Evidence map›Paper›PMID 42609852›Full record

ArticleClinical, cosmetic and investigational dermatology2026

Atypical Fibroxanthoma on the Scalp of a 74-Year-Old Male with an Incidental Finding of an Amelanotic Melanoma on the Back.

Iwona Chlebicka, Martyna Byrska, Klaudia Knecht-Gurwin, Ambika Pradhan, Aleksandra Stefaniak, Zdzisław Woźniak, Patrycja Łazicka, Jacek C Szepietowski

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In one paragraph

Article in Clinical, cosmetic and investigational dermatology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

The trial behind it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Iwona ChlebickaDepartment of Dermato-Venereology, 4th Military Hospital, Wroclaw, Poland.
Martyna ByrskaDepartment of General and Oncological Dermatology, Jan Mikulicz University Hospital, Wroclaw, Poland.
Klaudia Knecht-GurwinDepartment of Dermato-Venereology, 4th Military Hospital, Wroclaw, Poland.
Ambika PradhanDepartment of Dermatology, Jigme Dorji Wangchuck National Referral Hospital, Thimphu, Bhutan.
Aleksandra StefaniakDepartment of General and Oncological Dermatology, Jan Mikulicz University Hospital, Wroclaw, Poland.
Zdzisław WoźniakFaculty of Medicine and Faculty of Cosmetology, Calisia University, Kalisz, Poland.
Patrycja ŁazickaDepartment of General, Transplant and Liver Surgery, Independent Public Central Clinical Hospital, Warsaw, Poland.ORCID 0009-0000-9018-8155
Jacek C SzepietowskiDepartment of Dermato-Venereology, 4th Military Hospital, Wroclaw, Poland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Atypical fibroxanthoma (AFX) is a rare spindle-cell tumor of the skin, typically occurring in sun-exposed areas of elderly patients. We report an unusual case of synchronous AFX and amelanotic melanoma in a 74-year-old man. The patient presented with a 7-month history of a bleeding nodule on the scalp. Clinical examination revealed an 18 mm red nodule in diameter with hemorrhagic crust. An additional 23 mm pink-red bleeding nodule in diameter on the back, previously unnoticed by the patient, was also identified. Both lesions were excised with 3-5 mm margins. Histopathological and immunohistochemical analysis of the scalp tumor showed a dermal proliferation of atypical spindle cells with high mitotic activity, Ki-67 expression of approximately 35%, SMA positivity, and negativity for melanocytic and epithelial markers, supporting the diagnosis of AFX. In contrast, the second lesion demonstrated melanocytic markers (Melan A, HMB-45, S-100 positivity), with Breslow thickness of 1 mm and Clark level III, consistent with amelanotic melanoma. The patient was referred for further surgical oncological management. At the last available follow-up, 6 months after excision, the patient showed no clinical evidence of local recurrence, nodal involvement, or distant metastasis. This case highlights the importance of thorough skin examination in patients with cutaneous tumors, as multiple distinct malignancies may coexist.

Indexed as

amelanotic melanomaatypical fibroxanthomaskin neoplasmsspindle-cell tumorsynchronous tumors

Identifiers

PMID42609852
PMCPMC13479085

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