Lymphomas and Multiple Myeloma Flashcards

1
Q

____ are dense collections of
immune cells that filter antigens from extracellular fluid passing through

A

Lymph nodes

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2
Q

_____: disease of a lymph node

A

Lymphadenopathy

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3
Q

Lymphadenopathy:

A

disease of a lymph node
○ It reflects disease secondary to an increase in normal lymphocytes and macrophages in response to an antigen

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4
Q

Enlarged Lymph Node causes

A

● Lymphadenopathy
● Most often due to benign, self-limited conditions, such as viral
infections
● Other causes include accumulation of cells in response to an infection in the node itself (lymphadenitis), metastatic malignancy, or neoplastic
lymphocytes (lymphoma)

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5
Q

Tenderness of lymph nodes suggests _____

A

acute inflammation, the kind that
comes with localized or acute infections

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6
Q

If your patient reports lymphadenopathy of a few days or even a couple of weeks, it is appropriate to _____

A

wait for 3-4 weeks to see if it
resolves before arranging further workup

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7
Q

f your patient comes in reporting a swollen lymph node
that is _____, assess for signs concerning for malignancy

A

non-tender and has been present for a couple of
weeks

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8
Q

Lymph nodes ____ cm or greater are more concerning for malignancy

A

2

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9
Q

Good initial imaging for lymphadenopathy

A

Ultrasound

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10
Q

Types of biopsy on lymphadenopathy if malignancy is possible

A

○ Fine Needle Aspiration Biopsy: Less invasive but has the potential to miss the pathology within the node itself
○ Excisional Biopsy: Most ENT and General Surgeons prefer to remove the entire node to establish a more certain diagnosis

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11
Q

The lymphomas are often referred to as the “wet cancers” because ____

A

they can infiltrate any tissue

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12
Q

Lymphomas are generally categorized as

A

● Hodgkin Lymphoma: A specific type of cancer
● Non-Hodgkin Lymphomas: A large group of several types of Lymphoma

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13
Q

Hodgkin Lymphoma age distribution

A

bimodal age distribution: 20s and 50s

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14
Q

About 85% of children who develop Hodgkin’s are ____

A

male

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15
Q

Inheritance pattern of hodgkins?

A

No consistent chromosomal or hereditary pattern of inheritance
has been established
Also called “Hodgkin’s Disease”

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16
Q

Hodgkin Lymphoma Pathophysiology

A

● A malignant disease of the lymph tissue (lymph cancer)
● Characterized by the presence of
Reed-Sternberg cells
● The disease tends to start in a localized region of lymph nodes and then spreads in an orderly, predictable fashion to adjacent sites
of lymph tissues

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17
Q

S/S of hodgkins lymphoma

A

● Painless lump in neck area
● Fevers/chills
● Night sweats
● Weight loss
● Anorexia
● General malaise
● Intermittent pruritus

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18
Q

Some people with Hodgkin will experience pain/soreness at lymph node with ____ ingestion

A

ETOH (alcohol)

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19
Q

Pel-Ebstein pattern is sometimes seen with

A

Hodgkin lymphoma
Days or weeks of febrile period alternating with days or weeks of afebrile period

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20
Q

Excisional biopsy is
____ over FNA for diagnosis of _____

A

preferred; hodgkin lymphoma

21
Q

Laboratory tests in hodgkin lymphoma may show:

A

○ Normocytic anemia (if bone marrow infiltration)
○ Elevated erythrocyte sedimentation rate (ESR)
○ Mild leukocytosis with decreased lymphocytes

22
Q

Other imaging for hodgkin lymphoma

A

● Chest X-ray may show mediastinal lymphadenopathy
● CT chest/abdomen/pelvis required for staging
○ PET scan often used in the initial staging too

23
Q

Hodgkin lympoma treatment

A

● General surgeon or ENT surgeon for biopsy
● If diagnosis is established, contact oncology right away to set up
consultation
● Treatment could include chemotherapy, chemo and radiation combo, and possible stem cell transplant

24
Q

Ann arbor staging

A

○ Stage I - one nodal area/region
○ Stage II - two areas on one side of diaphragm
○ Stage III - both sides of diaphragm
○ Stage IV - disseminated; disease within bone marrow or liver
○ Addition of A - lacks constitutional symptoms
○ B- 10% weight loss over 6 months, fever, and night sweats

25
Q

General treatment guidelines and prognosis by stage for Hodgkin lymphoma

A

■ Stages I, II, and IIIA - Radiation therapy
■ Stages IIIB, IV - Combination chemo, with or without
radiation therapy
■ 5 year survival rate for Stage I is >95%
● For Stage IV, about 65%

