spleen and thymus Flashcards

1
Q

red pulp

A

traversed by numerous thin walled sinusoids separated by cords of billroth
endothelium lining sinusoids discontinuous

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2
Q

cords

A

contain labyrinth of macros loosley connected vi along dendritic processes
physical and functional barrier

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3
Q

open circulation

A

thru capillaries into cords -> sinusoids

only small percentage, but over course of the day filters entire blood volume

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4
Q

closed circuit

A

blood passes rapidly and directly from capillaries into splenic vv

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5
Q

white pulp follciles

A

artery w/eccentric collar of T cells -> periarteriolar lymphatic sheath
at intervals the sheath expands to from lymphoid nodules of B cells which can create germinal centers

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6
Q

functions of spleen

A

phagocytosis of blood cells and particulate matter
Ab production
hematopoiesis
sequestration of formed blood elements

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7
Q

phagocytosis of blood and partciulates

A

red cells that get stuck are phagocytosed by macros

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8
Q

pitting of RBC

A

process by which splenic macros excise inclusions to remove particles such as bacteria from blood

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9
Q

Ab production

A

DCs in periarterial lymph sheath trap Ags present to T cells which activate B cells which mature to Ab producing plasma cells in red pulp

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10
Q

hematopoiesis

A

fetal

compensatory extramedullary

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11
Q

sequestration of formed blood elements

A

splenomegaly can cause an increase in WBCs stored in spleen -> thrombocytopenia, leukopenia

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12
Q

aplenic suscpeitble to

A

S. pneumoniae
Mengiococcal
H. influenza

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13
Q

hyperspenism

A

anemia
leukopenia
thrombocytopenia

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14
Q

non specific acute splenitis

A

blood borne infection

due to microbes themselves and cytokines

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15
Q

non specific acute splenitis morphology

A

200-400gm and soft
acute congested red pulp, may encroach and efface lymph follicles
neutrophils, plasma cells, and eos may be in white and red pulp
white pulp may undergo necorsis
rarely abscesses form

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16
Q

congestive splenomegaly

A

due to chornic venus outflow obstruction

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17
Q

systemic or central venous congestion

A
cardiac decompensation (right)
spleen rarely exceeds 500gm
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18
Q

cirrhosis of liver

A

main cause of massive congestive splenomegaly
schistosomiasis causes pipe-stem massive fibrosis
diffuse cirrhosis of alcoholics and pigment cirrhosis also cause profound enlargement

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19
Q

spontaneous portal v thrombosis

A

associated w/intrahepatic obstructive disease or inflammation of portal v after intraperitoneal infections

20
Q

morphology of congestive splenomegaly

A

long standing congestion produces marked enlargements
organ firm, capsule thickened fibrotic
red pulp fibrotic and cellular
elevated protal venous pressure stimulates collagen deposition in BM of sinusoids -> appear dilated
excessive destruction of RBCs

21
Q

CA associated w/splenomegaly

A
HL
NHL 
lymphocytic leukemias
MM
MPD
22
Q

Inflammatory conditions associated w/splenomegaly

23
Q

storage disease associated w/splenomegaly

A

gaucher disease
Niemann-picj
mucopolyaccharidoses

24
Q

splenic infacts

A

common lesions due to emboli usually from heart

25
bland infarcts
pale, wedge shaped, subcasular | overlying capsule covered w/fibrin
26
septic infarcts
supportive necorsis | large depressed scars when healed
27
neoplasm of spleen
rare except in meyloid and lymphoid tumors
28
benign tumors or spleen
``` fibrosma osteomas chondroma most common are lymphangioms and hemangiomas often cavernous ```
29
infections that increase risk of splenic rupture
mono malaria typhoid fever lymphoid neoplams
30
thymus cortical epithelium
polygonal | abundant cytoplasm w/dendritic extensions that contact adjacent cells
31
thymus medullary epithelium
densely packed often spindle shaped and scant cytoplasm | no interconnecting processes
32
hassel corpuscles
whorls of medullary epi with characteristic keratinzed cores
33
thymic hypoplasia
DiGeroge syndrome severe defects in T cell immunity other defects due to 22q11 deletion
34
isolated thymic cyts
uncommon lesions discovered incidentally lined by stratified or columnar epi serous or mucinous can be secondary to CA so if symptomatic should be investigated
35
thymic hyperplasia
appearance of B cell germinal centers w/in thymus more correctly termed thymic follicular hyperplasia
36
causes of thymic follicular hyperplasia
``` chronic inflammatory and immunological states Most frequently due to myasthenia gravis SLE scleroderma RA ```
37
thyomas
tumors of thymic epi
38
suptypes of thyomas
cytologically benign and noninvasice cytologically benign but invasive cytologcially malignant (thymic carcinoma)
39
thyoma stats
rare in kids M=F most in superior mediastinum sometimes occur in neck, thyroid, pulmonary hilus or elsewhere
40
thyomas morphology
lobulated, firm gray-white areas of cystic necrosis and calcification most encapsulated, but can rupture and infiltrate perithymic tissues and structures
41
non invasive thyomas
medullary type epi or mixture of medullary and cortical | spare inflitrate of thymocytes
42
invasive thyomas
coritcal epi w/abundant cyto and rounded vesicular nuclei numerous thermocytes sometimes cytological atypia ruptures thru capsule
43
thymic carcinoma
fleshy obviously invasive mets to lung squamous cell carcinomas are most common lymphoepithlioma-like carcinomas next most common
44
lymphoepithlioma-like carcinomas
sheets of cells w/indistinct borders close histological resembles to nasopharyngeal carcinoma 50% EBV
45
thyomas clinical
40% present with symptoms due to impingement on mediastinal structures 30-45% detected while evaluating myasthenia gravis
46
autoimmune conditions associated w/thyomas
``` MG hypogammaglobulinemia pure red cell aplasia graves disease pernicious anemia dermatomyositis-polymyositis cushings ```