Toxoplasmosis, MAC, Fungal Diseases Flashcards

1
Q

What causes toxoplasmosis

A

protoxoa: toxoplasma gondii

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2
Q

animal that T. gondii completes its reproductive cycle

A

cat

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3
Q

where does toxoplasma live, when is it not dormant

A

nucleated cells, when immunosuppressed

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4
Q

4 ways of infection by toxoplasmosis

A

contaminated meat, produce, water; ingestion cat feces/soil, vertically (mother-fetus), organ transplant

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5
Q

How many in US are seropositive for T. gondii

A

11% age 6-49

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6
Q

most common mode of transmission in us of toxoplasmosis

A

consumption undercooked meat

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7
Q

climate preferred by toxoplasmsois

A

hot humid (SW USA)

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8
Q

what is third most common cause of lethal foodborne disease in US

A

toxoplasmosis

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9
Q

S/S toxoplamsosi (4)

A

fevers/chills/sweats, cervical lymphadenopathy, myalgia/arthralgia/HA/sore throat/rash, chorioetinitis (inflam eye)

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10
Q

diagnosis of toxoplasmosis

A

serologic testing with toxoplasmosis IgM antibody levels

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11
Q

treatment of toxoplasmosis

A

3 drug regimen: pyrimethamine, sulfasalazine, leucovorin calcium
competent pts = 2-4wks, immunocompromised = longer

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12
Q

Congenital toxoplasmosis risk vs severity

A

1st trimester 15% low risk, disease most severe

3rd trimester 60% high risk, disease sublcinial/symp not at birth

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13
Q

Do congenital toxoplasmosis children present at birth

A

2/3 DON’T

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14
Q

classic traid of congenital toxoplasmosis

A

retinochorionitis, intracranial calcifications, hydrocephalus (tirad rarely seen)

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15
Q

50% of immunocompromisd pts get what with toxoplasmosis

A

CNS involvement: sz, blance changes, cranial nerve deficits, focal deficits, AMS, HA

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16
Q

T/F immunocompromised pts will get flulike symp and lymphadenopathy like comp pts

17
Q

MRI with contrast might show wat in immunocmprised pts with toxopalsmosis

A

encephalitis, mass lesions or meningoencephalitis

18
Q

how does histoplasmosis infect

A

inhalation of fungal spores (bird droppings, contaminated soil aersolizes during construction)

19
Q

pathophys of hisoplasmosis

A

pulmonary macrophages ingest it but can’t kill it, fungus grows and divides inside, macrophage takes it through blood to lungs, spleen, liver, fungus trapped in fibrotic, calcified caseating granuoloma

20
Q

What type of hypersensitivity reaction occurs with histoplasmosis

A

delayed-type hypersensitity rxn (t-lymph develops immunity for macrophages and lymphocytes to sterilize granulomas)

21
Q

how common is asymptomatic histoplasmosis

A

90% of competent w/ low exposure are asymp; others flu-like for 1-4 wks

22
Q

If pt has calcifications on incidental CXR what might they have

A

might have had asymptomatic histoplasmosis years ago

23
Q

acute/subsactute pum histopalsmosis S/S, who gets it, recovery prognosis

A

fever, myalgia, abd pain, rales, heavy exposure competent or less in immunocompromised; ill wks-months; almost never fatal

24
Q

chronic pulmonary histoplasmosis; S/S; who gets it

A

older pts with COPD, progressive apical cavitary lesions, weight loss, productive cogh, fever, lasts 3+ months, (possible TB b/c apical)

25
Progressive disseminated histoplasmosis
immunocomprimsed (like pts on TNF inhibitors), develop fever, cough, dyspnea, 20% AMS, pericardial effusions, ulcerative lesions of mucous memb and viscera; fatal w/in weeks
26
3 main and 3 other S/S that indicate histoplasmosis
pneumonia with lymphadenopathy, cavitary lung disease, pulm manifestations w/ arthritis or arthragai plus erythema nodosum minor: mediastinal or hilar masses, pericarditis w/ mediastinal lymphadenopathy, suspected sacroidosis
27
systemic manifestations with pts with disseminated histoplasmossi
pancytopenia, LFT abn, erythema nodosum
28
how to diagnose histoplasmosis
blood cutlures, complement fixation antibody titer, serum or urine antigen detection assay (none close to 100% sensitive) CT or MRI to see extenet of disease
29
2 invasive procedures and 2 meds for histoplasmosis
bronchoscopy, pericardial window | itraconazole for wks up to a year; if severe: amphotericin B used briefly