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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http://dx.doi.org/10.1159/000531052 | DOI Listing |
Cureus
September 2024
Surgery, Harlem Hospital Center, New York, USA.
Asian J Surg
September 2024
Gansu University of Chinese Medical, Lanzhou, China; The 940th Hospital of Logistics Support Force of Chinese People's Laberation Army, Lanzhou, 730000, China. Electronic address:
Cureus
January 2024
Pathology Department, Faculty of Medicine and Pharmacy, Mohammed VI University Hospital, Oujda, MAR.
Poroid hidradenoma represents an uncommon and benign tumor originating from skin adnexa. It falls under the category of sweet duct neoplasms, along with poromas. It affects the elderly population most frequently.
View Article and Find Full Text PDFIndian J Dermatol
January 2023
Pathologist, Department of Histopathology, Plus Care Internationals Private Limited, Mumbai, Maharashtra, India E-mail:
Am J Dermatopathol
February 2024
Anatomical Pathology, PathWest Laboratory Medicine, J Block QEII Medical Centre, Nedlands, Perth, Australia.
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