HL Flashcards

(13 cards)

1
Q

Malignancy of mature B lymphocytes

A

Hodgkin’s Lymphoma

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2
Q

4 Histologic subtypes of HL

A

1. Nodular sclerosis – most common in young adults (US)
2. Mixed cellularity
3. Lymphocyte-rich
4. Lymphocyte-depleted

nodular sclerosis + mixed cellularity = ~95% of cases

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3
Q

Diagnostic cell of cHL

A

**Reed-Sternberg (HRS) **

Large cell
Abundant cytoplasm
Bilobed or multinucleated nucleus

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4
Q

Detected in 20–40% of all HL

~100% of HIV-associated cHL

A

Epstein-Barr virus (EBV)

EBV genomes are episomal & clonal → supports role in early lymphomagenesis

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5
Q

Rare cyclic fever pattern in HL

A

PEL EBSTEIN FEVER

days–weeks of fever – afebrile interval – recurrence

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6
Q

STANDARD FOR STAGING

more sensitive than bone marrow biopsy

bone marrow involvement is patchy in cHL

A

PET/CT scan

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7
Q

Tumor features of HL

A

rare malignant B cells (Reed-Sternberg cells)

immunoglobulin genes rearranged but not expressed

background of polyclonal inflammatory infiltrate

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8
Q

Treatment of HL

A

HIGHLY CURABLE
chemotherapy alone or chemotherapy + radiotherapy

ADVANCED-stage disease:
No benefit from routine radiotherapy

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9
Q

EARLY-STAGE cHL (Stage I–II)

A

ABVD (doxorubicin, bleomycin, vinblastine, dacarbazine)

given every 2 weeks
1 cycle = 2 treatments

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10
Q

ADVANCED-STAGE cHL (Stage III–IV)

A

ABVD ×6 cycles

NO ROUTINE RADIOTHERAPY AFTER COMPLETE RESPONSE

RADIOTHERAPY INCREASES RISK OF:
secondary malignancies
thyroid disease
premature cardiovascular disease and stroke

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11
Q

RELAPSED cHL

A

Salvage chemotherapy → autologous stem cell transplant (ASCT)

Cure rate: >50% if chemo-sensitive

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12
Q

COMMON SALVAGE REGIMENS

A

ICE (ifosfamide, carboplatin, etoposide)

GND (gemcitabine, vinorelbine, doxorubicin)

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13
Q

MC presentation of HL

A

FEVER

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