkin Lymphoma

(40%) - neoplastic proliferation of REED STERNBERG CELLS, which are large B cells with multi lobed nuclei and prominent nucleoli “owl eyes”

classically, POSITIVE FOR CD15 AND CD30
HL spreads in a very PREDICTABLE manner.

Epidemiology: - HL has a BIMODAL distribution - peaks at 20 and 60.

Presentation: - Enlarged PAINLESS LYMPH node. this is similar to HCL.

PAINLESS is the key word! PAINFUL lymph nodes are seen in infections, and these “reactive” lymph nodes are tender to touch.

So, enlarged painless lymph nodes suggest malignancy such as lymphomas.

REED STERNBERG Cells - secrete CYTOKINES - CAUSING “B” symptoms
lymphadenopathy and systemic symptoms caused by REED STERNBERG CELL release of CYTOKINES (include symptoms like fever, chills, wt. loss, night sweats).
cytokines attract lymphocyte, plasma cells, Macs and eosinophils (makes up the BULK of the tumor) -

RSC these are large multi lobed cells. Two halves are often mirror images of each other and look like “owl’s eyes.”

RS cells are usually CD15 And CD30 positive!
attract reactive lymphocytes, plasma cells, macrophages and eosinophils - may lead to FIBROSIS

(Note: although RS cells are in Hodgkin Lymphoma, they can also be seen in other disorders)

The malignant cell in Hodgkin Lymphoma is the Reed Sternberg cell. The cell is actually a minority in the cells that make up the enlarged lymph node. (only about 1-5%). The bulk of the cells are reacting to the presence of the RS cell’s release of large cytokines. If you remember, RS cells release lots of cytokines too. This can help you to remember that B symptoms are more common in Hodgkin lymphoma than in nonhodgkin lymphoma.

In addition, HL may lead to hyper-CALCEMIA. Why?

b/c one of the reactive cell types are MACROPHAGES which have 1-ALPHA-HYDROXYLASE, and enzyme which converts 25-OH-VIT-D to 1,25-OH-VIT D

Risk Factors: - prior EBV infection (virus infects B cells)

immunosuppresants
autoimmune diseases (RA, SLE)

Treatment: chemotherapy and radiation therapy, BLEOMYCIN

4 types:

Nodular sclerosing - most common (70%)

Classical Presentation: - enlarging CERVICAL neck or MEDIASTINAL LN in a YOUNG adult (usually FEMALE)

Lab Findings: - LACUNAR VARIANT REEDSTERNBERG cells seen in clear LAKE-LIKE spaces

Fibrous tissue surrounds a portion of tumor, creating nodules (NS type get its name because of this)

Prognosis: - Slow growth –> indolent - GOOD long term survival for the patient

Mixed Cellularity - associated with abundance of EOSINOPHILS (called in by IL-5 which is produced by _REEDSTERNBERG cells) - will also see eosinophils, neutrophils, macrophages, plasma cells
Lymphocyte Rich: - GOOD prognosis
Lymphocyte poor ; - BAD PROgnosis

Question 11

Marginal Zone Lymphoma - neoplastic proliferation of __ __ ___ (CD20) that expands that ___ zone - associated with chronic ___ (e.g. ___, ____, ____) - B-cell malignancy that is adjacent to the ___ cells (___ zone is next to mantle cells which are next to ___) - Most lymph nodes don't have a ____ zone. The zone is formed only when there is activation of the cells through the germinal center. So, when cells go to the germinal cells and get activated (b/c of chronic inflammation), that is when the marginal zone is produced. So, the MZL is classically seen in ___ inflammatory states such as in: - __ ___ in Sjogren's - ____gland in Hashimoto - ____ stomach infections --\> MALToma (MALToma's are a form of marginal zone lymphomas Epidemiology - affects____ Genetics: - t(___;____)

