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DGAT1 相关腹泻伴脂毒性相关的凋亡性肠病、谷胶不耐受和 IBD 样炎症:17 岁患者病例报告及文献复习。

Apoptotic enteropathy, gluten intolerance, and IBD-like inflammation associated with lipotoxicity in DGAT1 deficiency-related diarrhea: a case report of a 17-year-old patient and literature review.

机构信息

Department of Pathology, Ghent University Hospital, C. Heymanslaan 10, 9000, Ghent, Belgium.

Center for Medical Genetics, Ghent University Hospital, 9000, Ghent, Belgium.

出版信息

Virchows Arch. 2022 Nov;481(5):785-791. doi: 10.1007/s00428-022-03365-w. Epub 2022 Jun 28.

DOI:10.1007/s00428-022-03365-w
PMID:35763111
Abstract

We present a long-term follow-up in a 17-year-old girl with DGAT1-related diarrhea, an autosomal recessive disorder characterized by impaired triglyceride absorption. Neonatal presentation included severe congenital diarrhea, protein-losing enteropathy, and failure to thrive requiring total parenteral nutrition. Duodenal biopsies revealed apoptotic enteropathy and acute inflammation with the presence of macrophages and Touton giant cells, related to the intake of fat. She was able to switch to enteral nutrition on a fat-free diet. However, at age 10, she developed gluten-induced enteropathy and then IBD-like inflammation 5 years later. Immunohistochemistry was able to confirm the diagnosis, while DGAT1 sequencing remained inconclusive. This highlights the role of histopathology and immunohistochemistry, despite the increasing importance of genetic analysis in the diagnostic work-up. This report also illustrates that parenteral nutrition weaning is possible in DGAT1-related diarrhea, but gut barrier dysfunction might increase the risk of autoimmune intestinal disease.

摘要

我们报告了一例 17 岁女孩的长期随访结果,该患者患有 DGAT1 相关腹泻,这是一种常染色体隐性疾病,其特征是甘油三酯吸收受损。新生儿期表现为严重的先天性腹泻、蛋白丢失性肠病和生长不良,需要全胃肠外营养。十二指肠活检显示凋亡性肠病和急性炎症,伴有巨噬细胞和 Touton 巨细胞,与脂肪摄入有关。她能够在无脂肪饮食的情况下切换到肠内营养。然而,在 10 岁时,她出现了麦胶蛋白相关性肠病,5 年后又出现了类似 IBD 的炎症。免疫组织化学能够确诊该病,而 DGAT1 测序结果仍不确定。这凸显了组织病理学和免疫组织化学的作用,尽管遗传分析在诊断中的重要性日益增加。本报告还表明,DGAT1 相关腹泻患者可以逐渐停止胃肠外营养,但肠道屏障功能障碍可能会增加自身免疫性肠道疾病的风险。

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DGAT1 mutations leading to delayed chronic diarrhoea: a case report.导致慢性腹泻延迟的 DGAT1 突变:病例报告。
BMC Med Genet. 2020 Dec 1;21(1):239. doi: 10.1186/s12881-020-01164-1.
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Genetic variants in DGAT1 cause diverse clinical presentations of malnutrition through a specific molecular mechanism.DGAT1基因变异通过特定分子机制导致营养不良的多种临床表现。
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Phenotype and Genotype of a Cohort of Chinese Children with Early-Onset Protein-Losing Enteropathy.
一名儿科患者中与先天性腹泻相关的二酰甘油酰基转移酶1(DGAT1)突变:病例报告
Cureus. 2024 Jul 22;16(7):e65119. doi: 10.7759/cureus.65119. eCollection 2024 Jul.
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Case report: Diagnosis and treatment of DGAT1 deficiency-induced congenital diarrhea in two cases and literature review.病例报告:两例DGAT1缺乏所致先天性腹泻的诊断与治疗及文献复习
Front Pediatr. 2023 Oct 16;11:1253800. doi: 10.3389/fped.2023.1253800. eCollection 2023.
中国早发性蛋白丢失性肠病患儿的表型和基因型。
J Pediatr. 2019 May;208:38-42.e3. doi: 10.1016/j.jpeds.2018.12.003. Epub 2019 Mar 8.
4
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5
Autoimmune enteropathies.自身免疫性肠病
Virchows Arch. 2018 Jan;472(1):55-66. doi: 10.1007/s00428-017-2243-7. Epub 2017 Oct 11.
6
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