Kebbekus IHO Week 4 Flashcards

1
Q

Typical presentation of Hodgkins Lymphoma

A

enlarging, rubbery, but not tender lymphadenopathy; typically in the neck or chest

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2
Q

Symptoms that can accompany Hodgkins Lymphoma

A

fatigue, fever, weight loss, night sweats, pain with EtOH, sx of cytopenias, hepatosplenomegaly, pruritis

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3
Q

malignant cell is Reed-Sternberg cell, now recognized as a B-cell some are CD20+, bulk of the tumor is reactive tissue, spreads contiguously from node to node

A

Hodgkin Lymphoma

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4
Q

CD30+, nodular sclerosis (grades I and II), lymphocyte-rich classical, mixed cellularity, lymphocyte depleted

A

Classical HL (WHO)

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5
Q

CD20+

A

Nodular Lymphocyte Predominant (WHO)

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6
Q

Staging Lymphomas A

A

no systemic symptoms

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7
Q

Staging Lymphomas B

A

fever, night sweats, weight loss

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8
Q

Staging Lymphomas E

A

extralymphatic site

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9
Q

Staging Lymphomas S

A

splenic disease

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10
Q

Localized favorable risk disease treatment

A

ABVD x 2

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11
Q

Stage 3 and 4 Disease

A

ABVD x 2 (restage), ABVDx4, +/- XRT, ABVDx2 (restage-refractory) intense chemotherapy BEACOPP, autologous transplant

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12
Q

Late Effects of Therapy-Second Malignancy

A

solid tumors (lung and breast cancer) and secondary leukemia, heart disease, lung disease, impaired fertility

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13
Q

IPI Scoring System Prognostic Factor

A

age over 60, stage 3 and 4, ECOG PS (eastern cooperative oncology group performance status) 3 or 4 more than 1/2 day resting, elevated LDH, 2 or more extranodal sites

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14
Q

Average age of onset of Diffuse Large B-cell Lymphoma

A

67 (75% over age 55)

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15
Q

what is the prototype aggressive NHL of adults

A

Diffuse Large B-cell Lymphoma

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16
Q

most common indolent NHL, that accounts for 22% in North America and is rare in Asia

A

Follicular Lymphoma

17
Q

This is typically advanced at presentation and is often aymptomatic and NOT curable

A

Follicular Lymphoma

18
Q

Cytogenetics of Follicular Lymphoma

A

t(14;18)(q32;q21)
BCL-2 chromosome 18q21 inhibits apoptosis
IgH chromosome 14q32

19
Q

Treatment of Indolent NHL

A

Only when forced to: pushy nodes (hydrophephrosis, jaundice, dysphagia/stridor), cytopenias (bone marrow failure), B symptoms or fatigue

20
Q

Risk of treating NHL?

A

transformation to aggressive lymphoma

21
Q

frequently H.pylori associated, tx with 2-3 rounds of eradication, time between EGDs, if no clearing of MALT after 2-3 courses then radiation and/or chemo and/or rituximab, ds outside the stomach or diffuse large cell transformation–chemotherapy

A

MALT Lymphoma

22
Q

NHL Indolent (follicular, MALT, marginal zone, SLL) survival, curability and to tx or no?

A

years, generally not curable, defer tx until sx

23
Q

NHL Aggressive (DLBC, Mantle Cell) survival, curability and to tx or no?

A

months, curable in some, treat

24
Q

NHL Very Aggressive (lymphoblastic Burkett, Aids related) survival, curability and to tx or no?

A

weeks, curable in some, tx

25
Q

Hodgkin Lymphoma all types survival, curability and to tx or no?

A

variable (months to years), curable in most, treat

26
Q

What is the prototype of T cell lymphomas?

A

Mycosis fungoides

27
Q

What are the general principles of T cell lymphomas?

A

not curable, frequentl relapse but systemic involvement is uncommon, treatment is UV light radiation, topical or systemic

28
Q

First line of treatment for Systemic T cell lymphoma?

A

CHOP (NOT rituximab); if CD30+ then brentuximab vedotin as targeted therapy

29
Q

What to use to tx Hodgkins?

A

ABVD: adriamycin, bleomycin, vinblastine and dacarbasine (not lung toxicity of bleomycin)

30
Q

Chlamydia psittaci

A

Ocular adnexa; MALT