@Article{Soukup2016,
journal="Polish Journal of Pathology",
issn="1233-9687",
volume="67",
number="3",
year="2016",
title="Dermatofibroma-like granular cell tumour: a potential diagnostic pitfall",
abstract="Dermatofibroma-like granular cell tumour (GCT) is a rare entity, with only two cases having been described so far. We report another case in a 62-year-old woman, discuss histopathological features, and review other tumours in which granular changes have been observed. Our tumour was composed predominantly of oval-to-spindle granular cells with prominent nucleoli, arranged in short fascicles and storiform pattern, infiltrating around collagen bundles. Immunohistochemical analysis with antibodies against CD31, CD56, CD68, CD117, S-100 protein, inhibin, calretinin, EMA, p53 and MIB-1 was performed, showing expression of CD56, CD68, S-100 protein, inhibin and calretinin. The diagnosis of atypical dermatofibroma-like GCT was made.",
author="Soukup, Jiri
and Hadzi-Nikolov, Dimitar
and Ryska, Ales",
pages="291--294",
doi="10.5114/pjp.2016.63782",
url="http://dx.doi.org/10.5114/pjp.2016.63782"
}