Bell Lisa Dillon, Bernat John A, Rahhal Riad
University of Iowa Carver College of Medicine, Iowa City, IA 52242, USA.
Division of Medical Genetics and Genomics, University of Iowa Stead Family Children's Hospital, Iowa City, IA 52242, USA.
Gastroenterology Res. 2022 Feb;15(1):33-38. doi: 10.14740/gr1480. Epub 2022 Jan 10.
In the following clinical case of infantile juvenile polyposis syndrome (JPS), administration of a pharmacologic agent sirolimus was associated with reduced disease burden without need for bowel resection. The positive impact included improvement in protein-losing enteropathy, decreased intestinal blood loss, and improved weight gain. In addition, the number of polyps resected per unit time and frequency of upper and lower endoscopic evaluation needed dropped after initiation of sirolimus. This case report describes a positive clinical outcome and discusses the use of sirolimus with aggressive polypectomy as a potential treatment for the rare disease entity of polygenic infantile JPS. Through this case, we aim to emphasize that while administration of this drug may mitigate many sequelae of infantile JPS, it does not appear to eliminate the need for aggressive polypectomy.
在以下这例小儿幼年性息肉病综合征(JPS)的临床病例中,给予药物西罗莫司可减轻疾病负担,而无需进行肠切除术。其积极影响包括蛋白丢失性肠病得到改善、肠道失血量减少以及体重增加。此外,开始使用西罗莫司后,单位时间内切除的息肉数量以及上下消化道内镜评估所需的频率均有所下降。本病例报告描述了一个积极的临床结果,并讨论了将西罗莫司与积极的息肉切除术联合使用作为多基因小儿JPS这种罕见疾病实体的一种潜在治疗方法。通过这个病例,我们旨在强调,虽然使用这种药物可能减轻小儿JPS的许多后遗症,但似乎并不能消除积极息肉切除术的必要性。