SUBCUTANEOUS MYCOSIS INTRODUCTION Usually follow trauma. Lesions develop at the site of implantation of the etiological agent in the subcutaneous tissue. Includes – Mycetoma - Sporotrichosis - Rhinosporidiosis - Chromoblastomycosis - Phaeohyphomycosis - Lobomycosis MYCETOMA (=Maduromycosis=Madura foot) Mycetoma - clinical syndrome of localized, indolent, deforming, swollen lesions and sinuses, involving cutaneous and subcutaneous tissues, fascia, and bone; usually occurring on the foot or hand) etiologic agent may be fungi or actinomycetes. Madura foot referring to the first case seen in Madura region of India which was in the foot of that patient Infection is acquired following trauma to the skin by plant materials from trees, shrubs or vegetation debris, thus more seen in rural areas (in farmers walking bare-foot in agricultural land or city parks). One potential causal agent can be Pseudallescheria boydii, a soil/water inhabiting fungus with worldwide distribution. However other fungi can be involved. MYCETOMA (=Maduromycosis=Madura foot) Fungi associated with fungal mycetoma are opportunistic. mycotic mycetoma - usually more common in men (3:1 to 5:1) than in women usually results from trauma or puncture wounds to feet, legs, arms and hands (usually on the feet) starts out as tumor-like to subcutaneous swelling ruptures near the surface; infects deeper tissues including subcutaneous tissues and ligaments (tendons, muscles and bone are usually spared) small particles or grains leak out of the lesions - these represent the yellowish microcolonies Mycetoma MYCETOMA (=Maduromycosis=Madura foot) Posttraumatic chronic inf. of subcutaneous tissue Common in tropical climates Causative agents Saprophytic fungi (Eumycetoma) Actinomyces (Actinomycetoma) MYCETOMA Causative agents Madurella mycetomatis Pseudallescheria boydii Acremonium Exophiala jeanselmei Leptosphaeria Aspergillus The common etiological agent in Saudi Arabia and neighboring countries are: Madurella mycetomatis causes the majority of the cases with the black grains. It is imperfect dematiaceous mold with brown colonies and diffused honeycolord pigment. Madurella grisea: another species of madurella similar to mycetomatis but with grey colonies Pseudoallescheria boydii: causes white grain mycetoma. It is Ascomycetes mold forming cleistothecia and ascospores. The imperfect of it’s the moniliaceous mold: Scedosporium apiospermum which forms annelloconidia from annellids. Synnemata and conidia MYCETOMA Clinical findings Site(s): Feet, lower extremities, hands Findings: Abscess formation, draining sinuses containing granules Deformities Dissemination: Muscles and bones MYCETOMA Diagnosis Clinical findings are nonspecific Identification of the infecting fungus is difficult Characteristics of the granule, colony morphology, and physiological tests are used for identification EUMYCETOMA Treatment Surgery Antifungal therapy Amphotericin B Flucytosine Topical nystatin Topical potassium iodide (choice of treatment varies according to the infecting fungus) SPOROTRICHOSIS Caused by Sporothrix schenckii, a dimorphic fungus. Most common in USA. Found on plant, thorns & timber Infection is acquired through thorn pricks or other minor injuries Pathogenesis & pathology Spreads from primary site to the regional LNs through lymphatics Mostly involves upper limbs Clinical features - Nodules on the skin, subcutaneous tissue and in the LNs which later soften & ulcerate. Lymphocutaneous sporotrichosis Laboratory Diagnosis Specimens – pus, exudate & aspirate from nodules. - curettage or swabs from open lesions. Direct Examination Gram’s stain – gram+ve, irregularly stained yeast cells. CFW – very useful. Direct examination Tissues – organisms appear as cigar shaped bodies (yeast cells) 3-5µ in diameter. “Asteroid bodies” in the lesion – central fungus cell surrounded by a refractile eosinophilic halo, called “ Splendore-Hoeppli” phenomenon : due to immune complex deposition around the organism. Culture Inoculated on 2 sets of SDA, BHIA Incubated at 25°& 37°C. Smear from Culture septate hyphae - very thin & carry flower like