Two distinct pathogenic pathways of digital papillary adenocarcinoma - BRAF mutation or low-risk HPV infection
- PMID: 36756976
- DOI: 10.1111/cup.14386
Two distinct pathogenic pathways of digital papillary adenocarcinoma - BRAF mutation or low-risk HPV infection
Abstract
Digital papillary adenocarcinoma (DPA) is a rare neoplasm that can exhibit local recurrence and distant metastasis. We present a series of eight cases of DPA showing two distinct clinical presentations, morphologies, immunophenotypes, and molecular features. Four cases were characterized by painless, slow-growing nodules located on the digits. The lesions were small, well-defined, and confined in the dermis. Histopathologically, these tumors were composed of glandular structures lined by cuboidal epithelium with luminal papillary infoldings. Only rare mitotic figures and minimal squamoid differentiation were present, and cellular necrosis was absent. All four cases were positive for the BRAF V600E immunohistochemistry but negative for p16, low-risk and high-risk HPV in situ hybridization (ISH). In contrast, the remaining four cases were characterized by painful, rapidly growing masses on the digits. These four lesions were located in the deep dermis and consisted of a solid, tightly packed papillary architecture lined by atypical epithelioid cells with inconspicuous nucleoli. Cellular necrosis, numerous mitotic figures, and prominent squamoid differentiation were seen. All cases were negative for the BRAF V600E IHC. However, they showed strong, patchy to diffuse reactivity for p16 and were positive for low-risk HPV ISH and negative for high-risk HPV ISH. Our findings suggest that the current classification of DPA encompasses tumors that show two discrete pathogenic pathways - BRAF mutation or low-risk HPV infection. DPAs with low-risk HPV infection exhibit aggressive clinical features, high-grade morphology, marked squamoid differentiation, and wild-type BRAF. DPAs with BRAF V600E have less aggressive clinical features, low-grade morphologic findings, mild to absent squamoid differentiation, and negative HPV infection.
Keywords: digital papillary adenocarcinoma; extensive squamoid differentation; low-grade HPV infection; wild-type BRAF.
© 2023 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.
Comment in
-
Acral BRAF-mutated tubular adenoma should be distinguished from HPV42-related digital papillary adenocarcinoma.J Cutan Pathol. 2023 Jun;50(6):577-579. doi: 10.1111/cup.14430. Epub 2023 Apr 14. J Cutan Pathol. 2023. PMID: 37057379 No abstract available.
References
REFERENCES
-
- Suchak R, Wang WL, Prieto VG, et al. Cutaneous digital papillary adenocarcinoma: a clinicopathologic study of 31 cases of a rare neoplasm with new observations. Am J Surg Pathol. 2012;36(12):1883-1891. doi:10.1097/PAS.0b013e31826320ec
-
- Hsu HC, Ho CY, Chen CH, Yang CH, Hong HS, Chuang YH. Aggressive digital papillary adenocarcinoma: a review. Clin Exp Dermatol. 2010;35(2):113-119. doi:10.1111/j.1365-2230.2009.03490.x
-
- Altmann S, Damert HG, Klausenitz S, Infanger M, Kraus A. Aggressive digital papillary adenocarcinoma - a rare malignant tumor of the sweat glands: two case reports and a review of the literature. Clin Cosmet Investig Dermatol. 2015;8:143-146. doi:10.2147/CCID.S71323
-
- Kao GF, Helwig EB, Graham JH. Aggressive digital papillary adenoma and adenocarcinoma. A clinicopathological study of 57 patients, with histochemical, immunopathological, and ultrastructural observations. J Cutan Pathol. 1987;14(3):129-146.
-
- Gole G, Tati S, Deshpande A, Gole S. Aggressive digital papillary adenocarcinoma in a young female-a rare presentation. J Hand Microsurg. 2016;3(1):31-33. doi:10.1007/s12593-010-0028-1
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical
Research Materials