Mycoses Flashcards

1
Q

SUPERFICIAL
MYCOSES

A

localized along hair shafts and in superficial epidermal cells

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2
Q

PITYRIASIS VERSICOLOR

A

a.k.a. tinea versicolor
chronic superficial infection of the stratum corneum
CA: Malassezia globosa, Malassezia furfur, Malassezia
sympodialis (dimorphic fungi)
◦ part of normal skin flora
◦ may also cause dandruff (seborrheic dermatitis)
◦ former genus: Pityrosporum
CF: discrete, serpentine, hyper-, or hypopigmented
maculae that develop on the skin, usually on the
chest, upper back, arms, or abdomen

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3
Q

PITYRIASIS VERSICOLOR
Diagnosis:
Treatment:

A

◦ KOH mount: “spaghetti and meatballs” (short
unbranched, nonpigmented hyphae and round
spores)
◦ Wood lamp: yellowish-white or copper-orange

◦ selenium sulfide
◦ topical/oral azole

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4
Q

TINEA NIGRA

A

a.k.a. tinea nigra palmaris
chronic and asymptomatic infection of the
stratum corneum
CA: Hortaea (Exophiala) werneckii
◦ a dematiaceous fungi
CF: dark (brown to black) discoloration,
often on the palm
Treatment: keratolytic solutions, salicylic
acid, azole antifungals

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5
Q

BLACK PIEDRA

A

CA: Piedraia hortae
◦ a dematiaceous fungi
CF: nodular infection of the
hair shaft
Treatment: removal of the
infected hair, application of
a topical antifungal agent

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6
Q

WHITE PIEDRA

A

CA: Trichosporon sp.
CF: larger, softer,
yellowish nodules on the
hair shaft
Treatment: removal of the
infected hair, application of
a topical antifungal agen

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7
Q

CUTANEOUS
MYCOSES

A

keratinized tissues such as skin, hair, and nails
Transmission: direct contact

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8
Q

DERMATOPHYTOSIS

A

was mistaken for ringworm or tinea
CA: dermatophytes such as Microsporum,
Trichophyton, Epidermophyton sp.
◦ Geophilic – soil, acute infections
◦ Zoophilic – animals, acute infections
◦ Anthropophilic – humans, chronic infections
CF: raised circular lesions
◦ restricted to nonviable skin because most are unable
to grow at 37°C or in the presence of serum

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9
Q

DERMATOPHYTOSIS LOCATION

A

Tinea capitis Scalp hair
Tinea barbae Beard
Tinea faciei Face
Tinea manuum Hands
Tinea unguium (onychomycosis) Nails
Tinea corporis Trunk
Tinea imbricata Trunk and Limbs in concentric/annular pattern
Tinea cruris (jock itch) Groin
Tinea pedis (athlete’s foot) Feet

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10
Q

DERMATOPHYTOSIS
Diagnosis:
Treatment:

A

◦ KOH mount: hyaline, septate, branching hyphae; chains of arthroconidia
(diagnostic)

◦ removal of infected and dead epithelial structures
◦ topical antifungal
◦ keeping areas dry
◦ avoiding sources of infection (infected pet or shared bathing facilities)

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11
Q

CANDIDIASIS OF SKIN, MUCOSA, OR
NAILS

A

a.ka. moniliasis
occurs in broad-spectrum antibiotic overuse
Risk factors: AIDS, pregnancy, diabetes, young or old age, birth control pills, trauma
(burns, maceration of the skin
Pathogenesis: increase in the local census of Candida and damage to the skin or
epithelium that permits local invasion by the yeasts and pseudohyphae
CA: Candida albicans
Diagnostics:
◦ KOH mount: yeast and/or pseudohyphae

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12
Q

Thrush

A

◦ white, adherent, painless, discrete or confluent patches
of whitish pseudomembranes on the tongue, lips,
gums, palate, esophagus
◦ can form an intractable biofilm
◦ should prompt investigation of underlying HIV
infection

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13
Q

Vulvovaginitis

A

◦ irritation, pruritus, & vaginal discharge (usually thin but
may contain whitish “curds” if severe)
◦ not usually associated w/ HIV infection

