| Literature DB >> 23091581 |
Evangelia Papadavid1, Maria Dalamaga, Irini Kapniari, Ekaterini Pantelidaki, Sotirios Papageorgiou, Vassiliki Pappa, Panagiotis Tsirigotis, Ioannis Dervenoulas, Nikolaos Stavrianeas, Dimitrios Rigopoulos.
Abstract
BACKGROUND: Lobomycosis, also known as Jorge Lobo's disease, represents a rare chronic subcutaneous mycosis caused by the fungus Lacazia loboi, an organism that is found within lesions but has not been cultured to date. The natural reservoir of L. loboi is unknown but it is believed to be aquatic, or associated with soil and vegetation. More than 550 human cases have been reported, especially in patients with a history of travel or residence in endemic areas (Central and South America, particularly Brazil) or in communities along rivers. MAIN OBSERVATIONS: We describe a 64-year-old Greek female farmer living in a coastal region, who presented with an erythematous plaque on her left inner thigh resembling a keloid. The diagnosis was based on the triad: 1) absence of fungal growth in cultures, 2) positive direct microscopic examination of the lesion and 3) histopathology, all consistent with lobomycosis. Particularly, skin biopsy showed deep cutaneous fungal infection with granulomatous reaction. Fungal cells were found inside giant cells. The fungi were thick-walled with some budding, isolated or in short chains. Dermal fibrosis was present. Our patient had a medical history of common variable immunodeficiency but no history of travel to South or Central America. She probably acquired this rare infection by injury during her agricultural works.Entities:
Keywords: Lacazia loboi; Lobo’s disease; immunodeficiency; infection; lacaziosis; lobomycosis; mycosis
Year: 2012 PMID: 23091581 PMCID: PMC3470791 DOI: 10.3315/jdcr.2012.1104
Source DB: PubMed Journal: J Dermatol Case Rep ISSN: 1898-7249