Jebrini Nidal, Dwaik Majed, Jaber Mohanad, Jabari Sami, Razem Raghad, Sarahna Man, Alzaro Rashad, Aljabari Feras, Aqel Mohamed, Sarahneh Husein
Hemato-Oncology Department, Faculty of Medicine, Palestine Polytechnic University, Hebron, State of Palestine.
Dean's Office, Faculty of Medicine, Palestine Polytechnic University, Hebron, State of Palestine.
Case Rep Dermatol Med. 2025 Mar 26;2025:7801944. doi: 10.1155/crdm/7801944. eCollection 2025.
Epidermodysplasia verruciformis (EV), a rare hereditary skin disorder linked to HPV immunity, increases the risk of squamous cell carcinoma (SCC), typically in sun-exposed areas. This case highlights an extraordinary instance of SCC in a Sun-shielded region, marking the second documented case globally. The medical records and histopathological slides of the case were retrospectively reviewed. This work has been reported based on the CARE criteria. A 28-year-old Palestinian woman, who adheres to a sun-protective Hijab due to her Muslim faith and has limited sun exposure working in a clothing store, with painful scalp lesions presented at the dermatology clinic. She and her siblings were diagnosed with EV. Three years ago, a painful, enlarging lesion on her scalp led to a diagnosis of trichoblastic carcinoma, followed by the development of six similar lesions. A year later, she returned with multiple painful, pus-producing lesions exhibiting features of trichoblastic and verrucous carcinoma, posing a challenging clinical scenario. EV is a rare genetic skin disorder linked to EVER1/TCM6 or EVER2/TCM8 gene mutations, causing widespread warts due to specific HPV types. It heightens the risk of nonmelanoma skin cancer (NMSC), mainly SCC, often associated with beta-HPVs 5 and 8. Notably, atypical cases challenge the sun-exposure SCC concept. The reatment involves UV protection, retinoids, and close monitoring, critical to prevent lesion recurrence and aggressive malignancy interventions upon therapy discontinuation. In this unique case, a patient with EV developed SCC in an uncommonly sun-protected skin area, highlighting the extreme rarity of such an event within the context of this condition's complications.
疣状表皮发育不良(EV)是一种与HPV免疫相关的罕见遗传性皮肤病,会增加鳞状细胞癌(SCC)的风险,通常发生在阳光暴露部位。本病例突出了一例发生在防晒区域的SCC特殊病例,是全球第二例有记录的此类病例。对该病例的病历和组织病理学切片进行了回顾性分析。本研究已按照CARE标准进行报告。一名28岁的巴勒斯坦女性,由于其穆斯林信仰,坚持佩戴防晒头巾,且在服装店工作,阳光暴露有限,因头皮疼痛性病变就诊于皮肤科诊所。她和她的兄弟姐妹被诊断为EV。三年前,她头皮上出现一个疼痛且不断增大的病变,诊断为毛母质癌,随后又出现了六个类似病变。一年后,她再次就诊,出现多个疼痛、有脓性分泌物的病变,具有毛母质癌和疣状癌的特征,构成了具有挑战性的临床情况。EV是一种罕见的遗传性皮肤病,与EVER1/TCM6或EVER2/TCM8基因突变有关,由于特定的HPV类型导致广泛的疣。它会增加非黑素瘤皮肤癌(NMSC)的风险,主要是SCC,通常与β - HPV 5和8相关。值得注意的是,非典型病例对阳光暴露与SCC的概念提出了挑战。治疗包括紫外线防护、维甲酸类药物以及密切监测,这对于预防病变复发以及在治疗中断时进行积极的恶性肿瘤干预至关重要。在这个独特的病例中,一名患有EV的患者在一个罕见的防晒皮肤区域发生了SCC,凸显了在这种疾病并发症背景下此类事件的极端罕见性。