CPC Feb 2 2009 Dr Ruenger

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    In the name of ALLAH, the Beneficent the Merciful

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    CPC

    with

    Thomas Ruenger MD Phd

    Muhammad Khawar Nazir

    BUMC Dermatology2nd Feb. 2009

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    History

    15 years old boy,

    PC: Brown big itchy and painful bumps on facesince last 1 year

    h/o trauma with lead pencil on left hand

    1 month after trauma, lesions started at facewhich are spreading

    No family h/o skin diseases h/o home made topical remedies

    No past medical history

    Review of systems : Insignificant

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    Examination

    Face, almost whole central face sparing eyesand chin

    Hyperpigmented verrucous induratedplaques, firm, well defined, mild erythema,few erosions, few areas of pus on cheeks and

    nose

    Peripheral borders are elevated, centralscarring

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    Differenital Diagnosis

    Cutaneous tuberculosis

    Deep Fungal Infection

    Leishmaniasis

    Atypical Mycobacterial Infection

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    Diagnosis

    All tests were normal

    Skin Biopsy

    CHROMOBLASTOMYCOSIS

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    TREATMENT

    Terbinafin

    Fluoconazol

    Cryotherapy

    Psychological help

    Plastic Surgery

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    CHROMOBLASTOMYCOSIS

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    Synonyms

    Chromomycosis

    Cladosporiosis

    Verrucous dermatitis

    Phaeosporotrichosis

    Pedroso's disease

    Fonseca's disease

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    INTRODUCTION

    verrucous dermatosis caused by several

    genera of dematiaceous, or pigmented, fungi

    Typically chronic in nature, an expandingverrucous plaque on the lower, or occasionally

    upper, extremity is the classic presentation

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    INTRODUCTION

    6 fungi are responsible for the vast majority of cases:

    Fonsecaea pedrosoi,

    Phialophora verrucosa,

    Cladosporium carrionii, Fonsecaea compacta,

    Fonsecaea monophora and

    Rhinocladiella aquaspera.

    The clinical presentation and colonial morphologies of each ofthese fungi are very similar, and differentiation is based onmicroscopic and conidial characteristics

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    HISTORY

    Pedroso first recognized chromoblastomycosis

    in 1911

    Four years later, Medlar & Lane reported the

    first case in the US (in Boston)

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    Confusionoverthe propernaming

    At one point, chromoblastomycosis was thoughtto be closely related to blastomycosis; however,

    cellular division does not occur via budding(blasto-) but rather via internal septation, hencethe preference for the term chromomycosis

    Nonetheless, some authors have argued thatchromomycosis is also confusing, because it hasthe same meaning as phaeohyphomycosis, andso they prefer the term chromoblastomycosis

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    EPIDEMIOLOGY

    Most commonly found in tropical and subtropical climates

    Occasionally in temperate zones such as the US, Europeand Canada

    Farmers, miners and others working in rural areas are athigher risk than the general population

    Men 20 to 60 years of age are more often affected,probably due to their increased occupational exposure

    Up to 90% of cases result from occupational exposure

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    Pathogenesis

    The fungi are found in the soil and in decayingplants and wood

    The disease is typically contracted from trauma tothe lower extremities, particularly as a result ofnot wearing shoes

    The organism is introduced into the dermis orsubcutis via implantation.

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    CLINICAL FEATURES

    Usually presents as a papule or nodule on the leg,which progresses to form a verrucous orgranulomatous plaque

    Lesion may appear annular as the central portionresolves with scarring

    Several lesions may coalesce to form amultinodular mass, or multiple lesions may existas discrete islands scattered within unaffectedskin

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    CLINICAL FEATURES

    It is thought that autoinoculation, fromscratching, may be responsible for the spread ofinfection

    Only one extremity is typically affected.Sometimes, a subcutaneous nodule or tumor isthe presenting lesion

    Local or constitutional symptoms are not typical.

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    Annular and figurate

    plaques due to central

    clearing and scarringwith a verrucous surface

    on the arm (A) and a

    more granulomatous

    appearance on the leg

    (B).

    C Brown-colored

    sclerotic body within a

    mixed granulomatous

    and neutrophilic dermalinfiltrate.

    C, CourtesyofJennifer

    McNiffMD.

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    Pathology

    Pseudoepitheliomatous hyperplasia, intraepidermal abscesses, andsuppurative and granulomatous inflammation within the dermis arethe typical histologic findings

    Round, pigmented bodies, which are said to resemble copperpennies (6 to 12 mm), are present in the dermis, bothextracellularly and within giant cells

    These are unique to chromoblastomycosis and are also known as

    Medlar bodies or sclerotic bodies

    Detection of organisms via PCR of tissue samples has been reportedfor the more common species.

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    Differential Diagnosis

    Biopsy is indicated to exclude other granulomatousinfectious diseases such as

    Cutaneous tuberculosis,

    Tertiary syphilis, Blastomycosis or

    Leishmaniasis

    that may also have associated scarring

    Mycetoma is another implantation mycosis that commonlyaffects the lower extremity, but edema, draining sinusesand grains point to this diagnosis

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    If a biopsy is not feasible, a KOH examination

    of scrapings from a pigmented portion of the

    lesion is performed

    The presence of pigmentedMedlarbodies is

    diagnostic (excluding diagnoses such asblastomycosis), but hyphae may also be seen

    Culture growth (at 2530C) is slow and thedifferent genera produce fairly similar colonial

    morphologies

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    Major differences between genera are the microscopicfeatures, in particular the type of conidia produced inculture.

    3 majortypes ( CPR )

    Cladosporium-like (long branching side chainswith shield cells at branch points)

    Phialophora-like (conidia resemble overflowing

    buds in a vase)

    Rhinocladiella-like (overall configuration similar toa mascara brush).

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    Treatment

    Therapeutic options are limited

    Some authors have advocated heat therapy based on evidence that thecausative organisms will not grow at high temperatures

    For small lesions, surgical excision (plus systemic antifungal treatment) can beattempted

    5-Flucytosine combined with either oral thiabendazole, intravenousamphotericin B or an oral triazole has been reported to be efficacious.

    Itraconazole alone (200-400 mg/day) administered for at least 6 months hasproved promising, with up to 80-90% cure rates according to one author

    .

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    Treatment

    The newest triazole, voriconazole, may also proveto be beneficial

    In a small series, oral terbinafine (500 mg/day)given for at least 7 months was described aseffective

    Cryosurgery and the addition of antibiotics if thelesion is secondarily infected

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    THANK YOU