Disseminated cutaneous histoplasmosis in an immunocompetent adult
Histoplasmosis, a systemic mycosis caused by the dimorphic fungus Histoplasma capsulatum var capsulatum and Histoplasma capsulatum var duboisii is endemic to many parts of the world. The clinical manifestations range from acute or chronic pulmonary infection to a progressive disseminated disease. Af...
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doaj-11f88230d0e54ef7b71056bb6112f3622020-11-24T21:06:03ZengWolters Kluwer Medknow PublicationsIndian Journal of Dermatology0019-51541998-36112012-01-0157320620910.4103/0019-5154.96194Disseminated cutaneous histoplasmosis in an immunocompetent adultManoj HarnalikarVidya KharkarUday KhopkarHistoplasmosis, a systemic mycosis caused by the dimorphic fungus Histoplasma capsulatum var capsulatum and Histoplasma capsulatum var duboisii is endemic to many parts of the world. The clinical manifestations range from acute or chronic pulmonary infection to a progressive disseminated disease. After initial exposure to the fungus, the infection is self-limited and restricted to the lungs in 99% of healthy individuals. The remaining 1%, however, progress to either disseminated or chronic disease involving the lungs, liver, spleen, lymph nodes, bone marrow or rarely, the skin and mucous membranes. Mucocutaneous histoplasmosis is frequently reported in patients with acquired immune deficiency syndrome (AIDS), but it is rare in immunocompetent hosts. A 60-year-old male presented with asymptomatic swelling of the hard palate and crusted papules and nodules over the extremities, face and trunk. Clinically, the diagnoses of cutaneous cryptococcosis versus histoplasmosis was considered in this patient. A chest X-ray revealed hilar lymphadenopathy. Enzyme-linked immunosorbent assay (ELISA) for human immunodeficiency virus (HIV) was nonreactive. Skin biopsy revealed multiple tiny intracellular round yeast forms with a halo in the mid-dermis. Culture of the skin biopsy in Sabouraud′s dextrose agar showed colonies of Histoplasma capsulatum. Despite an investigation including no evidence of underlying immunosuppression was found, he was started on IV amphotericin-B (0.5 mg/kg/day). However, the patient succumbed to his disease 2 days after presentation. We report a rare case of disseminated cutaneous histoplasmosis in an immunocompetent individual.http://www.e-ijd.org/article.asp?issn=0019-5154;year=2012;volume=57;issue=3;spage=206;epage=209;aulast=HarnalikarHistoplasmosishistoplasma capsulatumimmunocompetentmucocutaneous lesions |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Manoj Harnalikar Vidya Kharkar Uday Khopkar |
spellingShingle |
Manoj Harnalikar Vidya Kharkar Uday Khopkar Disseminated cutaneous histoplasmosis in an immunocompetent adult Indian Journal of Dermatology Histoplasmosis histoplasma capsulatum immunocompetent mucocutaneous lesions |
author_facet |
Manoj Harnalikar Vidya Kharkar Uday Khopkar |
author_sort |
Manoj Harnalikar |
title |
Disseminated cutaneous histoplasmosis in an immunocompetent adult |
title_short |
Disseminated cutaneous histoplasmosis in an immunocompetent adult |
title_full |
Disseminated cutaneous histoplasmosis in an immunocompetent adult |
title_fullStr |
Disseminated cutaneous histoplasmosis in an immunocompetent adult |
title_full_unstemmed |
Disseminated cutaneous histoplasmosis in an immunocompetent adult |
title_sort |
disseminated cutaneous histoplasmosis in an immunocompetent adult |
publisher |
Wolters Kluwer Medknow Publications |
series |
Indian Journal of Dermatology |
issn |
0019-5154 1998-3611 |
publishDate |
2012-01-01 |
description |
Histoplasmosis, a systemic mycosis caused by the dimorphic fungus Histoplasma capsulatum var capsulatum and Histoplasma capsulatum var duboisii is endemic to many parts of the world. The clinical manifestations range from acute or chronic pulmonary infection to a progressive disseminated disease. After initial exposure to the fungus, the infection is self-limited and restricted to the lungs in 99% of healthy individuals. The remaining 1%, however, progress to either disseminated or chronic disease involving the lungs, liver, spleen, lymph nodes, bone marrow or rarely, the skin and mucous membranes. Mucocutaneous histoplasmosis is frequently reported in patients with acquired immune deficiency syndrome (AIDS), but it is rare in immunocompetent hosts. A 60-year-old male presented with asymptomatic swelling of the hard palate and crusted papules and nodules over the extremities, face and trunk. Clinically, the diagnoses of cutaneous cryptococcosis versus histoplasmosis was considered in this patient. A chest X-ray revealed hilar lymphadenopathy. Enzyme-linked immunosorbent assay (ELISA) for human immunodeficiency virus (HIV) was nonreactive. Skin biopsy revealed multiple tiny intracellular round yeast forms with a halo in the mid-dermis. Culture of the skin biopsy in Sabouraud′s dextrose agar showed colonies of Histoplasma capsulatum. Despite an investigation including no evidence of underlying immunosuppression was found, he was started on IV amphotericin-B (0.5 mg/kg/day). However, the patient succumbed to his disease 2 days after presentation. We report a rare case of disseminated cutaneous histoplasmosis in an immunocompetent individual. |
topic |
Histoplasmosis histoplasma capsulatum immunocompetent mucocutaneous lesions |
url |
http://www.e-ijd.org/article.asp?issn=0019-5154;year=2012;volume=57;issue=3;spage=206;epage=209;aulast=Harnalikar |
work_keys_str_mv |
AT manojharnalikar disseminatedcutaneoushistoplasmosisinanimmunocompetentadult AT vidyakharkar disseminatedcutaneoushistoplasmosisinanimmunocompetentadult AT udaykhopkar disseminatedcutaneoushistoplasmosisinanimmunocompetentadult |
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