Vale Rodrigues Rita, Santos Filipa, Pereira da Silva João, Francisco Inês, Claro Isabel, Albuquerque Cristina, Lemos Maria Manuel, Limbert Manuel, Dias Pereira António
Serviço de Gastrenterologia, Instituto Português de Oncologia de Lisboa Francisco Gentil, E.P.E., Rua Prof. Lima Basto, 1099-023, Lisbon, Portugal.
Serviço de Anatomia Patológica, Instituto Português de Oncologia de Lisboa Francisco Gentil, E.P.E., Lisbon, Portugal.
Fam Cancer. 2017 Apr;16(2):267-270. doi: 10.1007/s10689-016-9941-1.
Multiple gastrointestinal stromal tumors (GISTs) caused by germline KIT gene mutations are an extremely rare autosomal dominant disorder. We report a case of a 21-year-old woman who presented to the emergency department with a 2-week history of asthenia, palpitations and upper gastrointestinal bleeding. After further clinical evaluation one gastric and two small bowel GISTs were diagnosed, which were surgically resected after neoadjuvant therapy with Imatinib. Diffuse hyperplasia of the interstitial cells of Cajal was also seen in the background gastric and small intestinal walls. Somatic mutational analysis of the KIT gene revealed a substitution at codon 576 in exon 11 (p.Leu576Pro) in all tumors and normal ileal mucosa. The germline nature of this mutation was confirmed by mutation analysis in peripheral blood leukocytes. However, she had no familial history of GISTs and her parents did not carry the respective germline mutation.
由种系KIT基因突变引起的多发性胃肠道间质瘤(GIST)是一种极其罕见的常染色体显性疾病。我们报告了一例21岁女性病例,该患者因乏力、心悸和上消化道出血2周病史就诊于急诊科。经过进一步临床评估,诊断出一个胃GIST和两个小肠GIST,在使用伊马替尼进行新辅助治疗后进行了手术切除。在背景胃和小肠壁中也观察到 Cajal间质细胞的弥漫性增生。对KIT基因的体细胞突变分析显示,所有肿瘤和正常回肠黏膜中外显子11的密码子576处存在替代(p.Leu576Pro)。通过外周血白细胞的突变分析证实了该突变的种系性质。然而,她没有GIST家族史,其父母也未携带相应的种系突变。