Premium
CD34‐positive glomus tumor: clinicopathologic and immunohistochemical analysis of six cases with myxoid stromal changes
Author(s) -
Mentzel Thomas,
Hügel Heino,
Kutzner Heinz
Publication year - 2002
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.1600-0560.2002.290706.x
Subject(s) - glomus tumor , pathology , cd34 , vimentin , immunohistochemistry , glomus cell , stromal cell , biology , medicine , receptor , stem cell , biochemistry , genetics , chemoreceptor
Background: Glomus tumors are benign, mainly superficially located perivascular neoplasms, composed of cytologically characteristic neoplastic cells staining immunohistochemically positive for vimentin and muscle actin, closely associated with often branching blood vessels. Methods: Six cases of glomus tumor were analysed histologically and immunohistochemically. Results: We report six cases of glomus tumor (three solid glomus tumors, two glomangiomas, one glomangiomyoma) arising on the fingers of adult patients (five female and one male patient; age range 35–65 years) that showed prominent myxoid stromal changes and immunohistochemically a coexpression of alpha‐smooth muscle actin and CD34 by neoplastic cells. Conclusions: Neoplastic cells in glomus tumor may show a coexpression of alpha‐smooth muscle actin and CD34, an important finding regarding the differential diagnosis of these lesions and the relationship of perivascular neoplasms.