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14
Q

Paronychia

A

◦ painful swelling at the nail–skin interface

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15
Q

Onychomycosis

A

◦ painful, erythematous swelling of the nail fold that may
destroy the nail

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16
Q

Intertrigo

A

◦ erythematous irritation w/ redness & pustules in skin
folds

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17
Q

Balanitis

A

◦ erythematous-pustular infection of the glans penis

18
Q

Erosio interdigitalis blastomycetica

A

◦ infection between the digits of the hands or toes

19
Q

Diaper Rash

A

◦ common erythematous, pustular perineal infection in
infants

20
Q

CANDIDIASIS OF SKIN, MUCOSA, OR
NAILS
Treatment:

A

◦ topical nystatin
◦ oral ketoconazole or fluconazole

21
Q

CHRONIC MUCOCUTANEOUS
CANDIDIASIS (CMC)

A

formation of granulomatous candidal lesions on any or all cutaneous (hair, nails, skin)
and/or mucosal surfaces
persists despite intermittent antifungal therapy
associated with:
◦ immunologic dysfunction – failure of Th17 lymphocytes to secrete type-17 cytokines in response
to Candida antigens
◦ autoimmunity
◦ hypoparathyroidism
usually comes in infancy or within the first two decades of life
CF:
◦ chronic, raised, and crusty highly disfiguring keratitic lesions on the skin, oral mucosa, and scalp
◦ exophytic outgrowths on the skin

22
Q

SUBCUTANEOUS
MYCOSES

A

tissues beneath the skin
Transmission: direct implantation of spores or mycelial fragments into a
puncture wound in the skin
fungi normal reside in soil or vegetation

23
Q

SPOROTRICHOSIS

A

a.k.a. rose gardener’s disease
chronic granulomatous infection typically followed by 2° spread
with involvement of the draining lymphatics and lymph nodes
caused by trauma associated with plants
CA: Sporothrix schenckii (dimorphic fungi)
CF:
◦ Lymphocutaneous – granulomatous nodule that may
progress to a necrotic or ulcerative lesion; draining lymphatics
become thickened and cord-like
◦ Primary pulmonary sporotrichosis – mimics chronic cavitary
tuberculosis when inhaled by those with impaired cellular
immunity

24
Q

SPOROTRICHOSIS
Diagnosis:
Treatment:

A

◦ Histologic examination: cigar-shaped yeast,
often with surrounding asteroid body

◦ KISS
◦ oral or systemic antifungal

25
Q

CHROMOBLASTOMYCOSIS

A

a.k.a. chromomycosis
subcutaneous mycotic infection caused by traumatic
inoculation of fungi, which reside in soil and vegetation
CA: Phialophora verrucosa, Fonsecaea pedrosoi,
Fonsecaea compacta, Rhinocladiella aquaspersa,
Cladophialophora carrionii
◦ dematiaceous fungi
Diagnosis:
◦ KOH mount: sclerotic bodies (pathognomonic; dark brown,
thick-walled, septate fungal forms that resemble large
yeasts)

CF:
◦ slow development of progressive granulomatous lesions that
induce hyperplasia of the epidermal tissue
◦ verrucous and wart-like with extension along the draining
lymphatics
◦ cauliflower-like nodules with crusting abscesses
◦ small ulcerations or“black dots” of hemopurulent material
◦ rarely, elephantiasis
Treatment:
◦ surgical excision
◦ local heat
◦ oral or systemic antifungal

26
Q

PHAEOHYPHOMYCOSIS

A

presence of darkly pigmented
septate hyphae in tissue
CA: Exophiala jeanselmei,
Phialophora richardsiae,
Bipolaris spicifera, Wangiella
dermatitidis
CF:
◦ SC: solitary encapsulated cyst
◦ Systemic: sinusitis, brain
abscess (fatal)

27
Q

PHAEOHYPHOMYCOSIS
Diagnosis:
Treatment:

A

◦ Histologic examination: large hyphae w/
accompanying yeast cells; melanin in cell wall

◦ oral or systemic antifungal

28
Q

MYCETOMA

A

chronic subcutaneous infection induced by traumatic
inoculation with fungi (eumycetoma) or actinomycetous
bacteria (actinomycetoma, more severe)
CA: Pseudallescheria boydii, Madurella mycetomatis,
Madurella grisea, Exophial jeanselmei, Acremonium
falciforme
◦ dematiaceous molds
CF:
◦ local swelling of the infected tissue with suppuration,
abscesses, granulomata and interconnecting, often
draining, sinuses or fistulae containing granules
◦ may spread to muscle and bone

