Gallina Nicole Compagnoni, Galvão Bárbara, Buffo Thais Helena, Stelini Rafael Fantelli, Magalhães Renata Ferreira, Leal Raquel Franco
Colorectal Surgery Unit, School of Medical Sciences, University of Campinas, Campinas, São Paulo, Brazil.
Department of Dermatology, School of Medical Sciences, University of Campinas, Campinas, São Paulo, Brazil.
Int J Surg Case Rep. 2025 Sep;134:111717. doi: 10.1016/j.ijscr.2025.111717. Epub 2025 Jul 22.
Metatypical carcinoma is a rare morphological variant of basal cell carcinoma (BCC) exhibiting histopathological features of both basal and squamous cell carcinomas. BCC's histologic subtypes are distinguished by a higher risk of local recurrence and a more aggressive clinical course. Its occurrence in sun-protected areas, such as the perianal and perineal regions, is uncommon and poses significant diagnostic and therapeutic challenges. Clinicians must know these atypical presentations to ensure timely and effective treatment, leading to better patient outcomes.
We present a case of a 74-year-old male who sought medical attention for an ulcerated lesion in the anterior perineal area, near the anal sphincter and base of the right scrotum. Histopathological examination of an incisional biopsy revealed a pigmented, nodular form of metatypical basal cell carcinoma, a rare presentation in an atypical location. Although basal cell carcinoma is a common skin malignancy, the lesion's location and histological subtype are unusual. The patient underwent surgical excision and a VY advancement flap closure, preserving both function and aesthetic appearance.
Metatypical BCC, arising in less visible or protected body areas, often escapes early detection, increasing the risk of local tissue invasion and recurrence. Early diagnosis through dermoscopy or imaging techniques such as MRI and high-resolution ultrasound is crucial for assessing disease extent. Treatment options may include conventional excision or Mohs micrographic surgery.
We reported an uncommon case of metatypical BCC, for which surgical resection and skin flap reconstruction resulted in a favorable outcome.
化生型癌是基底细胞癌(BCC)一种罕见的形态学变异型,兼具基底细胞癌和鳞状细胞癌的组织病理学特征。基底细胞癌的组织学亚型以局部复发风险较高和临床病程更具侵袭性为特征。其发生于如肛周和会阴区域等防晒部位的情况并不常见,给诊断和治疗带来重大挑战。临床医生必须了解这些非典型表现,以确保及时有效的治疗,从而改善患者预后。
我们报告一例74岁男性患者,其因会阴前部靠近肛门括约肌和右侧阴囊底部的溃疡性病变前来就医。切开活检的组织病理学检查显示为色素沉着的结节型化生型基底细胞癌,在非典型部位出现这种情况较为罕见。尽管基底细胞癌是一种常见的皮肤恶性肿瘤,但该病变的位置和组织学亚型并不寻常。患者接受了手术切除及VY推进皮瓣闭合术,保留了功能和美观。
化生型基底细胞癌发生于较难看到或受保护的身体部位,常难以早期发现,增加了局部组织侵袭和复发的风险。通过皮肤镜检查或MRI及高分辨率超声等成像技术进行早期诊断对于评估疾病范围至关重要。治疗选择可能包括传统切除术或莫氏显微外科手术。
我们报告了一例罕见的化生型基底细胞癌病例,手术切除及皮瓣重建取得了良好效果。