Serpa-Irizarry Miguel, Ruiz-Medina Pedro, Del Valle-Segarra Antonio, Zequeira-Diaz Jorge
General Surgery, University of Puerto Rico, Medical Sciences Campus, San Juan, PRI.
General Surgery, University of Puerto Rico Medical Sciences Campus, San Juan, PRI.
Cureus. 2024 Sep 11;16(9):e69158. doi: 10.7759/cureus.69158. eCollection 2024 Sep.
Coats plus syndrome (CPS) is an exceedingly rare genetic disorder associated with premature telomere shortening. The syndrome, also known as cerebroretinal microangiopathy with calcifications and cysts, has a multisystemic manifestation. It may present as brain abnormalities, seizures, osteopenia, prenatal and postnatal growth deficiency, and portal hypertension, among others. Up to 40% of affected individuals manifest recurrent gastrointestinal (GI) bleeding which can be life-threatening in some cases. Treatment for GI bleeding is not standardized and is therefore individualized based on the patient's clinical status, comorbidities, and resource availability. We herein present a case of a 20-year-old female with CPS and a two-year history of severe recurrent GI bleeding unable to be identified by conventional endoscopy. This report highlights successful laparoscopic assisted enteroscopy with enterectomy as a novel diagnostic and therapeutic modality in this population.
科茨加综合征(CPS)是一种极其罕见的与端粒过早缩短相关的遗传性疾病。该综合征,也被称为伴有钙化和囊肿的脑视网膜微血管病,具有多系统表现。它可能表现为脑部异常、癫痫发作、骨质减少、产前和产后生长发育迟缓以及门静脉高压等。高达40%的受影响个体出现反复的胃肠道(GI)出血,在某些情况下可能危及生命。胃肠道出血的治疗尚未标准化,因此需根据患者的临床状况、合并症和资源可用性进行个体化治疗。我们在此报告一例20岁患有科茨加综合征的女性病例,其有两年严重反复胃肠道出血病史,常规内镜检查无法明确病因。本报告强调了腹腔镜辅助小肠镜检查联合肠切除术作为该人群一种新型诊断和治疗方式的成功应用。