29
Q

MYCETOMA
Diagnosis:
Treatment:

A

◦ Histologic examination: granules (microcolonies of the agent embedded in
tissue material)

◦ surgical debridement or excision
◦ long-term topical, oral, or systemic antifungal

30
Q

PRIMARY SYSTEMIC
MYCOSES

A

many organs deep within the body
Transmission: inhalation

a.k.a. endemic mycoses
caused by dimorphic fungi

31
Q

COCCIDIOIDOMYCOSIS

A

a.k.a. San Joaquin Valley fever, desert rheumatism
CA: Coccidioides posadasii, Coccidioidesimmitis
CF:
◦ 60%: asymptomatic
◦ 40%: self-limited influenza-like illness with fever, malaise,
cough, arthralgia, and headache
◦ 15%: hypersensitivity reactions, e.g. rash, erythema
nodosum, erythema multiforme
◦ pulmonary infiltrates, pneumonia, pleural effusions, or
nodules
◦ <1%: secondary or disseminated coccidioidomycosis (CNS,
bone)

32
Q

COCCIDIOIDOMYCOSIS
Diagnosis:
Treatment:

A

◦ Histologic examination:
spherules (arthroconidia
that enlarge, become
rounded, and develop
internal septations, and
contain endospores)

◦ oral or systemic antifungal

33
Q

HISTOPLASMOSIS

A

a.k.a. spelunker’s disease (transmitted from
bird and bat guano)
the most prevalent pulmonary fungal
infection in humans and animals
CA: Histoplasma capsulatum
◦ facultative intracellular parasite
◦ able to replicate within alveolar macrophages
Diagnosis:
◦ Histologic examination: yeast with narrow-based
budding; intracellular yeasts
CF:
◦ Acute
◦ self-limited flulike syndrome with fever, chills, myalgias, headaches, and nonproductive cough
◦ CXR: hilar lymphadenopathy and pulmonary infiltrates or nodules (heal with calcification)
◦ Chronic
◦ reactivation
◦ progressive inflammation, tissue necrosis, and fibrosis mimicking cavitary tuberculosis
◦ precipitated by structural lung disease (e.g., emphysema)
◦ Progressive disseminated histoplasmosis (PDH) in immunosuppressed
Treatment:
◦ oral or systemic antifungal

34
Q

BLASTOMYCOSIS

A

a.k.a. North American blastomycosis,
Gilchrist disease
a chronic infection with granulomatous and
suppurative lesions that is initiated in the
lungs, but dissemination may occur to any
organ but preferentially to the skin and
bones
CA: Blastomyces dermatitidis
Diagnostic Test:
◦ Histologic examination: yeast with broad-based
budding
CF:
◦ Acute LRTI (fever, malaise, night sweats, cough, and myalgias)
◦ Chronic pneumonia – pyogranulomatous reaction with neutrophils and
noncaseating granulomas
◦ Disseminated blastomycosis (skin, bone, CNS, larynx, GUT)
Treatment: oral or systemic antifungal

35
Q

PARACOCCIDIOIDOMYCOSIS

A

a.k.a. SouthAmerican blastomycosis
CA: Paracoccidioides brasiliensis
Diagnostic Test:
◦ KOH mount: yeasts with budding in
steering-wheel pattern
CF:
◦ Acute/Juvenile Form:
◦ uncommon, usually <30 years old
◦ disseminated infection of the reticuloendothelial system
◦ Chronic/Adult Form:
◦ ~90%, usually in older men
◦ progressive pulmonary disease, in the lower lobes, with fibrosis
◦ ulcerative and nodular mucocutaneous lesions in mucous membranes of the upper respiratory
tract
Treatment:
◦ oral or systemic antifungal

36
Q

SYSTEMIC CANDIDIASIS

A

the most prevalent systemic mycosis
associated with corticosteroids or other immunosuppressive agents; with hematologic
diseases such as leukemia, lymphoma, and aplastic anemia; or with chronic
granulomatous disease
due to candidemia caused by indwelling catheters, surgery, IV drug abuse, aspiration,
or damage to the skin orGIT
CA: C. albicans, C. parapsilosis, C. glabrata, C. tropicalis, C. guilliermondii, C. dubliniensis
◦ an endogenous opportunist (normal flora of the skin, mucous membranes, andGIT)
◦ C. albicans – dimorphic unlike other species
may develop occult lesions anywhere, esp. the kidney, skin, eye, heart, and meninges
CF:
◦ Endocarditis
◦ Kidney infections
◦ Macronodular skin lesions
◦ Endophthalmitis
Treatment:
◦ oral and systemic antifungal

