Abdomen Flashcards

(38 cards)

1
Q

Causes of end stage renal disease

A

Polycystic kidney disease
Diabetes mellitus
Hypertension
Glomerulonephritis
Autoimmune condition
Alport disease

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2
Q

Barrier to kidney transplantation

A

Severe obesity
Active or recent malignancy
Ongoing deep seated infection
Active vasculitis

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3
Q

Long term effect of immunosuppresion

A

Opportunistic infection
Malignancy, skin malignancy
Steroids : thinning of skin, easy bruising, Cushingnoid apperancmd
Cyclosporine : gingival hyperplasia and renal impairment
Tacrolimus : tremor, new onset diabetes, nephrotoxicity

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4
Q

Crohn’s Disease

A

Transmural disease
Non casseating granuloma
Fistula and fissuring
Non - bloody diarrhea
Weight loss
Abdominal pain
Peri anal disease - ulcer, skin tag
Extra - intestinal manifestation
Complications : small bowel cancer, colorectal ca, osteoporosis

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5
Q

Extra intestinal manifestation of crohn’s disease

A

A - Arthritis
C - Clubbing
E - Episcleritis, erythema nodosum,
P - Pyoderma gangrenosum, primary sclerosing cholangitis
O - Osteoporosis, oral ulcer

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6
Q

Investigation of crohn’s disease

A

Fbc
Raised Crp
Raised Esr
Low B12 and vitamin d
Faecal calprotectin
X Ray : rose thorn apperance
Colonoscopy : cobblestone appearance, deep ulcer, skip lesion, fistula

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7
Q

Bilateral ballotable kidney

A

Adpkd
Bilateral rcc
Bilateral obstructive uropathy
Vhl
Tsc
Amyloidosis
Infilrative disease

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8
Q

Unilateral ballotable kidney

A

Pyelonephritis
Hydronephrosis
Rcc
Peri renal hematoma
Renal hyperplasia post nephrectomy
Adpkd with Unilateral enlargement

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9
Q

Why is this a ballotable kidney?

A

Ballotable and move with respiratory
Can get above swelling
Percussion on it is resonance

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10
Q

Causes of abdominal pain in transplanted kidney

A

Graft rejection
Graft thrombosis
Graft infection
Renal stone
Ureteric obstruction
Gastritis / pud from steroids

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11
Q

Causes of graft tenderness

A

Graft infection
Graft rejection
Graft thrombosis

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12
Q

Fever in transplanted kidney

A

Opportunistic infection
Malignancy
Uti/pyelonephritis
Fistula infection

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13
Q

Anemia + jaundice + hepatosplemomegaly

A

Myeloproliferative disease
Lymphproliferative disease
Chronic hemolytic anemia
Infection : hiv, disseminated tb, infective mononeuclosis

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14
Q

Typical features of hemolytic anemia

A

Anemia
Jaundice
Splenomegaly

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15
Q

Confirm of hemolytic anemia

A

Hb electrophoresis
High reticuloytes count
Fbc with pbf
High serum billirubin
Skeletal survey
Serum iron : high ferritin, high iron, low tibc

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16
Q

Young tender hepatomegaly

A

Viral hepatitis
Liver abcess
Alcoholic hepatitis
Budd chiarri syndrome

17
Q

Isolated splenomegaly

A

Myeloproliferative disease
Lymphproliferative disease
Infection (hiv, malaria)
Hemolytic anemia

18
Q

Why is this an enlarged spleen?

