Fibrosing Colonopathy Presenting in a Patient with Cystinosis.

Dominic Fiore, Vidhur Sohini, Elizabeth Mileti, Nicholas Fiore
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Abstract

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.

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以胱氨酸病患者为例的纤维化结肠病。
纤维化性结肠病是一种独特的病理特征,以长节段狭窄为特征,通常发生在回盲区。历史上,它最常见于囊性纤维化(CF)患者。纤维化性结肠病被认为是继发于过量的外源性脂肪酶药物。这种情况在过去十年中很少见。在这个病例中,纤维化结肠病是在一个患有胱氨酸病溶酶体贮积症的病人中发现的。纤维化性结肠病以前未在胱氨酸病患者中发现。患者因出血性腹泻进行结肠镜检查时发现结肠穿孔后出现纤维化结肠病。本病例报告的目的是提请注意一个值得注意的病例纤维化结肠病患者谁没有囊性纤维化,而是胱氨酸病。
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