37
Q

CRYPTOCOCCOSIS

A

more common in patients with
HIV/AIDS
CA: Cryptococcus neoformans,
Cryptococcus gattii
◦ have polysaccharide capsule
◦ present in pigeon droppings
Diagnostic test:
◦ Microscopic examination: encapsulated
yeast w/ India ink
CF:
◦ pulmonary infection –
asymptomatic or influenza-like
respiratory infection
◦ osteomyelitis
◦ chronic meningitis (most common)
Treatment:
◦ combination systemic antifungals

38
Q

ASPERGILLOSIS

A

CA: Aspergillus fumigatus
DiagnosticTest:
◦ acute-angle septate hyphae, uniform
in width

Allergic Forms
• Allergic Bronchopulmonary Aspergillosis – asthma, recurrent chest
infiltrates, eosinophilia; both type I and type III skin test
hypersensitivity
• Extrinsic Allergic Alveolitis
Aspergilloma and Extrapulmonary Colonization
• Fungus Ball – cough, dyspnea, weight loss, fatigue, and hemoptysis
• increased risk in previous cavitary disease
• a late manifestation of chronic cavitary pulmonary aspergillosis
• infection of nasal sinuses, the ear canal, the cornea, or the nails
Invasive Aspergillosis
• associated with lymphocytic or myelogenous leukemia and
lymphoma, stem cell transplant recipients, individuals taking
corticosteroids, and AIDS
• fever, cough, dyspnea, and hemoptysis
• thrombosis, infarction, and necrosis due to presence in

TREATMENT
combination systemic antifungals
antiretroviral therapy in AIDS
Immune Reconstitution Inflammatory Syndrome (IRIS)
◦ occurs in 1/3 of ART-treatedAIDS patients
◦ a paradoxical worsening of preexisting, untreated, or partially treated opportunistic
infection

39
Q

MUCORMYCOSIS
(ZYGOMYCOSIS)

A

associated with acidotic patients (esp.
in DM), leukemias, lymphoma,
corticosteroid treatment, severe burns,
immunodeficiencies, dialysis with
deferoxamine
CA: Rhizopus oryzae (most common),
Rhizomucor, Lichtheimia,
Cunninghamella, Mucor sp.
Diagnostics:
◦ Histologic examination: ribbon-like aseptate
hyphae
CM:
◦ Rhinocerebral Mucormycosis (most common)
◦ invasion of the sinuses, eyes, and brain
◦ edema of the involved facial area, a bloody nasal exudate, and orbital cellulitis
◦ Thoracic Mucormycosis
Tx:
◦ surgical debridement
◦ systemic antifungal

40
Q

PNEUMOCYSTIS PNEUMONIA

A

CA: Pneumocystis jiroveci (carinii)
◦ formerly thought of as a protozoan
◦ 2 forms: trophozoite and cyst
associated with AIDS
CF:
◦ Acute or Subacute Pneumonia
◦ initially characterized by a vague sense of dyspnea alone that subsequently manifests as fever and nonproductive cough with
progressive SOB
◦ may progress to respiratory failure and death
◦ Extrapulmonary Manifestations
◦ rare
◦ can include involvement of almost any organ, most notably the lymph nodes, spleen, and liver
Treatment:
◦ cotrimoxazole
◦ ART in AIDS

41
Q

TALAROMYCOSIS (PENICILLIOSIS)

A

associated w/ HIV/AIDS, tuberculosis,
corticosteroid treatment,
lymphoproliferative diseases
CA: Talaromyces (Penicillium)
marneffei (dimorphic fungi)
Diagnostic Test:
◦ Histologic exam: oval or elliptical yeast-
like organisms with transverse central
septation

CF:
◦ fungemia, skin lesions, and systemic
involvement of multiple organs, esp. the
RES
◦ mimic disseminated histoplasmosis
◦ cough, fever, fatigue, weight loss, and
lymphadenopathy; cutaneous or
subcutaneous papules, pustules, or rashes
◦ mortality rate >90% if untreated
Treatment:
◦ systemic antifungal