RESUMO
AIM: To document a case of lobomycosis and to discuss its epidemiology & diagnosis. CASE REPORT: A 53-year-old male presented with a history of nasal congestion, nasal discharge, and epistaxis following Covid 19 infection. On physical examination, there was necrotic slough in the nasal vestibule near the inferior turbinate. Scrapings and punch biopsy were taken from the lesion. Hematoxylin-eosin-stained sections showed necrotic and mucoid areas with mixed inflammatory cell infiltration and numerous budding yeasts 3- 7µm diameter in singles, and small clusters with single narrow based budding as well as multiple budding including sequential budding forming "chains of yeasts". A diagnosis of Lobomycosis was made. Yeasts of lobomycosis are often confused with other yeasts such as P. brasiliensis, Candida spp., B. dermatitidis, and Cryptococci, but characteristic 'sequential budding' with a 'chain of yeasts" aid in the final diagnosis. Demonstration of yeasts with characteristic chains either in tissue sections or in potassium hydroxide (KOH) preparation of scraped material, exudate, or exfoliative cytology is the mainstay in the diagnosis as the organisms are uncultivable in vitro in culture medium.
Assuntos
COVID-19 , Lobomicose , Masculino , Humanos , Pessoa de Meia-Idade , Lobomicose/diagnóstico , Lobomicose/patologia , COVID-19/complicações , Pele/patologia , BiópsiaRESUMO
Chondroblastoma of squamous part of temporal bone is a very rare bone tumor. Although most of them are benign, the prognosis is not predictable. A 14-year-old girl presented with recurrent slowly growing mass over the right side of the temporo-parietal region of skull vault. Initial curettage material showed extensive chondroid areas and diagnosed histologically as "enchondroma." Histology of completely excised recurrent mass showed identifiable chondroblastic foci. She was followed up for 3 years and was free from recurrence. Chondroblastomas at very rare sites such as squamous part of temporal bone have variable histology, confusing with other giant cell lesions, variable prognosis, and require prompt diagnosis and complete excision.