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Epidermodysplasia verruciformis–associated eccrine neoplasm: a rare entity with distinctive clinical and histopathologic features.

Authors :
Russell-Goldman, Eleanor
Baranov, Esther
Siegmund, Stephanie
Yang, Catherine S.
Laga, Alvaro C.
Hanna, John
Source :
Virchows Archiv: European Journal of Pathology; Mar2024, Vol. 484 Issue 3, p423-427, 5p
Publication Year :
2024

Abstract

Most tumors are caused by inherited or acquired genetic changes. However, a subset of tumors is driven by viral infection including Kaposi sarcoma, nasopharyngeal carcinoma, and others. Human papillomavirus (HPV) is an especially common cause of epithelial cancers and hyperplasias. Epidermodysplasia verruciformis (EDV) is a rare type of HPV infection with characteristic histopathologic features and a unique spectrum of HPV subtypes. We report here a distinctive form of EDV-associated eccrine neoplasia. Seven tumors from two patients were analyzed and show highly uniform features including multiple clustered clinical lesions, multifocal epidermal origin, eccrine differentiation with close association with the acrosyringium, an anastomosing growth pattern, and a bland monotonous poroid-to-basaloid cytomorphology. Clinical follow-up for one patient has been benign to date. These tumors show strong similarity to two previously reported cases, suggesting that this type of EDV-associated eccrine neoplasia may represent a rare but reproducible form of skin adnexal tumor with distinctive clinicopathologic features. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
09456317
Volume :
484
Issue :
3
Database :
Complementary Index
Journal :
Virchows Archiv: European Journal of Pathology
Publication Type :
Academic Journal
Accession number :
176627668
Full Text :
https://doi.org/10.1007/s00428-024-03785-w