clusters of small conidia on delicate sterigmata. Treatment & Prophylaxis Saturated solution of KI – drug of choice Oral Ketoconazole or Itraconazole RHINOSPORIDIOSIS Caused by a hydrophilic Rhinosporidium seeberi protist, 1st identified in Argentina, but majority of cases occur in India and Srilanka. High incidence among people who frequently bath along with domestic animals in ponds, tanks, lakes Clinical Features Chronic granulomatous disease of mucous membrane. Characterised by the development of friable polyps in the nose, mouth or eye. Miscellaneous forms – Buccal cavity,vagina, vulva, penis, urethra or rectum Laboratory Diagnosis Cannot be cultured Direct Examination FNAC (fine needle aspiration Biopsy of lesion, Nasal washing - Contains sporangia filled with thousands of sporangiospores(6-9µ) embedded in a stroma of connective tissue & capillaries cytology), Treatment & Prophylaxis Radical Surgery:- Excision/ Electrocautery Medical therapy :- not useful DDS (diaminodiphenylsulfone; widely used) Recurrence common CHROMO BLASTOMYCOSIS Caused by dematiaceous (pigmented) fungi Commonest fungi - Fonsecaea Species Phialophora verrucosa Cladosporium carrionii Also called as Verrucous dermatitis Chromoblastomycosis Clinical features Soil saprobes enter the skin by traumatic implantation and lesions develop slowly around the site of implantation Warty cutaneous nodules which resembles flouts of cauliflower - Verrucous dermatitis Frequently ulcerate Confined to the subcutaneous tissue of the feet and lower legs Laboratory Diagnosis Direct Examination 1. Dry crusty material from the surface of the lesions KOH w/m – dark brown, multicellular structures, 5-12μ in diameter that divide by transverse septation. -Called sclerotic bodies, medlar bodies, copperpennies bodies or muriform cells Fonsecaea spp. Phialophora spp. Sclerotic bodies - KOH Sclerotic bodies - tissues Direct examination Medlar bodies - characteristic tissue form facilitates survival of organism in host tissues. 2. Tissue Stains - for Biopsy specimens HE, Giemsa & Fontana- Masson - Sclerotic bodies very well seen Fungal culture - SDA with actidione and antibiotics Treatment & Prophylaxis Responds poorly to available therapies. Cryotherapy, Thermotherapy, therapy,Chemotherapy and Surgery. Flucytosine (commonly used drug) Itraconazole, Fluconazole, Terbinafine *Relapses are frequently seen Laser PHAEOHYPHOMYCOSIS Seen in debilitated & immunodeficient hosts. Causes subcutaneous & systemic infection. Caused by dematiaceous fungi. Commonest genera involved - Alternaria, Bipolaris, Curvularia, Exophiala, Phialophora, etc. Cutaneous phaeohyphomycosis of the forearm caused by Exophiala jeanselmei. Cutaneous phaeohyphomycosis of the face caused by Wangiella dermatitidis. Phaeohyphomycosis Exophiala moniliae Wangiella dermatitidis Cladophialophora bantiana Bipolaris australiensis Cladosporium cladosporioides Aureobasidium pullulans Clinical Features 1. 2. 3. Clinical types: Brain abscess caused by Cladosporium Subcutaneous or intramuscular lesions with abscess or cysts - single circumscribed lesion with a central cavity filled with pus and surrounded by a fibrous wall Cutaneous lesions Laboratory Diagnosis Specimen Aspirates from cysts Curetting from plaques, nodules and drained abscess Direct Examination KOH mount - Pigmented hyphae 3-4µ in dia. Fungal Culture SDA with actidione at 25º & 37ºC. Treatment & Prophylaxis Local excision for subcutaneous forms Invasive infections – I.V. AMB + Flucytosine. Oral LOBOMYCOSIS Caused by Lacazia loboi (Hydrophilic fungus) : exists only as yeast cells. Involves exposed parts Presence of macule, papule, keloid, verrucous, nodular lesions or plaques & tumors. Lesions are painless with slight pruritis Laboratory Diagnosis • Direct Examination of curettage / biopsy crushed a. KOH w / m b. CFW - spheroid, yeast - like cells, 5 -12µ - thick - walled & multinucleate. - form chain with cells joined by bridges. c. HE – may show ‘asteroid bodies’ Culture – cannot be cultured Fontana Masson stain Treatment & prophylaxis No effective medical treatment Complete excision Cryosurgery.