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
**congestion** leading to splenomegaly * pathogenesis? * morphology? * clinical presentation?
* 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
**hemophagocytic lymphohistiocytosis** leading to splenomegaly * pathogenesis? * morphology? * clinical presentation?
* 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
splenic rupture * m/c causes * sequelae
* causes: * m/c - **trauma, surgical intervention** * also - spontaneous (but only in abnormal spleens) * life threatening hemorrhage → splenic implants
28
what are the benign tumors of the spleen?
* hemangioma * lymphangioma
29
hemangioma * morphology * clinical relevance
* morphology * \< 2 cm * usually of cavernous type * clinical relevance - **most common primary tumor of the spleen**
30
lymphangioma * morphology * clinical relevance
* morphology: * tend to be subscapular region * **lumina contain proteinaceous material** * clinical relevance * mostly seen in children
31
what are the malignant tumors of the spleen?
angiosarcoma
32
angiosarcoma * morphology * clinical relevance
* morphology: either single nodular, or diffuse * clinical relevance: m/c non-lymphoid malignant neoplasm of the spleen
33
accessory spleen can be found anywhere in the abdomen
34
perisplinitis _thick white fibrous & plaques_ (collagen) on splenic surface d/t multiple rounds on inflammation to the capsule
35
slenomegaly * congested, red pulp that becomes fibrotic over time
36
hemophagocytic lymphohistiocytosis → congestion activated macrophages stuffed w/ lymphocytes
37
splenic rupture
38
what are the most common sites of metastasis to the spleen?
* melenoma * lung * breast * gastric * pancease * liver * colon
39
lymphangioma (benign splenic tumor) lumina containing proteinaceous material instead of RBCs
40
acute thymic involution * cause * morphology
* cause - **extreme metabolic stress** (high cortisol levels) * malnutrition * chronic infections * immunodeficiency * premature / ill term infants * morphology - **inc lymphocyte death**
41
what are the causes of * thymic hypoplasia? * thymic hyperplasia?
* thymic hypoplasia - Di George syndrome * thymic hyperplasia - myasthenia gravis
42
thymoma - clinically features, significance?
* 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
thymoma - morphology
* gross - lobulated, encapsulated mass * microscopic - either: * **spindle type** * **epithelioid type** * **mixed type**
44
what are the malignant thymomas? what are the features of each?
* invasive thymoma * **benign cytological features** * but, _invades thru capsule_ * thymic carcinoma * **malignant cytological features** (m/c SSC) * _NOT_ associated with myasthenia gravis
45
benign thymoma - tan, lobulated & encapsulate mass **m/c primary anterior mediastinal neoplasm**
46
47
acute thymic involution - loss of lymphocytes d/t metabolic stress (in this case - cortex loss)
48
thymic hyperplasia (myasthenia gravis)