Patho week 4 Flashcards

(47 cards)

1
Q

Enlargement of lymph node

A

Lymphadenitis

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2
Q

Regions affected in acute non specific lymphadenitis

A

Cervical: infections of teeth or tonsils
Axillary or inguinal: infections in extremities
Mesenteric: acute appendicitis

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3
Q

How are the nodes in acute non specific lymphadenitis

A

Swollen, gray-red and engorged

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4
Q

Characteristics of chronic non specific lymphadenitis

A

Lymph nodes are nontender
In inguinal and axillary nodes

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5
Q

Immune response of follicular and paracortical hyperplasia

A

Follicular: humoral immune respones (macrophages)
Paracortical: T-cell immune response (immunoblasts)

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6
Q

Characteristics of reticular hyperplasia

A

Increase in number an size of endothelial cells lining lymphatic sinusoids

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7
Q

Most common indolent form NHL

A

Follicular lymphoma

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8
Q

Translocation of follicular lymphoma

A

t(14:18) → overexpression BCL2

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9
Q

Predominant cell in follicular lymphoma

A

Centrocytes → small cells with irregular cleaved nuclear contours and scant cytoplasm

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10
Q

Immunophenotype of follicular lymphoma

A

Express CD19, CD20, CD10, surface Ig, BCL6
Do not express CD5
BCL2 expressed in 90% cases

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11
Q

Mutation in diffuse large cell lymphoma

A

Somatic hypermutation that results in overexpression of BCL6

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12
Q

Waldeyer ring is commonly involved in this lymphoma

A

Diffuse large cell lymphoma

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13
Q

Morphology of diffuse large cell lymphoma

A

Large cell size and diffuse pattern of growth

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14
Q

Immunophenotype of diffuse large cell lymhpoma

A

Express CD19 and CD20
Variable expression of CD10 and BCL6

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15
Q

One of the fastest-growing human tumors that predominates in children and young adults

A

Burkitt lymphoma

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16
Q

Morphologic characteristic of Burkitt lymphoma

A

Starry sky

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17
Q

Mutation in Burkitt lymphoma

A

Translocations MYC gene (chromosome 8)

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18
Q

Immunophenotype of Burkitt lymphoma

A

Express IgM, CD19, CD20, CD10, BCL6
Does not express BCL2

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19
Q

Main characteristic of Hodgkin lymphoma

A

Reed-Sternberg cells

20
Q

Classification of Hodgkin lymphoma

A

Classical: nodular sclerosis, mixed cellularity, lymphocyte-rich, lymphocyte depletion
Nodular lymphocyte predominance

21
Q

Characteristics of nodular sclerosis in HL

A

Most common
Good prognosis
Lacunar cells with mixed infiltrate
Deposit of collagen bands

22
Q

Characteristics of mixed cellularity in HL

A

Mix of inflammatory cells
70% EBV+ and RS
Common older males
Good prognosis

23
Q

Characteristics of lymphocyte-rich in HL

A

Uncommon
Reactive lymphocytes in background with RS
Very good/excellent prognosis

24
Q

Characteristics of lymphocyte depletion in HL

A

Least common
Abundant RS and paucity of lymphocytes
Older adults
Bad prognosis

25
Characteristics of nodular lymphocyte predominance in HL
Good prognosis No RS cells Small lymphocytes and macrophages CD20 and BCL6
26
Origin of Reed-Sternberg cells
Originate from germinal center
27
What does classical HL activate
NF-kB
28
Clinical features in multiple myeloma
Calcium elevation Renal failure Anemia Bone lesions
29
Epidemiology of multiple myeloma
Men and Africans 65-70 years old
30
Pathogenesis of multiple myeloma
IGH locus rearrangement in 14q32 and cyclin D1a and D3
31
IL that ensures proliferation and survival of multiple myeloma
IL-6
32
Morphology of multiple myeloma
Destructive plasma cell tumors (plasmacytomas) involving axial skeleton
33
Bones more commonly affected in multiple myeloma
Vertebral column, ribs, skull, pelvis, femur, clavicle, scapula
34
Macroscopic morphology of bone lesions in multiple myeloma
Soft, gelatinous, red tumor masses
35
Cytologic variants in multiple myeloma
Plasmablasts: single prominent nucleolus Multinucleated/bizarre cells Flame cells: fiery red cytoplasm Mott cells: grapelike cytoplasmic droplets Russell bodies: cytoplasmic inclusions Dutcher bodies: nuclear inclusions
36
Immunophenotype of multiple myeloma
CD138+, syndecan-1, CD56+
37
Main complication of multiple myeloma
Renal failure → Bence Jones proteinuria
38
Prognosis of multiple myeloma
Good prongosis: Cyclin D1 translocation Bad prognosis:13q or 17p deletions, t(4:14)
39
Most common mutation in Langerhans cell histiocytosis
Valine-to-glutamate substitution at residue 600 in BRAF
40
Pathogenesis of Langerhans cell histiocytosis
Expresses both CCR6 and CCR7 (rather than just CCR6) → allows neoplastic cells to migrate into tissues and express chemokines
41
Chemokines released in Langerhans cell histiocytosis
CCL20 in skin and bone CCL19 and CCL21 in lymphoid organs
42
Morphology of Langerhans cell histiocytosis
Langerhan cells: many, vacuolated cytoplasm and vesicular nuclei containing linear grooves or folds Birbeck granules in cytoplasm: has langerin
43
Characteristics of multifocal multisystem Langerhans cell histiocytosis
Letterer-Siwe disease <2 years old Development cutaneous lesions resembling seborrheic eruption in trunk and scalp
44
Characteristics of unifocal and multifocal unisystem Langerhans cell histiocytosis
Eosinophilic granuloma Proliferations of Langerhans cells admixed with eosinophils, lymphocytes, plasma cells and neutrophils Arises within medullary cavities of bones (calvaria, ribs, femur)
45
Difference between unifocal and multifocal unisystem Langerhans cell histiocytosis
Unifocal: older children and adults Multifocal: children
46
Hand-Schüller-Christian triad
Calvarial bone defects, diabetes insipidus and exophthalmos
47
Who is affected by pulmonary Langerhans cell histiocytosis
Adult smokers