{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,4,8]],"date-time":"2026-04-08T23:40:48Z","timestamp":1775691648123,"version":"3.50.1"},"reference-count":9,"publisher":"Oxford University Press (OUP)","issue":"6","license":[{"start":{"date-parts":[[2024,10,12]],"date-time":"2024-10-12T00:00:00Z","timestamp":1728691200000},"content-version":"vor","delay-in-days":387,"URL":"https:\/\/creativecommons.org\/licenses\/by\/4.0\/"}],"funder":[{"name":"This article received no specific grant from any funding agency in the public, commercial, or not-for-profit sectors"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2023,12,1]]},"abstract":"<jats:title>Abstract<\/jats:title>\n               <jats:p>Pilomatrixoma is a benign hair follicle tumour. Anetodermic changes overlying pilomatrixoma are rare. The aim of this study is to evaluate a case series of patients with a clinical diagnosis of anetodermic pilomatrixoma presenting to our Dermatology Department over a 5-year period. Eight cases were identified. The median age of onset was 21 years. All cases presented on the upper limbs and trunk with a solitary rapidly evolving tumour, tender on palpation. They had an erythematous protuberant appearance with a wrinkled and atrophic surface. Underlying pilomatrixomas were firm measuring 1\u20135 cm. Simple excision was carried out in seven cases without postoperative complications. In conclusion, anetodermic pilomatrixoma is a rare variant of this tumour, occurring more frequently on the upper body. It presents with identifiable features and should be differentiated from other skin tumours. Surgical removal is usually the gold standard treatment.<\/jats:p>","DOI":"10.1002\/ski2.284","type":"journal-article","created":{"date-parts":[[2023,9,22]],"date-time":"2023-09-22T06:16:32Z","timestamp":1695363392000},"source":"Crossref","is-referenced-by-count":3,"title":["Anetodermic Pilomatrixomas: A Case Series"],"prefix":"10.1093","volume":"3","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-9217-4109","authenticated-orcid":false,"given":"Evangelia","family":"Vetsiou","sequence":"first","affiliation":[{"name":"Department of Dermatology, Addenbrooke's Hospital, Cambridge University Hospitals NHS Foundation Trust , Cambridge ,","place":["UK"]}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Julia","family":"Gass","sequence":"additional","affiliation":[{"name":"Department of Dermatology, Addenbrooke's Hospital, Cambridge University Hospitals NHS Foundation Trust , Cambridge ,","place":["UK"]}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Andre","family":"Khoo","sequence":"additional","affiliation":[{"name":"Department of Dermatology, Addenbrooke's Hospital, Cambridge University Hospitals NHS Foundation Trust , Cambridge ,","place":["UK"]}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Sarah","family":"McDonald","sequence":"additional","affiliation":[{"name":"Department of Histopathology, Addenbrooke's Hospital, Cambridge University Hospitals NHS Foundation Trust , Cambridge ,","place":["UK"]}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Niki","family":"Stefanos","sequence":"additional","affiliation":[{"name":"Department of Histopathology, Addenbrooke's Hospital, Cambridge University Hospitals NHS Foundation Trust , Cambridge ,","place":["UK"]}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Ed","family":"Rytina","sequence":"additional","affiliation":[{"name":"Department of Histopathology, Addenbrooke's Hospital, Cambridge University Hospitals NHS Foundation Trust , Cambridge ,","place":["UK"]}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Nigel","family":"Burrows","sequence":"additional","affiliation":[{"name":"Department of Dermatology, Addenbrooke's Hospital, Cambridge University Hospitals NHS Foundation Trust , Cambridge ,","place":["UK"]}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"286","published-online":{"date-parts":[[2023,9,21]]},"reference":[{"issue":"4","key":"2025010818111802600_ski2284-bib-0001","doi-asserted-by":"publisher","first-page":"e41","DOI":"10.1097\/DAD.0b013e31823583f5","article-title":"Anetodermic pilomatricoma: molecular characteristics and trauma in the development of its bullous appearance","volume":"34","author":"Li","year":"2012","journal-title":"Am J Dermatopathol"},{"issue":"3","key":"2025010818111802600_ski2284-bib-0002","doi-asserted-by":"publisher","DOI":"10.5070\/d3233034296","article-title":"Anetodermic pilomatricoma: clinical, histopathologic, and sonographic findings","volume":"23","author":"V\u00e1zquez-Osorio","year":"2017","journal-title":"Dermatol Online J"},{"issue":"1","key":"2025010818111802600_ski2284-bib-0003","doi-asserted-by":"publisher","first-page":"9","DOI":"10.1111\/pde.13947","article-title":"Syndromes association with multiple pilomatricomas. 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