Ozkan Ferda, Bilgiç Remziye, Cesur Suna
Department of Pathology, Yeditepe University, Istanbul, Turkey.
APMIS. 2006 Jul-Aug;114(7-8):562-5. doi: 10.1111/j.1600-0463.2006.apm_326.x.
A keratoacanthoma of the vulva in a 33-year-old woman is described. The patient presented with a rapidly growing exophytic lesion of 1 cm in diameter over the clitoris that had been present for a couple of months. An excisional biopsy was performed. Pathologic examination of the exophytic nodule showed squamous proliferation with a characteristic central keratin- filled crater. There were pushing margins. High power microscopy showed squamous cells of cytologically bland appearance with glassy cytoplasm. There were few mitotic figures. Less than 10% Ki-67-positive staining nuclei were seen. There was no p53 oncoprotein overexpression. Keratoacanthoma of the vulva is rare with only five cases having been reviewed in the English literature since 1985. Keratoacanthomas are rapidly growing crateriform lesions on the sun-exposed skin of the elderly. Because of its rarity in the vulva, the lesion can be misinterpreted as a malignant lesion such as squamous cell carcinoma. Awareness of vulvar occurrence of keratoacanthoma and its characteristic histopathologic features will help avoid misdiagnosis of a squamous cell carcinoma leading to radical surgery.
本文描述了一名33岁女性的外阴角化棘皮瘤。患者阴蒂上出现一个直径1厘米、迅速生长的外生性病变,已存在数月。进行了切除活检。对该外生性结节的病理检查显示鳞状上皮增生,有特征性的中央充满角蛋白的火山口。切缘呈推挤状。高倍显微镜下可见鳞状细胞,细胞学表现平淡,细胞质呈玻璃样。有少量有丝分裂象。可见不到10%的Ki-67阳性染色核。无p53癌蛋白过表达。外阴角化棘皮瘤罕见,自1985年以来英文文献中仅报道过5例。角化棘皮瘤是老年人暴露于阳光下皮肤处迅速生长的火山口状病变。由于其在外阴罕见,该病变可能被误诊为恶性病变,如鳞状细胞癌。认识到外阴发生角化棘皮瘤及其特征性组织病理学特征将有助于避免将鳞状细胞癌误诊而导致根治性手术。