LN, Spleen & Thymus Flashcards

1
Q

define

  • lymphadenopathy
  • lymphadenitis
  • lymphoid hyperplasia
A
  • lymphadenopathy - lymph node swelling
  • lymphadenitis - infection of the lymph nodes
  • lymphoid hyperplasia - reactive increase in lymphocytes in lymph nodes
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2
Q

differences between acute and chronic lymphadenitis

A
  • acute: swelling + redness + TENDERNESS
  • chronic: slow swelling + NONTENDER
    • tends to affect inguinal & axillary lymph nodes more, which drain the extremities & thus receive infections
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3
Q

what are the main morphological patterns of lymphoid hyperplasia?

A
  • follicular
  • paracortical
  • sinus
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4
Q

lymphoid hyperplasia - follicular pattern

  • causes?
  • microscopic morphology?
A
  • causes - bacterial > RA, some viral infections
  • morphology
    • variably sized follicles with
      • asymmetric mantels
      • large, oblong germinal centers that themselves are composed of two regions:
        • dark zone = centroblasts: proliferating blast like B-lymphocytes)
        • light zone = centrocytes: irregular, cleaved lymphocytes
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5
Q

lymphoid hyperplasia - parafollicular pattern

  • causes?
  • microscopic morphology?
A
  • causes - acute viral infections > some medications
  • microscopic morphology: diffuse expansion of T-lymphocytes with some activated T-lymphocytes that are 3-4x larger than others
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6
Q

lymphoid hyperplasia - sinus pattern

  • causes
  • microscopic morphology
A

aka histiocytosis

  • causes: lymph nodes that are draining tumor cells > whipple disease
  • morphology:
    • hyperplasia / hypertrophy of cells lining lymphatic sinusoids + presence of numerous macrophages (histiocytes)
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7
Q

rosai-dorfman disease

  • cause
  • microscopic morphology
  • clinical presentation
A
  • cause: type of sinus lymphoid hyperplasia
  • microscopic
    • sinuses markedly dilated, and filled with histiocytes (macrophages) that have ingested other WBCs = emperipolesis
  • clinical
    • m/c in children/young adults
    • massive bilateral cervical lymphadenopathy*
    • fever, night sweats, weight loss
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8
Q

granulomatous lymphadenopathy

  • causes
  • microscopic morphology
A
  • two types:
    • necrotizing granulomas:
      • common causes
        • TB
        • animal carried - catch scratch, tularemia, histoplasmosis
    • non-caseating granulomas
      • common causes - numerous, but watch out for sarcoidosis
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9
Q

metastatic tumors to lymph nodes

  • pathogenesis
  • microscopic morphology
A

tumor cells enter afferent lymphatics, which feed into the medullary (subcapsular) sinus → medullary sinuses → medulla → cortex

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10
Q

identify picture, note important features

A

lymphoid hyperplasia - follicular pattern (bacterial)

follicle w/ asymmetric mantels + large, oblong germinal centers made of dark zone (centroblasts) & light zone (centrocytes)

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11
Q

identify picture, note important features

A

lymphoid hyperplasia - parafollicular pattern (acute viral)

T-lymphocytes with some activated T-lymphocytes that are 3-4x larger than others

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12
Q

identify picture, note important features

A

lymphoid hyperplasia - sinus pattern

increase #/size of cells lining sinusoids + numerous macrophages (histiocytes)

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13
Q

identify the picture, note important features

A

rosai-dorfman disease - sinus histiocytosis with massive lymphadenopathy

marked dilation of sinuses + intrasinusoidal histiocytes

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14
Q

identify picture, note important features

A

rosai-dorfman disease - sinus histiocytosis with massive lymphadenopathy

emperipolesis: intrasinusoidal histiocytes (macrophages) that have ingested other WBCs

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15
Q

identify picture, note important features

A

necrotizing granuloma

commonly caused by TB or animal-host diseases: cat scratch, tularemia, histoplasmosis

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16
Q

identify picture, note important

A

non-necrotizing granulomas

common causes - many, look out for sarcoid

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17
Q

identify the picture, note important features

A

metastatic tumor to lymph nodes

tumors cells travel: marginal sinus → medullary sinuses → medulla → cortex

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18
Q

accessory spleen

  • cause
  • morphology
  • clinical significance
A
  • cause - congenital
  • morphology
    • histology - normal & function normal
    • gross - can be anywhere in the abdomen
  • clinical:
    • in 20-35% of normal persons
    • clinically insignificant, except for the cases in which a splenectomy is necessary as tx: then must also remove accessory spleen
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19
Q

asplenia

  • morphology
  • clinical significance
A
  • cause - congenital
  • morphology - absent spleen
  • clinical - often associated with heart abnormalities
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20
Q

splenic granulomas

  • cause
  • morphology
A
  • cause - fungal infections > sarcoidosis, Hodgkin’s & non-Hodgkin’s lymphoma
  • morphology - see picture
21
Q

perisplenitis

  • cause
  • morphology
  • clinical significance
A
  • cause - multiple rounds of inflammation of the splenic capsule
  • morphology - thick white fibrous & plaques (made of collagen) coat the the splenic surface
  • clinical - incidental finding at biopsy
22
Q

