ENT Fungal Infections Flashcards

1
Q

Describe the etiology/RF of candidiasis

A

candida albicans, opportunistic, found in mouth, vagina, feces

RF immunosuppression, hormonal fluctuation, augmentin

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2
Q

Describe the etiology of mucous candidiasis

A
  • oral (thrush)
  • angular cheilitis
  • esophagitis (AIDS defining disease)
  • vaginitis
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3
Q

Describe the etiology/RF for invasive candidiasis

A

Candida in the bloodstream

Risk factors
- immunocompromised
- infection
- broad spectrum abx use
- recent chemo (neutropenia)
- recent surgery/ICU stay

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4
Q

Describe the clinical presentation of candida esophagitis

A
  • substernal odynophagia
  • gastroesophageal reflux
  • nausea
  • fever
  • oral involvement
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5
Q

Describe the clinical presentation of invasive candidiasis

A

several days of fever unresponsive to board spectrum abx, hx risk factors,
- organ dysfunction, malaise, fever, tachy, hypotension, AMS, hepatosplenomegaly, maculopapular/nodular rash, resembles bacterial sepsis

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6
Q

Describe the diagnostic testing for candidiasis

A

KOH (wet prep) or fungal culture

Candida esophagitis: endoscopy w/ biopsy & culture

Invasive candidiasis: blood cultures positive only 50% of the time

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7
Q

Describe the treatment for oral candidiasis

A

Mild: clotrimazole troche, nystatin suspension

Mod-Severe: Fluconazole

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8
Q

Describe the treatment for vaginal candidiasis

A

miconazole 2% cream, Clotrimazole 1-2% cream, Terconazole cream/suppository, Fluconazole PO

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9
Q

Describe the treatment for candida esophagitis

A

Fluconazole PO, Itraconazole PO tablet/solution

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10
Q

Describe the treatment for invasive candidiasis

A

refer to ID for echinocandins

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11
Q

What is the most common opportunistic infection in HIV

A

oral candidiasis

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12
Q

Describe the etiology/RF of cryptococcosis

A

Cryptococcus neoformans (pigeon poop, soil)

Transmitted through contaminated vegetation, inhalation of spores, dissemination from lungs

RF immunosuppressed, disease burden in South Asia & Africa

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13
Q

Describe the clinical presentation of cryptococcosis

A

Painless skin nodules mimicking molluscum contagiosum, cutaneous erythematous papules, vesicles, macules, ulcers

Skeletal involvement, infection can harbor in heart, bone, liver, kidney, adrenals, eyes, prostate, lymph nodes

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14
Q

Describe the clinical presentation of cryptococcal meningitis

A

insidious onset, headache (1st sx), progressive confusion, AMS, fever, seizure, stiff neck, photophobia

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15
Q

Describe the clinical presentation of pulmonary cryptococcosis

A

may be asymptomatic, simple nodules, cough, dyspnea, hemoptysis, fever, respiratory issues

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16
Q

Describe the diagnostic testing for cryptococcosis

A

LP for suspected meningitis
- CSF gram stain: budding, encapsulated yeast
- CSF crypto antigen
- CSF culture
- india ink prep

Serum crypto antigen: usually positive in pts with AIDS

Chest x-ray may appear with diffuse interstitial pneumonia

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17
Q

Describe the treatment for cryptococcosis

A

Consult ID

IV amphotericin B x14 days then 8 weeks fluconazole PO, +/- flucytosine (toxic, $$$)

Avoid steroids

18
Q

Describe the etiology/RF of histoplasmosis

A

Histoplasma Capsulatum (mold in environment, yeast at body temp)

Soil contaminated with bird/bat droppings & spores carried by air & inhaled

Spores active for 10 years

RF: farmers, endemic areas, Ohio river valley, spelunking, immunosuppression

19
Q

Describe the clinical presentation of histoplasmosis

A

Vary d/t extent of exposure, immune response, underlying lung disease

Most cases asymptomatic or mild, pneumonia: fever, cough, mild central chest pain

