Anatomical Pathology Flashcards

1
Q

What are the infective causes of Granulomatous lymphadenitis?

A

Mycobaterial infection
Toxoplamosis- Toxoplasma Gondii

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2
Q

What are the non-infective causes of Granulomatous lymphadenitis?

A

Sarcoidosis (schuamann bodies)
Crohn’s disease
reaction to tumour antigen
foreign body reaction - often occurs as a response to silicone compounds used in plastic surgery and joint replacement

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3
Q

What are the infective causes of necrotizing lymphadenitis?

A

Lymphogranuloma venereum- Chlamydial
Cat scratch disease- Bartonella henselae
Virus-herpes and CMV

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4
Q

What are the non-infective causes of necrotizing lymphadenitis?

A

Kikuchi’s disease
Systemic lupus erythematosus

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5
Q

What are the infective causes of Follicular hyperplasia?

A

Syphillis

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6
Q

What are the non-infective causes of Follicular hyperplasia?

A

Rheumatoid Arthritis

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7
Q

Describe the histological features of HIV-associated lymphadenopathy.

A

initially, follicles are hyperplastic and often markedly irregular in shape
Florid reactive hyperplasia (may be serrated, serpentine, or dumb-bell shaped)
containing macrophages and plasma cells
in some follicles, there is focal destruction of the dendritic reticulum cell meshwork which is associated with an invagination/implosion of mantle zone lymphocytes into germinal centers (‘follicular-lysis’)
imparts a moth-eaten appearance also called explosive follicular hyperplasia
later stages – eventual profound loss of germinal centre B-cells and depletion of paracortical T-cells
May have other opportunistic infections/malignancies present e.g. TB,CMV, Kaposi sarcoma, lymphoma

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8
Q

What are the risk factors associated with lymphomas?

A
  • Infection.
  • Cachexia.
  • Organ infiltration e.g. lungs.
  • Complications of treatment.
    • specifically related to therapeutic measures.
      – Corticosteroids and immunosuppressives
      – Endocrine dysfunction
      Second malignancies: acute myeloid leukemia, high-grade non-Hodgkin lymphomas, bone and soft tissue sarcomas, and breast cancer.
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9
Q

What are the risk factors associated with non-Hodgkins?

A

Viruses e.g. EBV, HTLV1, HHV8, HIV
Immunodeficiency
Primary – X-linked immunodeficiency
Secondary – AIDS, transplantation

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10
Q

Discuss the epidemiology of Burkitt’s Lymphoma.

A

Endemic - most common in Central Africa. Children 4-8 yrs. Presents with enlarged jaws, ovaries. Nodal enlargement not characteristic. Strong association with EBV infection.
Non-Endemic (Western) - intestinal involvement is most common (ileum) with mesenteric nodes. Older children,
AIDS associated

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11
Q

Describe how Hodgkins Lymphoma spreads.

A

Hodgkin lymphoma is a disease that spreads predominantly through lymphatics, and the tendency in most cases is for the tumour to spread to contiguous groups of lymph nodes.

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12
Q

Define Hypersplenism and list its treatment.

A

the term is applied to an association between peripheral blood pancytopenia and splenic enlargement
Splenectomy

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13
Q

Describe the morphology of congestive splenomegaly.

A

Cut Surface
beefy-red colour with inconspicuous white pulp
contains scattered firm brown nodules – Gamna Gandy bodies - represent areas of healed infarction - composed of fibrous and elastic tissue with abundant haemosiderin and dystrophic calcification

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14
Q

Describe how a systemic infection would affect the spleen.

A

may cause moderate splenomegaly
characterised by congestion and macrophage hyperplasia
white pulp- usually prominent

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15
Q

Describe how a bacterial infection would affect the spleen.

A

in response to infections e.g. bacterial endocarditis or localised abscesses
neutrophils can accumulate in the sinuses and medullary cords
if extreme – ‘acute septic splenitis’
becomes soft because of proteolytic enzyme action

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16
Q

Describe how a chronic malarial infection would affect the spleen.

A

may lead to massive splenomegaly
splenic capsule – thickened and fibrotic
cut surface – slate grey colour due to abundant malarial pigment

17
Q

Describe how a viral infection would affect the spleen.

A

especially infectious mononucleosis
may produce more severe splenomegaly
susceptible to rupture

18
Q

What are some storage disorders of the spleen?

A

Niemann Pick disease
Gaucher’s disease
Mucopolysaccharidoses

Marked red pulp expansion by macrophages whose cytoplasm is distended with the abnormal storage product

19
Q

Desribe the features of Hodgkins Lymphomas

A
20
Q

Describe the features of Hodgkin’s Lymphomas.

A

Non-classical
Nodular Lymphocyte predominant HL- Popcorn cell/ H and L
Classical:
Lymphocyte Rich: Reensteenberg Cells
Nodular Sclerosing: Lucunar variant RS cells
Mixed Cellularity: Mix number of granulocytes and lymphocytes, plus RS cells, and Mummified cells
Lymphocyte Depleted: Increase in RS cells.