splenic insufficiency

  • cause
  • morphology
  • clinical significance
A
  • cause - splenectomy: either
    • surgical
    • auto: d/t sickle cell disease (causes infraction)
  • morphology - n/a
  • clinical - pts w/ insufficiency must be vaccinated against encapsulated bacteria:
    • s. pneumonia
    • m. meningitis
    • h. influenza
23
Q

splenomegaly - causes

A
  • hematogenous disorders - MPNs, hodgekins & non-hodgekins
  • primary splenic neoplasms
  • hemolytic anemia
  • autoimmune disease
  • infections
  • congestive states
  • hemophagocytic lymphohistiocytosis
24
Q

splenomegaly - morphology

A
  • gross -
    • enlarged & firm
    • outer surface; with thickened & fibrous capsule
    • cut surface: homogenous, beefy red congested red pulp d/t hemorrhagic that becomes → fibrotic
25
Q

congestion leading to splenomegaly

  • pathogenesis?
  • morphology?
  • clinical presentation?
A
  • pathogenesis: d/t venous outflow obstruction
    • often liver related:
      • intrahepatic disorders - cirrhosis
      • extra-hepatic disorders - hepatic → portal → splenic veins
  • morphology
    • gross:
      • outer surface - enlarged firm
      • cut surface - red, congested
    • microscopic:
      • hypocellular + hemorrhagic
        • with dilated sinuses
  • clinical - evolves to hypersplenism → pancytopenia
26
Q

hemophagocytic lymphohistiocytosis leading to splenomegaly

  • pathogenesis?
  • morphology?
  • clinical presentation?
A
  • pathogenesis:
    • m/c caused by infection - esp EBV & HIV. infections activate macrophages, which phagocytose blood cells (progenitors & mature)
  • morphology
    • gross: splenomegaly
    • microscopic: macrophages that have phagocytized lymphocytes in splenic sinuses (like in rosai-dorfman disease)
  • clinical - cytopenia, which can evolve to → DIF / shock / multi-organ failure
27
Q

splenic rupture

  • m/c causes
  • sequelae
A
  • causes:
    • m/c - trauma, surgical intervention
    • also - spontaneous (but only in abnormal spleens)
  • life threatening hemorrhage → splenic implants
28
Q

what are the benign tumors of the spleen?

A
  • hemangioma
  • lymphangioma
29
Q

hemangioma

  • morphology
  • clinical relevance
A
  • morphology
    • < 2 cm
    • usually of cavernous type
  • clinical relevance - most common primary tumor of the spleen
30
Q

lymphangioma

  • morphology
  • clinical relevance
A
  • morphology:
    • tend to be subscapular region
    • lumina contain proteinaceous material
  • clinical relevance
    • mostly seen in children
31
Q

what are the malignant tumors of the spleen?

A

angiosarcoma

32
Q

angiosarcoma

  • morphology
  • clinical relevance
A
  • morphology: either single nodular, or diffuse
  • clinical relevance: m/c non-lymphoid malignant neoplasm of the spleen
33
Q
A

accessory spleen

can be found anywhere in the abdomen

34
Q
A

perisplinitis

thick white fibrous & plaques (collagen) on splenic surface d/t multiple rounds on inflammation to the capsule

35
Q
A

slenomegaly

  • congested, red pulp that becomes fibrotic over time
36
Q
A

hemophagocytic lymphohistiocytosis → congestion

activated macrophages stuffed w/ lymphocytes

37
Q
A

splenic rupture

38
Q

what are the most common sites of metastasis to the spleen?

A
  • melenoma
  • lung
  • breast
  • gastric
  • pancease
  • liver
  • colon
39
Q
A

lymphangioma (benign splenic tumor)

lumina containing proteinaceous material instead of RBCs

40
Q

acute thymic involution

  • cause
  • morphology
A
  • cause - extreme metabolic stress (high cortisol levels)
    • malnutrition
    • chronic infections
    • immunodeficiency
    • premature / ill term infants
  • morphology - inc lymphocyte death
41
Q

what are the causes of

  • thymic hypoplasia?
  • thymic hyperplasia?
A
  • thymic hypoplasia - Di George syndrome
  • thymic hyperplasia - myasthenia gravis
42
Q

thymoma - clinically features, significance?

A
  • arise in middle age
  • M= F
  • most are benign
  • often associated with hyperplastic thymic syndromes (unless thymic carcinoma)
  • most common primary anterior mediastinal tumor
43
Q

thymoma - morphology

A
  • gross - lobulated, encapsulated mass
  • microscopic - either:
    • spindle type
    • epithelioid type
    • mixed type
44
Q

what are the malignant thymomas?

what are the features of each?

A
  • invasive thymoma
    • benign cytological features
    • but, invades thru capsule
  • thymic carcinoma
    • malignant cytological features (m/c SSC)
    • NOT associated with myasthenia gravis
45
Q
A

benign thymoma - tan, lobulated & encapsulate mass

m/c primary anterior mediastinal neoplasm

46
Q
A
47
Q
A

acute thymic involution - loss of lymphocytes d/t metabolic stress

(in this case - cortex loss)

48
Q
A

thymic hyperplasia (myasthenia gravis)