Saftic Marina, Batinac Tanja, Zamolo Gordana, Coklo Miran, Simat Marina, Mustac Elvira, Bosnar Alan, Grahovac Blazenka
Department of Dermatovenerology, Clinical Hospital Center, Rijeka, Croatia.
Tumori. 2006 Jan-Feb;92(1):79-82. doi: 10.1177/030089160609200114.
Keratoacanthoma (KA) is a clinically distinct, rapidly growing lesion that generally presents as a solitary crateriform nodule in sun-exposed areas in elderly, fair-skinned individuals. A KA larger than 20-30 mm is referred to as giant keratoacanthoma, a relatively rare lesion especially in young patients. Such lesions grow rapidly with possible destruction of underlying tissues. In addition to ultraviolet exposure, KAs have also been associated with chemical carcinogens, chemical peels, genetic factors, chronic skin conditions that produce scarring, trauma and thermal burns. Immunosuppressed patients, especially after transplantation, also develop KAs. A viral etiology has been suggested but not confirmed. We encountered a case of giant keratoacanthoma (greater than 50 mm in diameter) with induration of underlying structures on the upper lip of a 39-year-old male sailor. The patient reported sudden appearance and rapid enlargement of the lesion in only three weeks. Biopsy of the cutaneous lesion and the characteristic clinical history suggested the diagnosis of keratoacanthoma. Total excision with primary closure of the defect by a nasolabial advancement flap was performed. Histological examination of the tumor mass confirmed the diagnosis of KA with infiltrative growth and perineural invasion. Immunosuppression was excluded by blood analyses, as were HIV, syphilis and hepatitis infections. Only low-risk genital HPV type 6 was detected in the lesion, suggesting a possible cocarcinogenic effect of HPV and UV light in a chronically sun-exposed patient.
角化棘皮瘤(KA)是一种临床上有明显特征、生长迅速的病变,通常表现为老年白皮肤个体日光暴露部位的孤立火山口状结节。直径大于20 - 30毫米的KA被称为巨大角化棘皮瘤,这是一种相对罕见的病变,尤其在年轻患者中。此类病变生长迅速,可能会破坏深层组织。除紫外线暴露外,KA还与化学致癌物、化学换肤、遗传因素、导致瘢痕形成的慢性皮肤疾病、创伤和热烧伤有关。免疫抑制患者,尤其是移植后患者,也会发生KA。曾有人提出病毒病因,但未得到证实。我们遇到一例巨大角化棘皮瘤(直径大于50毫米),发生于一名39岁男性水手的上唇,其深层结构有硬结。患者报告该病变仅在三周内突然出现并迅速增大。皮肤病变活检及典型临床病史提示角化棘皮瘤的诊断。通过鼻唇推进皮瓣对缺损进行一期缝合的完全切除手术得以实施。肿瘤块的组织学检查证实为KA,伴有浸润性生长和神经周围侵犯。血液分析排除了免疫抑制,同时也排除了HIV、梅毒和肝炎感染。病变中仅检测到低风险的生殖器HPV 6型,提示在长期日光暴露的患者中HPV和紫外线可能存在协同致癌作用。