Departments of Pediatric Gastroenterology, Hepatology and Nutrition, Dr. Sami Ulus Obstetrics and Gynecology, Children's Health and Disease Training and Research Hospital, Ankara, Turkey.
Departments of Pediatric Oncology and Hematology, Dr. Sami Ulus Obstetrics and Gynecology, Children's Health and Disease Training and Research Hospital, Ankara, Turkey.
Turk J Pediatr. 2022;64(4):766-774. doi: 10.24953/turkjped.2021.5330.
PTEN hamartoma tumor syndrome (PHTS) is an umbrella term including Cowden syndrome (CS), Bannayan-Riley-Ruvalcaba syndrome (BRRS), PTEN-related Proteus syndrome (PS), and PTEN-related Proteus-like syndrome. One of the disorders in PHTS spectrum, CS is characterized by macrocephaly, mucocutaneous findings, gastrointestinal system (GIS) polyposis and an increased lifetime risk of GIS, breast, thyroid and other cancers.
In this study, we report an adolescent patient presenting with recurrent life-threatening upper GIS bleeding as a result of hamartomatous polyposis. Genetic studies revealed a known pathogenic nonsense mutation confirming the initial diagnosis of CS.
Additionally, we describe our therapeutic intervention to improve the patient`s clinical symptoms with sirolimus, which its use is infrequently addressed in the literature for pediatric age group harboring PTEN mutations.
PTEN 错构瘤肿瘤综合征 (PHTS) 是一个统称,包括考登综合征 (CS)、班纳扬-赖利-鲁瓦卡巴综合征 (BRRS)、PTEN 相关的庞贝病 (PS) 和 PTEN 相关的庞贝样综合征。PHTS 谱中的一种疾病 CS 以大头畸形、黏膜皮肤表现、胃肠道系统 (GIS) 息肉和 GIS、乳腺、甲状腺和其他癌症的终身风险增加为特征。
在这项研究中,我们报告了一名青少年患者,因错构瘤性息肉病反复发作危及生命的上 GIS 出血。遗传研究显示了一个已知的致病性无义突变,证实了 CS 的初步诊断。
此外,我们描述了我们的治疗干预措施,用西罗莫司改善患者的临床症状,其在携带 PTEN 突变的儿科年龄组中的应用在文献中很少被提及。