Histopathology 13 - Histopathology of Systemic Disease Flashcards

(25 cards)

1
Q

What can JCV infection in HIV positive patients lead to?

A

Progressive multifocal leukoencephalopathy

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2
Q

What is the most common opportunistic infection in HIV positive patients?

A

CMV - affects retina and GIT

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3
Q

Recall causes of menigitis/encephalitis in HIV

A

meningitis - cryptococcus

encephalitis - toxoplasma gondii

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4
Q

Which cancers does HIV predispose you to?

A

Kaposi’s sarcoma

lymphoma - B cell, EBV

SSC, anus and cervix, HPV

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5
Q

Which herpes virus causes kaposi sarcoma?

A

HHV8

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6
Q

what is the defining histological feature of Mycobacteria?

A

Caseating granulomas (necrotic centre)– immunocompetent people

stains w/ acid fast bacilli

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7
Q

Cavitating TB – where is the predilection?

A

lung apices

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8
Q

What is the main histological finding in sarcoidosis?

A

Non-caseating granulomas

collection of macrophages with cuff of lymphocytes around

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9
Q

How does end-stage sarcoidosis appear on CXR?

A

‘Honeycomb’ lung

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10
Q

define IgG4 related disease

A

Inflammation by IgG4-AB producing plasma cells (polyclonal)

Fibrosis and obliteration of veins

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11
Q

Describe the histological features of IgG4 related disease

A

plasma rich cells, inflammatory infiltrate

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12
Q

What colour does IgG4 stain when positive?

A

Brown

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13
Q

Recall 3 diseases caused by IgG4 inflammation

A

Salivary and lacrimal glands: Mikulicz syndrome

Thyroid: Riedel thyroiditis

Peritoneum: Retroperitoneal fibrosis

Liver: Biliary obstruction

Pancreas: Autoimmune pancreatitis

Mass lesions: Inflammatory pseudotumour

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14
Q

Recall the histolpathological features associated with alcohol

A

Liver

fatty change (steatosis), steatohepatitis (neutrophils, mallory denk), cirrhosis, liver cell cancer (hepatocellular carcinoma)

GI Tract

acute gastritis, oesophageal varices

Nervous system

peripheral neuropathy, Wernicke-Korsakoff syndrome etc.

Cardiovascular system

dilated cardiomyopathy, hypertension, atheroma (and decreases it)

Pancreas

acute pancreatitis, chronic pancreatitis

Cancer

oral cavity, pharynx. oesophagus, liver and breast

Fetal alcohol syndrome

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15
Q

What is the structure of amyloid?

A

Beta pleated sheet that forms non-branching fibrils

Always contains P-component

resistant to enzymatic degradation

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16
Q

AA vs AL amyloidosis

A

AA

derived from serum amyloid A

e.g. RhA, Crohn’s Disease / chronic inflammatory diseases

AL

derived from light chains

e.g. multiple myeloma, B cell lymphoma

17
Q

What is the cause of AA amyloidosis?

A

Chronic inflammation

18
Q

Which conditions are particularly implicated in the development of AA amyloidosis?

A

Crohn’s
Rheumatoid arthritis

19
Q

What conditions can cause AL amyloidosis?

A

Myeloma
B cell neoplasms

20
Q

What is the link between transthyretin and amyloidosis?

A

Transthyretin mutation can –> cardiac amyloid

21
Q

What proteins are implicated in the second classification of amyloidosis?

A

Transthyretin (e.g. mutation)

Beta2-macroglobulin

peritoneal dialysis

Abeta2 protein

Alzheimer’s

Insulin, calcitonin

endocrine tumours

22
Q

What stain can be used for amyloid?

A

Congo red - gives green birefringence under polarised light

23
Q

Recall the features of cystic fibrosis

A

Pancreas

duct obstruction, exocrine atrophy

Salivary glands

duct obstruction, atrophy

Intestine

meconium ileus

Liver

biliary obstruction, cirrhosis

Lung

bronchial obstruction, superimposed infection with abscess formation (Staphylococcus aureus, Haemophilus influenzae and Pseudomonas aeruginosa)

Male genital tract

infertility, absence of the vas

24
Q

Histological features of amyloidosis

25
recall the clinical features of amyloidosis
Proteinuria, renal failure Restrictive cardiomyopathy, arrhythmias Autonomic neuropathy Carpal tunnel syndrome Macroglossia Bleeding on injury Also deposited in blood vessels, endocrine organs, liver, spleen