戈林-戈尔茨综合征病例报告

Y. Bennaoui, A. Jaifi, Msk Hattab, Samir Maidame, Aziz Zakaria, N. Hattab
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引用次数: 0

摘要

戈林-戈尔茨综合征,又称基底细胞痣综合征。这种疾病有多种临床表现,包括多发性皮肤病变和其他系统异常。本病例是一名 32 岁的男性,无明显病史,因多发痣病变转诊至我院进行评估。临床检查发现,右侧鼻唇沟上部有三处皮损,右侧脸颊下部有一处皮损,左侧鼻唇沟有一处皮损,下巴、右太阳穴和右侧脸颊上还有疑似皮损。本病例强调了识别戈林-戈兹综合征各种表现的重要性,这有助于对这种遗传性疾病进行早期诊断和治疗。进一步的调查和长期随访对于了解这种疾病的进展和治疗至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Case Report of Gorlin-Goltz Syndrome
Gorlin-Goltz syndrome, also known as basal cell nevus syndrome. This condition is characterized by various clinical manifestations, including multiple cutaneous lesions and other systemic abnormalities. We present the case of a 32-year-old man with no significant medical history who was referred to our institution for evaluation of multiple budding lesions. Clinical examination revealed three lesions in the upper right nasolabial fold, one in the lower right cheek, one in the left nasolabial fold, and additional suspect lesions on the chin, right temple, and right cheek. This case underscores the importance of recognizing the diverse manifestations of Gorlin-Goltz syndrome, which can aid in early diagnosis and management of this inherited disorder. Further investigation and long-term follow-up are essential for understanding the progression and management of this condition.
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