26
Q

Non-Hodgkin Lymphomas (NHLs)

A

A group of dozens of forms of Lymphoma all
classified as Non-Hodgkin Lymphomas
(Non-Hodgkin’s Disease)
○ Classified functionally as B-cell or T-cell

27
Q

Median age of diagnosis for NHLs

A

Median age at diagnosis is 50 years of age
○ Does occur fairly often in pediatric
population
○ Incidence possibly increases with age as well

28
Q

Non-Hodgkin is much ____
common than Hodgkin

A

more

29
Q

S/S NHLs

A

painless, peripheral lymphadenopathy
○ Unlike Hodgkin’s, NHL
lymphadenopathy seems to be more generalized rather than localized to one region
○ ⅔ have retroperitoneal, mesenteric, or pelvic nodal involvement
● Extranodal involvement can occur (GI, skin, CNS, etc)

30
Q

Constitutional symptoms (fever, chills, night sweats, weight loss)
can occur, but are much ____ common in NHL

A

less

31
Q

Non-Hodgkin Lymphoma diagnosis

A

● Tissue biopsy is required for definitive diagnosis
● Peripheral blood smear is usually normal, even with extensive bone
marrow involvement
● Disease is usually already disseminated at time of diagnosis

32
Q

Plasma Cells are specialized Lymphocytes that simply excrete large amounts of ____ at their activation

A

whatever antibody they were programmed to create

33
Q

When a B-Lymphocyte is activated, it differentiates into a
_____

A

more specialized, mature version of B-Lymphocyte

34
Q

Multiple Myeloma

A

● MM is malignant proliferation of a
single clone of Plasma Cell
○ Resulting in excess monoclonal
paraproteins (M protein)

35
Q

MM epidemiology

A

● Most commonly seen in older adults
○ Most are in their 60s or 70s
● More common in men than women
● Exposure to radiation, benzene, and pesticides may play a role based on recent research

36
Q

Multiple Myeloma pathophysiology

A

● One rogue Plasma Cell starts it off
The malignant cells secrete
● Osteoclast Activating Factor (OAF) which stimulates inappropriate bone breakdown
● The cells also secrete excessive amounts of monoclonal Immunoglobulin protein (M-Protein), and these sometimes form chains that block glomeruli, causing kidney injury

37
Q

Common triad of MM

A

○ Bone pain
○ Anemia
○ Kidney injury

38
Q

Skull or other X-rays may show
punched out lytic lesions in

A

Multiple myeloma

39
Q

Occasionally, clumps of Plasma Cells aggregate in various locations
and become a _____ in ___

A

Plasmacytoma; MM

40
Q

S/S of Multiple Myeloma

A

● Bone pain - 70%
○ Can develop pathologic fractures
● Normocytic anemia
● Thrombocytopenia
● Leukopenia
● Osteopenia
● Hypercalcemia
● Fatigue
● Recurrent Infection

41
Q

BREAK mnemonic for S/S of Multiple Myeloma

A

○ Bone pain: Osteolytic destruction
○ Recurrent infections: From the leukopenia
○ Elevated calcium
○ Anemia
○ Kidney failure

42
Q

Multiple Myeloma on CBC

A

shows normocytic anemia in 80-90% of cases

43
Q

MM CMP findings

A

shows hypercalcemia, possibly elevated BUN/Creatinine,
and elevated total protein
○ High protein because of excess immunoglobulin circulating in
serum

44
Q

Serum Protein Electrophoresis (SPEP) and Urine Protein
Electrophoresis (UPEP) findings for MM

A

show monoclonal protein spike
(M-spike) - Classic, essentially pathognomonic

45
Q

Bone marrow biopsy findings with MM

A

Shows 20-30% Plasma Cells

46
Q

Multiple Myeloma PBS findings

A

may show Rouleaux formation (coin-stacking formation), but not always

47
Q

24 hour urine electrophoresis findings for MM

A

May show Bence-Jones Proteins
(excess free light chains;
M-proteins)

48
Q

Multiple Myeloma Treatment

A

● Although MM is presently incurable, treatment often involves
immunomodulatory agents, chemotherapy, autologous stem cell
transplant, and/or radiation
● Supportive treatments (i.e. Bisphosphonates) have shown some
improvement in delaying skeletal disease and improving bone pain

49
Q

Median survival of Multiple Myeloma

A

● Median survival is 7 years after diagnosis
○ Eventual bone marrow failure