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Poroid Hidradenoma: Case Report and Comprehensive Review of the Literature.
Brooks, Arrin; Morris, Mariah; Cuda, Jonathan; Rahimpour, Armein; Munie, Semeret.
Afiliação
  • Brooks A; Joan C Edwards School of Medicine, Marshall University, Huntington, WV, USA.
  • Morris M; Department of Surgery, West Virginia University School of Medicine, Morgantown, WV, USA.
  • Cuda J; Joan C Edwards School of Medicine, Marshall University, Huntington, WV, USA.
  • Rahimpour A; Department of Dermatopathology, Marshall Health, Cabell Huntington Hospital, Huntington, WV, USA.
  • Munie S; Department of General Surgery, Joan C Edwards School of Medicine, Huntington, WV, USA.
Case Rep Dermatol ; 15(1): 202-216, 2023.
Article em En | MEDLINE | ID: mdl-37928337
ABSTRACT
Poroid hidradenoma (PH) is a rare benign adnexal tumor of eccrine differentiation. It is the rarest of the four described variants of poroid neoplasms. PHs characteristically share a hybrid of the architectural features of the hidradenoma, namely, tumor cells are entirely intradermal with both solid and cystic components, and the cytologic characteristics of the poroid neoplasms, containing predominantly poroid and cuticular cells. Many published reports of PH since its original discovery in 1990 state that "very few" cases of PH can be found in the literature. Here, we have identified a total of 75 published accounts of PH, including the case presented here, as well as the associated patient demographics, lesion characteristics, treatment, and outcomes. We suggest that while uncommon, PH is likely not exceptionally rare and could be an underreported diagnosis.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article