Fiore Dominic, Sohini Vidhur, Mileti Elizabeth, Fiore Nicholas
From the Pediatric Surgery Associates, Touro University Nevada, College of Osteopathic Medicine, Las Vegas, Nevada.
Department of General Surgery, Valley Health Systems GME, Las Vegas, Nevada.
JPGN Rep. 2023 Jun 9;4(3):e321. doi: 10.1097/PG9.0000000000000321. eCollection 2023 Aug.
Fibrosing colonopathy is a unique pathology characterized by long segment stricture, usually of the ileocecal region. Historically, it is most commonly described in patients with cystic fibrosis (CF). Fibrosing colonopathy is felt to be secondary to excessive doses of exogenous lipase medication. This condition is rarely seen in the last decade. In this case presentation, fibrosing colonopathy was identified in a patient with the lysosomal storage disorder of cystinosis. Fibrosing colonopathy has not previously been described in patients with cystinosis. The patient was found to have fibrosing colonopathy after perforation of the colon during a colonoscopy for bloody diarrhea. This case report aims to draw attention to a noteworthy case of fibrosing colonopathy in a patient who does not have cystic fibrosis, but rather cystinosis.
纤维性结肠病是一种独特的病理学表现,其特征为长节段狭窄,通常累及回盲部。从历史上看,它最常见于囊性纤维化(CF)患者。纤维性结肠病被认为是外源性脂肪酶药物剂量过大所致。在过去十年中,这种情况很少见。在本病例报告中,一名患有胱氨酸贮积症(一种溶酶体贮积病)的患者被诊断出患有纤维性结肠病。此前,纤维性结肠病在胱氨酸贮积症患者中尚未有过描述。该患者因便血性腹泻接受结肠镜检查时发生结肠穿孔,随后被发现患有纤维性结肠病。本病例报告旨在引起对一名并非患有囊性纤维化而是患有胱氨酸贮积症的患者发生纤维性结肠病这一值得关注病例的注意。