光化性角化病作为原发性多发性同步鳞状细胞皮肤癌的预测因子:一个临床病例

T. Sedova
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摘要

我们报告一位84岁的原发性多发性同步高分化角化性鳞状细胞皮肤癌患者,同时伴有多发性光化性角化病和光化性唇炎。临床病例是一个独特的同时发展的原发多发性鳞状细胞癌的鼻尖和下唇朱红色区在一个病人过去的职业和太阳负担,轻表型,和慢性光损伤的迹象的皮肤。经临床、皮镜及超声检查发现患者有光化性角化病的征象,并经病理形态学检查证实。发现了光化性角化病发生恶性转化的危险因素,如多发病灶和病史长。光化区的恶性转化表现为直径超过1cm的快速进展的溃疡区,明显的角化过度,炎症和下层组织浸润,出血和疼痛增加。需要强调的是,明确和鉴别诊断需要对皮肤活检样本进行病理形态学评估。本病例提示多灶性光化性角化病患者应接受皮肤科医生的终身随访,并强制治疗和预防措施。
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Actinic keratosis as a predictor of primary multiple synchronous squamous cell skin cancer: a clinical case
We present a clinical case of a primary multiple synchronous highly differentiated keratinizing squamous cell skin cancer in an 84-year old patient with multiple actinic keratosis and actinic cheilitis. The clinical case is unique for the simultaneous development of primary multiple squamous cell carcinoma of the tip of the nose and the vermilion zone of the lower lip in a patient with a past occupational and solar burden, a light phenotype, and signs of chronic photo injury the skin. Clinical, dermatoscopic and sonographic signs of keratotic actinic keratosis were identified in the patient and confirmed by pathomorphological examination. The risk factors for malignant transformation of actinic keratosis were found, such as multiple efflorescences and a long disease history. The malignant transformation of the actinic areas manifested as rapidly progressive ulceration zones more than 1 cm in diameter, pronounced hyperkeratosis, inflammation and infiltration of the underlying tissues, increased bleeding and pain. It is to be underlined that definitive and differential diagnosis requires pathomorphological assessment of the skin biopsy sample. This clinical case indicates that patients with multiple foci of actinic keratosis should be under a lifelong follow-up by dermatovenereologists, with mandatory treatment and prevention measure.
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