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A primary cutaneous adenoid-cystic carcinoma in a young woman. Differential diagnosis and clinical implications
Author(s) -
Claudio Cacchi,
Severino Persechino,
Laura Fidanza,
Armando Bartolazzi
Publication year - 2011
Publication title -
rare tumors
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.285
H-Index - 15
eISSN - 2036-3613
pISSN - 2036-3605
DOI - 10.4081/rt.2011.e3
Subject(s) - medicine , scalp , adenoid cystic carcinoma , histogenesis , differential diagnosis , nodule (geology) , cribriform , adenoid , wide local excision , dermatology , pathology , carcinoma , paleontology , immunohistochemistry , biology
Primary cutaneous adenoid cystic carcinoma (PCACC) is a rare slow-growing neoplasm of disputed histogenesis characterized by a cribriform pattern at histology and local aggressive behaviour. Up to date about 60 cases of PCACC have been reported in the literature. This tumour is most common in the scalp, affects middle-aged and older individuals (mean age 59) and has predilection for women. We describe an unexpected case of PCACC in a 32-years-old woman referred to our clinic for a subcutaneous nodule in the scalp showing a slow growth and indolent course. The differential diagnosis and the clinical management of this PCACC patient, successfully treated with a wide local excision, are presented and discussed

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