Kumar Pallav, Zameer Mohammed Moinuddin, Chandrashekar Vinay, Rao Sanjay
Department of Pediatric Surgery, Mazumder Shaw Medical Center, Bengaluru, Karnataka, India.
J Indian Assoc Pediatr Surg. 2024 Sep-Oct;29(5):546-548. doi: 10.4103/jiaps.jiaps_51_24. Epub 2024 Aug 23.
Inflammatory myofibroblastic tumor (IMT) is a very rare tumor with still rare occurrence in the genitourinary system, presenting as a pelvic-ureteric junction (PUJ) obstruction (PUJO). We report a case of IMT at the PUJ mimicking congenital PUJO and review the relevant literature.
炎性肌纤维母细胞瘤(IMT)是一种非常罕见的肿瘤,在泌尿生殖系统中更为罕见,表现为肾盂输尿管连接部(PUJ)梗阻(PUJO)。我们报告一例发生在肾盂输尿管连接部的炎性肌纤维母细胞瘤,该病例酷似先天性肾盂输尿管连接部梗阻,并复习相关文献。