20
Q

Describe the clinical presentation of acute pulmonary histoplasmosis

A

mild flu-like to severe pneumonia, long term (progressive disseminated histo in HIV - multiple organ involvement, fulminant, rapidly fatal)

21
Q

Describe the diagnostic testing for histoplasmosis

A

Pulm: sputum culture rarely positive, histoplasmosis antigen in urine & serum

Disseminated: pancytopenia, blood/bone marrow culture positive 80%, histo antigen in urine 90% sensitive

Chronic: anemia

Chest x-ray with hilar LAD

22
Q

Describe the treatment for histoplasmosis

A

Oral itraconazole BID weeks to months depending on severity

IV amphotericin B for severe illness with CNS involvement

AIDS-related histo: lifelong suppressive therapy with itraconazole PO qd

23
Q

Describe the complications of pulmonary histoplasmosis

A

granulomatous mediastinitis

24
Q

Describe the etiology of pneumocystosis

A

Pneumocystis jirovecii (worldwide distribution w/ airborne transmission)

Opportunistic: occurs in 80% of pts with AIDS who are not receiving prophylaxis

Most kids exposed by age 4 (asymptomatic - latent)

25
Describe the clinical presentation of pneumocystosis in pts with HIV
subacute onset over weeks, pneumonia sxs with progressively worsening dyspnea, tachypnea, cough, fever, chills, weakness, fatigue
26
Describe the clinical presentation of pneumocystosis in pts without HIV
more acute onset & fulminant resp failure, abrupt tachypnea, dyspnea, fever, cough
27
Describe the diagnostic testing for pneumocystosis
CXR: normal or diffuse interstitial infiltrates Cannot be cultured Can diagnose via stains or PCR on resp specimens
28
Describe the treatment for pneumocystosis
PO TMP-SMX (Bactrim) QID-QID Add prednisone for moderate to severe disease
29
Describe the prognosis for pneumocystosis
100% fatality in immunodeficient pts if tx is not early 30% recurrence in pts with AIDS who don’t receive prophylaxis
30
Describe the etiology of blastomycosis
Blastomyces dermatitidis Inhaling spores through outdoor activities, occupational exposure Affects immunocompetent individuals most commonly as a chronic pulmonary infection Dissemination: skin, bones, urogenital system
31
Describe the clinical presentation of blastomycosis
Cough, fever, dyspnea, chest pain, purulent cough, weight loss, extreme exhaustion, ARDS
32
Describe the diagnostic testing for blastomycosis
grows on culture
33
Describe the treatment for blastomycosis
Itraconazole PO 6-12 mos IV amphotericin B for severe disease, CNS involvement, or tx failure
34
Describe the etiology of coccidioidomycosis
2 species of coccidioides Inhalation of spores from dry soil (SW US, central america, south america) Aka Valley Fever
35
Describe the clinical presentation of coccidioidomycosis
Erythema nodosum, flu like symptoms (malaise, fever, arthralgia, HA, cough) Can disseminate to CNS, bones, skin
36
Describe the diagnostic testing for coccidioidomycosis
CXR findings vary Serologic testing
37
Describe the treatment for coccidioidomycosis
Itraconazole QD-BID 6mos+ IV amphotericin B or fluconazole for severe/meningitis
38
Describe the complications of coccidioidomycosis
high mortality if it disseminates (especially to the CNS)
39
Describe the structure of fungi
- polysaccharide coating (india ink stain test) - cell wall with carbs & proteins - 2 layer membranes (ergesterol in fungi, cholesterol in human cells) - target for meds
40
Describe some common superficial fungal infections
affect only the top layer of skin - tinea/pityriasis versicolor - typically diagnosed with KOH - typically treated with topicals
41
Describe some cutaneous fungal infections
- can be 30+ species - fungi secrete keratinase (scaling, brittling, loss of hair) - tinea corporis, cruris, pedis, capitis, unguium - diagnosed with KOH or culture - treated with -azoles, griseofluvin, terbinafine