Subcutaneous phaeohyphomycosis: A rare case

Zahruddin Ahmad, - and Diah Mira Indramaya, - and Yuri Widia, - and Sylvia Anggraeni, - and Linda Astari, - and Evy Ervianti, - and Sunarso Suyoso, - (2019) Subcutaneous phaeohyphomycosis: A rare case. Dermatology Reports, 11 (S1). pp. 149-152. ISSN 20367406

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Abstract

Phaeohyphomycosis is a rare fungal infection caused by melanized fungi which usually involve the skin and subcutaneous tissue. It is an infrequent cause of infection in human beings. Common clinical manifestations are subcutaneous cystic swellings, which is localized, characterized by subcutaneous asymptomatic nodular lesions that develop after traumatic implantation of fungus from contaminated soil, thorns or wood splinters, especially on extremities. We report a case of subcutaneous phaeohyphomycosis presenting as multiple cystic swellings over the left lower leg with unknown predisposing factors. At first, the patient was misdiagnosed as soft tissue tumor and subcutaneous tuberculosis, then got surgical and anti-tuberculosis therapy respectively, but there was no improvement. Further investigation revealed granulomatous inflammation on histopathology examination and black-coloured colonies identifed as Exophiala dermatitidis on fungal culture. This case of phaeohyphomycosis was successfully treated by itraconazole monotherapy without surgical excision and still under follow-up.

Item Type: Article
Uncontrolled Keywords: Phaeohyphomycosis, subcutaneous, Exophiala dermatitidis
Subjects: R Medicine > R Medicine (General)
R Medicine > RL Dermatology
Divisions: 01. Fakultas Kedokteran > Ilmu Kesehatan Kulit dan Kelamin (Spesialis)
Creators:
CreatorsNIM
Zahruddin Ahmad, -UNSPECIFIED
Diah Mira Indramaya, -NIDN8898700016
Yuri Widia, -NIDN0006078406
Sylvia Anggraeni, -NIDN0022118405
Linda Astari, -NIDN0006038108
Evy Ervianti, -NIDN8840900016
Sunarso Suyoso, -UNSPECIFIED
Depositing User: arys fk
Date Deposited: 09 May 2023 00:46
Last Modified: 09 May 2023 00:46
URI: http://repository.unair.ac.id/id/eprint/126420
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