Menon Dipika, Dentel John N, Sanil Yamuna, Lawrence David
Division of Pediatric Cardiology, Children's Hospital of Michigan, School of Medicine - Wayne State University, Detroit, Michigan, United States.
Division of Cardiovascular Surgery, Children's Hospital of Michigan, School of Medicine - Wayne State University, Detroit, Michigan, United States.
J Pediatr Genet. 2021 Jan 12;12(2):171-174. doi: 10.1055/s-0040-1722287. eCollection 2023 Jun.
Nevoid basal cell carcinoma syndrome (NBCCS), also referred to as Gorlin's syndrome, is an autosomal dominant inherited condition that predisposes affected individuals to various tumors such as cardiac fibromas. Though technically benign, cardiac fibromas may result in malignant arrhythmias and sudden death. The pertinent literature pertaining to pediatric cases of cardiac fibromas and their clinical features were reviewed. We present the case of an asymptomatic teenage with de novo NBCCS who was diagnosed with both NBCCS and cardiac fibroma later in life. The patient was noted to have clinically significant ventricular arrhythmias that were eliminated with tumor resection. There are no established best practice guidelines for the management of cardiac fibromas in patients with NBCCS. Given the risk of sudden arrhythmic death, the presence of ventricular arrhythmias should prompt strong consideration of tumor resection.
痣样基底细胞癌综合征(NBCCS),也称为戈林综合征,是一种常染色体显性遗传疾病,使受影响个体易患各种肿瘤,如心脏纤维瘤。虽然从技术上讲心脏纤维瘤是良性的,但可能会导致恶性心律失常和猝死。我们回顾了有关小儿心脏纤维瘤病例及其临床特征的相关文献。我们报告了一例无症状的青少年新发NBCCS病例,该患者在后来的生活中被诊断出患有NBCCS和心脏纤维瘤。该患者被发现有具有临床意义的室性心律失常,肿瘤切除后心律失常消失。对于NBCCS患者心脏纤维瘤的管理,目前尚无既定的最佳实践指南。鉴于存在心律失常性猝死的风险,室性心律失常的出现应促使强烈考虑肿瘤切除。