黑斑–息肉综合征(Peutz-Jeghers Syndrome) 1例个案报道
A Case Report of Peutz-Jeghers Syndrome
DOI: 10.12677/acm.2026.1662403, PDF,   
作者: 黄嘉玥:西安医学院研究生院,陕西 西安;张 艳*:陕西省人民医院放射科,陕西 西安
关键词: 黑斑–息肉综合征STK11基因错构瘤性息肉锯齿状腺瘤青少年Peutz-Jeghers Syndrome STK11 Gene Hamartomatous Polyp Serrated Adenoma Adolescent
摘要: 本文报道1例16岁女性黑斑–息肉综合征(PJS)患者的临床诊疗过程,根据其皮肤黏膜特征、影像学表现、胃肠镜、病理结果及基因检测确诊。通过本病例分析,旨在提高临床对PJS典型表现与诊疗流程的认识,强调长期随访与多学科协作的重要性。
Abstract: This article reports the clinical diagnosis and treatment process of a 16-year-old female patient with Peutz-Jeghers Syndrome (PJS). The diagnosis was finally confirmed by genetic testing, combined with the patient’s mucocutaneous characteristics, gastrointestinal symptoms, imaging findings, as well as results of gastroenteroscopy and pathology. Through the analysis of this case, this article aims to improve clinicians’ understanding of the typical manifestations and diagnosis-treatment process of PJS, and emphasize the importance of long-term follow-up and multidisciplinary collaboration.
文章引用:黄嘉玥, 张艳. 黑斑–息肉综合征(Peutz-Jeghers Syndrome) 1例个案报道[J]. 临床医学进展, 2026, 16(6): 1847-1853. https://doi.org/10.12677/acm.2026.1662403

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