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婴儿早期直肠阴道瘘的罕见病因:基因所致!

A Rare Cause of Rectovaginal Fistula in Early Infancy: It is in the Genes!

作者信息

Swaminathan Aravind, Sathiyasekaran Malathi, Padankatti Swathi, Padankatti Rajiv B, Arulprakash S, Raj Revathi

机构信息

Department of Pediatrics, MGM Healthcare, Chennai, Tamil Nadu, India.

Department of Gastroenterlogy, MGM Healthcare, Chennai, Tamil Nadu, India.

出版信息

J Indian Assoc Pediatr Surg. 2021 Nov-Dec;26(6):442-444. doi: 10.4103/jiaps.JIAPS_217_20. Epub 2021 Nov 12.

Abstract

Acquired Rectovaginal Fistula (RVF) is rare in infants. Interleukin10/ Interleukin 10 receptor deficiencies are monogenic disorders presenting as aggressive forms of infantile onset inflammatory bowel disease with perianal abscess and fistula. Genetic studies assist in confirming the diagnosis. We present a two month old infant with rectovaginal fistula, severe colitis, failure to thrive and recurrent infections in whom colonoscopy revealed irregular colonic ulcers, and genetic studies confirmed an IL10RB mutation. Hematopoietic Stem cell transplantation is the definitive therapy for this disorder which the child underwent. We report this infant with an acquired RVF with extraintestinal features due to IL10RB mutation to highlight the importance of thinking beyond the local anatomy and looking into the genetic domain.

摘要

获得性直肠阴道瘘(RVF)在婴儿中较为罕见。白细胞介素10/白细胞介素10受体缺陷是一种单基因疾病,表现为侵袭性婴儿期起病的炎症性肠病,并伴有肛周脓肿和瘘管。基因研究有助于确诊。我们报告了一名两个月大的婴儿,患有直肠阴道瘘、严重结肠炎、发育不良和反复感染,结肠镜检查发现结肠溃疡不规则,基因研究证实存在IL10RB突变。造血干细胞移植是该疾病的确定性治疗方法,该患儿接受了此治疗。我们报告了这名因IL10RB突变而患有具有肠外特征的获得性RVF的婴儿,以强调超越局部解剖结构并深入研究基因领域的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d2a4/8637981/018e2daf1a44/JIAPS-26-442-g001.jpg

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