Systemic Pathology Flashcards

1
Q

What are the complications of HIV?

A
  • Opportunistic Infections
  • Tumours
  • Central nervous system diseases
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2
Q

How does symptoms change with CD4 and RNA over time?

A
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3
Q

What are the HIV opportunistic infections?

A

Pneumocystis jiroveci: pneumonia
• CMV: especially retina and GIT
• Candida
• Tuberculosis and atypical mycobacteria
• Cryptococcus: meningitis
• Toxoplasma gondii: encephalitis and mass lesions
• JC papovavirus: progressive multifocal leukoencepalopathy
• Herpes simplex
• Cryptosporidium, Isospora belli, microsporidia: GIT

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4
Q

What is this showing?

A

Endoscopy:
Oesophageal ulcer
CMV

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5
Q

What is this?

A

(a) CMV nuclear inclusion
(b) Immunohistochemistry
for CMV

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6
Q

What are the HIV associated tumours?

A

• Kaposi’s sarcoma:
HHV-8

• Lymphoma:
systemic, CNS or body cavity based
B cell lymphomas
EBV

• Others:
Squamous cell carcinoma
Anus and cervix
HPV

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7
Q

How does a Kaposi sarcoma look Histologically?

A

A. The dermis is expanded by a solid
tumour.
B. Fascicles of relatively monomorphic
spindled cells, with slit-like vascular
channels containing erythrocytes.
C. The nuclei of the tumour cells
demonstrate immunoreactivity for
HHV-8.

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8
Q

What CNS diseases does HIV cause?

A
  • Progressive encephalopathy = AIDS dementia complex
  • Plus opportunistic infections and tumours
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9
Q

What does CNS HIV lymphoma look like?

A
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10
Q

What is the pathology of mTB?

A
  • Caseating granulomas
  • Demonstration of acid fast bacilli
  • Cavitating lesions
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11
Q

What kind of granuloma is this?

A

Caseous

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12
Q

Where can TB infect?

A

• Lung
• Lymph node
• Bone: e.g. vertebra- potts
• Heart: e.g. pericarditis
• GIT: e.g. peritonitis
• CNS: e.g. meningitis
etc.

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13
Q

What are the extrapulmonary features of mTB?

A
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14
Q

What is the pathology of sarcoidosis?

A
  • Non-caseating granulomas
  • A diagnosis of exclusion.
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15
Q

What is this?

A

Sarcoidosis

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16
Q

Where can sarcoid effect?

A
  • Lung: scattered granulomas, heal with fibrosis
  • Lymph nodes: usually hilar and mediastinal
  • Spleen
  • Liver
  • Heart
  • Joints
  • Bone marrow
  • Skin: nodules, plaques or macules
  • Eyes: iritis, choroid retinitis, lacrimal glands
  • CNS
  • Salivary glands
17
Q

What is IgG4 related disease?

A
  • Inflammation dominated by IgG4 antibody producing plasma cells
  • Fibrosis, obliteration of veins
18
Q

What is this?

A

IgG4

19
Q

Where does IgG4 related disease effect?

A
  • Salivary and lacrimal glands: Mikulicz syndrome
  • Thyroid: Riedel thyroiditis
  • Peritoneum: Retroperitoneal fibrosis
  • Liver: Biliary obstruction
  • Pancreas: Autoimmune pancreatitis
  • Mass lesions: Inflammatory pseudotumour
20
Q

What can alcohol cause?

A

• Liver: fatty change (steatosis) , fatty liver hepatitis (steatohepatitis),
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
• Fetal alcohol syndrome
• Cancer: oral cavity, pharynx. oesophagus, liver and breast

21
Q

What are the stages of ALD?

A

Normal
Steatosis
Steatohepatitis
Fibrosis
Cirrhosis
HCC

22
Q

10

A

10

23
Q

Where does CF present?

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

What is amyloid?

A

Deposition of an abnormal proteinaceous substance in non branching
fibrils, 7.5-10nm diameter
• Always contains P component
• Beta-pleated sheet structure
• A variety of proteins can take on this conformation
• Resistant to enzymic degradation

25
Q

What is amyloid classification?

A

•AA - derived from serum amyloid A
e.g. Crohn’s Disease, Rheumatoid
arthritis
•AL - derived from light chains
e.g. multiple myeloma, B Cell
lymphoma

26
Q

What types of amyloid causes certain diseases?

A
  • Transthyretin e.g. mutation
  • Beta2-macroglobulin – peritoneal dialysis
  • Abeta2 protein - Alzheimer’s
  • Insulin, calcitonin – endocrine tumours
27
Q

What is the staining for amyloid?

A

Stains with Congo Red dye
This shows apple green birefringence under polarised light

28
Q

What are the clinical features of amyloidosis?

A

• Proteinuria, renal failure
• Restrictive cardiomyopathy, arrhythmias
• Autonomic neuropathy
• Carpal tunnel syndrome
• Macroglossia
• Bleeding on injury
• Also deposited in blood vessels, endocrine organs,
liver, spleen

29
Q

What are the causes of granulomas in the liver?

A

Sarcoidosis

TB

Drug induced

Schistosomiasis

Malignancy

30
Q

What are the different types of liver damage due to alcohol?

A

Steatosis

Steatohepatitis

Fibrosis

Cirrhosis

31
Q

What type of amyloid is associated with multiple myeloma?

A

AL amyloid derived from light chain