一名患有自身免疫性多腺体综合征的年轻女性四肢部分脂肪营养不良 1.

JCEM case reports Pub Date : 2024-09-24 eCollection Date: 2024-10-01 DOI:10.1210/jcemcr/luae166
Shubham Agarwal, Aaron Bodansky, Chao Xing, Mark S Anderson, Abhimanyu Garg
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引用次数: 0

摘要

自身免疫性多腺体综合征 1(APS1)是一种常染色体隐性遗传疾病,由自身免疫调节剂(AIRE)基因中的双倍致病变体引起,表现为慢性皮肤粘膜念珠菌病、原发性甲状旁腺功能减退症和肾上腺功能不全。我们报告了一名患有 APS1 的 39 岁女性,她在成年后出现了部分脂肪营养不良。她在婴儿期因念珠菌病和甲状旁腺功能减退症出现尿布疹、口腔鹅口疮和四肢抽搐。童年时期,她患上了甲状腺功能减退症、原发性肾上腺功能不全和卵巢功能不全。14 岁时,由于多次抗生素难治性真菌感染,她接受了同胞匹配的异基因骨髓移植。35 岁时,她的血清甘油三酯为 914 mg/dL(10.32 mmol/L),上下肢和臀部皮下脂肪减少。全身双能 X 射线吸收测定显示,她的下肢脂肪含量低于第一百分位数。对从唾液中提取的DNA进行全外显子组测序发现了致病变体,即AIRE中的p.Leu28Pro和p.Arg257*,但没有发现已知的脂肪营养不良基因。噬菌体免疫沉淀测序显示,患者体内存在MAGEB1、MAGEB4和RFX6的自身抗体,这些抗体以前曾在APS1中出现过。我们的病例表明,APS1 患者可能会因为针对新型脂肪细胞表达蛋白的自身抗体而出现部分脂肪营养不良。我们的患者体内针对脂肪组织表达的ODC1、NUCKS1或FNBP1L的高水平自身抗体与脂肪营养不良之间的因果关系仍不确定。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Partial Lipodystrophy Affecting the Extremities in a Young Woman With Autoimmune Polyglandular Syndrome 1.

Autoimmune polyglandular syndrome 1 (APS1) is an autosomal recessive disorder due to biallelic pathogenic variants in the autoimmune regulator (AIRE) gene that manifests with chronic mucocutaneous candidiasis, primary hypoparathyroidism, and adrenal insufficiency. We report a 39-year-old woman with APS1 who developed partial lipodystrophy during adulthood. She presented with diaper rashes, oral thrush, and tetany during infancy due to candidiasis and hypoparathyroidism. During childhood, she developed hypothyroidism, primary adrenal insufficiency, and ovarian insufficiency. At age 14, she received a sibling-matched allogenic bone marrow transplant due to multiple antibiotic-refractory fungal infections. At age 35, her serum triglycerides were 914 mg/dL (10.32 mmol/L) and she had loss of subcutaneous fat from the upper and lower extremities and hips. A whole-body dual-energy x-ray absorptiometry revealed lower-extremity fat at less than the first percentile. Whole-exome sequencing on DNA extracted from saliva revealed pathogenic variants, p.Leu28Pro and p.Arg257* in AIRE but none in the known lipodystrophy genes. Phage-immunoprecipitation-sequencing revealed the presence of autoantibodies to MAGEB1, MAGEB4, and RFX6, which have been previously reported in APS1. Our case suggests that patients with APS1 may develop partial lipodystrophy due to autoantibodies against novel adipocyte-expressed proteins. A causal relationship of high levels of autoantibodies in our patient to adipose tissue-expressed ODC1, NUCKS1, or FNBP1L and lipodystrophy remains uncertain.

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