A

Move toward right illiac fossa
Cannot get about the spleen (below costal margin)
Not ballotable
Dull on percussion
Presence of splenic notch

19
Q

Post splenectomy precautions

A

Vaccination 2/52 prior splenectomy (hemophillus, pneumococcal, meningococcal)
Medical bracelet
Lifelong peniclin

20
Q

Complications of thalassemia

A

Extramedullary hemopoiesis
- hepatosplemomegaly, frontal bossing, maxillary prominence
Heart failure
- anemia causing high output heart failure
- restrictive cardiomyopathy secondary to iron overload
Iron overload
- hemochromatosis - > chronic liver disease + stigmata of cld + bronze skin appearance
- bronze DM : finger prick mark, dermopathy, insulin site
- pseudogout
- hypogonadotrophic hypogonadism: loss of axillary hair, short stature, testicular atrophy, amenorrhea
Chronic hemolysis
- cholelithiasis/ cholecystectomy
- splenomegaly/ splenectomy
- transfusion dependent

21
Q

Indication of splenectomy

A

Hypersplenism - massive spleen/ rupture/ pain
High transfusion requirement - > 250ml/kg/ year or doubling of volume per year
Splenic infact/ splenic vein thrombosis

22
Q

Investigation for thalassemia

A

Fbc (to look for anemia)
Fbp (to look for target cell)
Rp / lft
Hemolytic workup
Hb electrophoresis
Complications
- pituitary hormone screening
- metabolic : fbs / Hba1c
- hemochromatosis : mri t2* (heart/ liver)
- hepatitis (regular transfusion)
- dexa scam
- us abdomen
-

23
Q

Investigation for thalassemia

A

Fbc - look for anemia
Fbp - look for target cell
Hb electrophoresis and dna analysis - to confirm diagnosis
Rp and lft
Complications
- metabolic : fbc/Hba1c
- pituitary panel
- iron overload (mri t2* - heart and liver)
- hepatitis panel
- echo
- osteoporosis : dexa scan

24
Q

Management of thalassemia

A

MDT
Patient education and counselling
Dietitian - low iron / high protein diet
Annual vaccination

Pharmacology
Regular transfusion (aim hb >10)
Iron chelating - evidence of overload
Bone protective agents
Monitor bp / sugar/ cholesterol

Surgical
Splenectomy
Cholecystectomy
Hsct

25
Myeloproliferative disease
Cml Polythemia rubra Vera Myelofibrosis Essential thrombocythemia
26
Lymphadenopathy + hepatosplemomegaly
Lymphproliferative disease (cll, lymphoma) Disseminated tb Im Cmv Hiv Sle Sarcoidosis
27
Investigation
Usg abdomen Lymph node biopsy Tb - > sputum afb, cxr Viral screening Ctd screening
28
Post splenectomy fbp
Howell Jolly body Spherocytes Target cell
29
Causes of hepatomegaly in thalassemia patient
Extramedullary hemopoiesis Secondary hemothochromatosis Hepatitis secondary to regular transfusion
30
Hepatosplenomegaly Clubbing J scar Anemia
Post transplant Lymphproliferative disorder Chronic liver disease with portal hypertension Infective endocarditis Granulomatous infection Hematological malignancy (myelofibrosis, lymphoma)
31
Abdominal causes of clubbing
Primary biliary cholangitis Primary sclerosing cholangitis Chronic liver disease with portal hypertension Ulcerative collitis Coeliac disease Gi lymphoma
32
Abdominal pain in ADPKD
Acute hemorrhage in the cyst Infection in the cyst Renal stone
33
Unconscious patient in ADPKD
Subarachnoid hemorrhage (rupture of berry aneurysm) Htn complication Hyponatremia
34
Inheritance of APDKD
Autosomal dominant ADPKD 1 = Chromosome 16 ADPKD 2 = Chromosome 4
35
Normal liver span
6 - 12 cm from midclavicular line
36
Portal hypertension in cld
Hepatic encephalopathy Splenomegaly Esophageal varies Ascites Caput medusa
37
Decompensation in chronic liver disease
Altered consciousness - hepatic encephalopathy Altered colour - jaundice Asterexis Ascites
38
Causes of decompensation
Bleeding Constipation Drugs - toxin, alcohol Dehydration Electrolyte imbalance Infection