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Atypical fibroxanthoma with prominent sclerosis
Author(s) -
Bruecks Andrea K.,
Medlicott Shaun A.,
Trotter Martin J.
Publication year - 2003
Publication title -
journal of cutaneous pathology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.597
H-Index - 75
eISSN - 1600-0560
pISSN - 0303-6987
DOI - 10.1034/j.1600-0560.2003.00077.x
Subject(s) - atypical fibroxanthoma , pathology , hyaline , dermatofibrosarcoma protuberans , giant cell , medicine , lesion , cd68 , cd99 , vimentin , immunohistochemistry
Background: Malignant cutaneous spindle cell lesions with marked sclerosis are uncommon. Only a few cases of cutaneous leiomyosarcoma and dermatofibrosarcoma protuberans with sclerosis have been published. Methods: We report a case of atypical fibroxanthoma (AFX) with prominent sclerosis and hyalinization occurring on the scalp of an 81‐year‐old male. Results: Histopathologic examination revealed an exophytic, well‐delineated, focally ulcerated tumor arising in sun‐damaged skin. The lesion was composed of atypical spindle cells arranged in a fascicled and vaguely storiform pattern. Occasional multinucleated giant cells were present. The tumor cells were strongly positive for CD99 (O13), vimentin, and smooth muscle actin, and focally positive for CD68. There was striking sclerosis with hyalinization throughout the lesion. Conclusions: Rarely, AFX may exhibit marked sclerosis with areas of complete replacement of tumor by hyalinized collagen. In a small biopsy, such hyalinization may be a diagnostic pitfall leading to an erroneous diagnosis.