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人类白细胞抗原部分匹配的同胞中的菊池-藤本病:家族易感性的病例研究

Kikuchi-Fujimoto Disease in Human Leukocyte Antigen Partially Matched Siblings: A Case Study of Familial Susceptibility.

作者信息

Isoda Atsushi, Tahara Kenichi, Ide Munenori

机构信息

Department of Hematology, Iryohojin Hoshiiin, Maebashi, JPN.

Department of Hematology, Maebashi Red Cross Hospital, Maebashi, JPN.

出版信息

Cureus. 2023 Dec 23;15(12):e51010. doi: 10.7759/cureus.51010. eCollection 2023 Dec.

Abstract

Kikuchi-Fujimoto disease (KFD) is a rare and self-limiting disorder that predominantly affects young individuals of Asian descent. This case report describes familial KFD in partially human leukocyte antigen (HLA)-matched siblings. An adolescent male presented with cervical lymphadenopathy and elevated lactate dehydrogenase (LDH) levels, diagnosed by biopsy as KFD; approximately one year later, his sister presented with similar symptoms. Both siblings were found to carry the HLA-DPB1*0202 allele, which is commonly associated with KFD. These cases highlight a genetic component in KFD and encourage further genetic research to delineate the pathogenesis of the disease.

摘要

菊池-藤本病(KFD)是一种罕见的自限性疾病,主要影响亚洲血统的年轻人。本病例报告描述了部分人类白细胞抗原(HLA)匹配的兄弟姐妹中的家族性KFD。一名青少年男性出现颈部淋巴结病和乳酸脱氢酶(LDH)水平升高,经活检诊断为KFD;大约一年后,他的妹妹出现了类似症状。发现这对兄弟姐妹都携带HLA-DPB1*0202等位基因,该等位基因通常与KFD相关。这些病例突出了KFD中的遗传成分,并鼓励进一步开展基因研究以阐明该疾病的发病机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ebd2/10803893/dc956577793a/cureus-0015-00000051010-i01.jpg

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