Accepted Answer

Marginal Zone Lymphoma - neoplastic proliferation of small B cellv(CD20) that expands that mantle zone - associated with chronic inflammation (e.g. Sjogrens, IBS, MALTomas) - B-cell malignancy that is adjacent to the mantle cells (marginal zone is next to mantle cells which are next to follicles) - Most lymph nodes don't have a marginal zone. The zone is formed only when there is activation of the cells through the germinal center. So, when cells go to the germinal cells and get activated (b/c of chronic inflammation), that is when the marginal zone is produced. So, the MZL is classically seen in chronic inflammatory states such as in: - salivary glands in Sjogren's - thyroid gland in Hashimoto - h pylori stomach infections --\> MALToma (MALToma's are a form of marginal zone lymphomas Epidemiology - affects adults Genetics: - t(11:18)

Question 12

Mantle Cell Lymphoma - VERY ___ - neoplastic __ __ cells (CD20) that expand the ___ zone (mantle cell is immediately adjacent to the follicle) - arises from follicle ___ or sometimes ___ cells. Epidemiology: - Affects adult ___ (males __ females) Median Overall Survival - __ to __ years (___ prognosis) Markers: CD___ and CD___ (and CD19) - like SLL and CLL! Genetics: - ___:___ translocations (__ to __%) - Do you remember what was on Cr. 14? ---\> ___ ___!! - What gets translocated there? ---\> ____! What does over expression of ___ do? --\> _____ the regulators which makes the cell cycle to go from ___ to ___ facilitating neoplastic proliferation.

Accepted Answer

Mantle Cell Lymphoma - VERY AGGRESSIVE - neoplastic SMALL B cells (CD20) that expand the MANTLE zone (mantle cell is immediately adjacent to the follicle) - arises from follicle MANTLE or sometimes GERMINAL cells. Epidemiology: - Affects adult MALES (males \>females) Median Overall Survival - 3 to 4 years (POOR prognosis) Markers: CD5 and CD20 (and CD19) - like SLL and CLL! Genetics: - 11;14 translocations (30 to 40%) - Do you remember what was on Cr. 14? ---\> IMMUNOGLOBULIN HEAVY CHAIN!! - What gets translocated there? ---\> CYCLIN D! What does over expression of CYCLIN D do? --\> PHOSPHORYLATES the regulators which makes the cell cycle to go from G1 to S facilitating neoplastic proliferation.

Question 13

T cell Leukemia/Lymphoma - neoplastic proliferation of mature ____+ T cells - Occurs with ____-__ infection - RNA virus - Infects ___+ T cells Epidemiology: - endemic in___, ___ and ___. Presentation: - ____ - _____ - _____ - ___ ____ (ulcers, nodules, papular rash) - Rapidly ___ symptoms --\> fatal within months! - If you see __ ___ LESIONS WITH HIGH ___ LEVELS on an exam, don't jump to __ __. Remember, TCL will also presents the same way, except TCL its also have a ____!!!!! Lab Findings: - key diagnostic test: ____ antibodies Note: Patients with ___ ___ also have lytic bone lesions with high ___ levels. Do not confused this though with T cell Leukemia/Lymphoma. MM patients DO NOT have __ __, or __ __ and no ___

Accepted Answer

T cell Leukemia/Lymphoma - neoplastic proliferation of mature CD4+ T cells - Occurs with HTLV-1 infection - RNA virus - Infects CD4+ T cells Epidemiology: - endemic in JAPAN, CARRIBEAN and W. AFRICA Presentation: - LYMPHADENOPATHY - LYMPHOCYTOSIS - HEPATOSPLENOMEGALY - SKIN LESIONS (ulcers, nodules, papular rash) - Rapidly PROGRESSIVE symptoms --\> fatal within months! - If you see LYTIC BONE LESIONS WITH HIGH CALCIUM LEVELS on an exam, don't jump to MULTIPLE MYELOMA. Remember, TCL will also presents the same way, except TCL its also have a RASH!!!!! Lab Findings: - key diagnostic test: ANTI HTLV-1 antibodies Note: Patients with MM also have lytic bone lesions with high CA2+ levels. Do not confused this though with T cell Leukemia/Lymphoma. MM patients DO NOT have SKIN RASH, or LYMPHADENOPATHY and no LYMPHOCYTOSIS

Leukemia Flashcards

(25 cards)