Infectious Disease 02: continued Flashcards

1
Q

What is a C/F of infection by S. mansoni and S. japonicum in the liver?

A

“pipestem fibrosis” leading to esophageal varices

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2
Q

What are the common manifestations of infection by S. Manson infection in the lungs?

A

angiomatoid lesions similar to those of idiopathic pulmonary hypertension

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3
Q

S. haematobium infection can cause squamous metaplasia in a certain part of the body leading to what condition?

A

squamous cell carcinoma of the urinary bladder

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4
Q

How is Lymphatic filariasis spread?

A

transmitted by mosquitoes and caused by closely related nematodes Wuchereria bacrofti and Braga speacials

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5
Q

What is a major C/F of lymphatic filariasis?

A

elephantiasis

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6
Q

What is required in development and reproduction of lymphatic filariasis?

A

Symbiotic Wolbachia bacteria infect filarial nematodes and are required for nematode development and reproduction

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7
Q

What are some other C/F of lymphatic filiariasis besides elephantiasis?

A

lymphedema of the extremities, scrotum, penis, or vulva

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8
Q

What are Meyers-Kouwenaar bodies?

A

Lung involvement by microfilariae is marked by eosinophilia caused by TH2 responses and cytokine production (tropical eosinophilia), dead microfilariae surrounded by stellate, hyaline, eosinophilic precipitates embedded in small epithelioid granulomas

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9
Q

Onchocerca volvulus is transmitted by what organisms? What is another name for infection by this organisms?

A

black flies, vector’s preferred habitat is near fast moving water hence higher incidence of disease near rivers “river blinds”

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10
Q

What is an onchocercoma?

A

ibrous capsule surrounding adult worms and a mixed chronic infiltrate that includes fibrin, neutrophils, eosinophils, lymphocytes, and giant cells

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11
Q

C/F of onchocerciasis?

A

Progressive eye lesions : punctate keratitis, sclerosing keratitis, sometimes accentuated by treatment with anti- filarial drugs (Mazzotti reaction)

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12
Q

C/F of prion diseases?

A

scrapie in sheep/goats, bovine fponigorm encephalopathy in cattle “mad cow” disease

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13
Q

Pathogenesis of prion disease.

A

Change in PrP from native PrPc form to an abnormal form PrPsc (scrapie_ or PrPres(protease resistant), PrPsc can imitate transformation of other PrPc

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14
Q

C/F of CJD?

A

Creutzfeldt-Jakob disease

rapidly progressive dementia

  • Periodic sharp and slow wave complexes in the EEG
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15
Q

Transmission of CJD?

A

deep implantation electrodes, contaminated human GH

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16
Q

Characteristic of those with CJD upon microscopy?

A
  • Spongiform transformation of cerebral cortex and deep gray matter structures (caudate, putamen)
  • No inflammatory infiltrate
17
Q

Immunochistochemistry of those with CJD?

A

proteinase K-resistant PrPsc in tissue

18
Q

Diagnostic tools to ID CJD?

A

western blot