多种不同 KCNJ5 致病变体产生醛固酮的多发性微小结节

JCEM case reports Pub Date : 2024-11-20 eCollection Date: 2024-12-01 DOI:10.1210/jcemcr/luae213
Yasushi Oiwa, Ko Aiga, Mitsuhiro Kometani, Takahiro Asano, Mikiya Usukura, Takashi Yoneda
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引用次数: 0

摘要

原发性醛固酮增多症(PA)是继发性高血压的最常见形式。最近,对醛固酮分泌腺瘤(PA 的主要病因)的基因分析发现了几个致病基因。在此,我们介绍一例患有 PA 的 27 岁日本女性患者。她因高血压和低钾血症(血清钾为 2.8 mEq/L [2.8 mmol/L])转诊至我院。通过多项确诊检查,她被确诊为 PA。计算机断层扫描显示,两侧肾上腺均无明显肿瘤。肾上腺静脉取样显示右侧肾上腺醛固酮分泌过多。手术后,她的血压恢复正常,低钾血症也有所改善。病理结果显示有多个醛固酮分泌微小结节,直径为 KCNJ5。其中两个小结节具有 T158A 致病变异,1 个具有 G151R 致病变异,1 个没有 KCNJ5 基因致病变异。总之,在我们的病例中,1 个肾上腺出现了多个结节,并发现了遗传异质性。术后 17 年,左侧肾上腺未见复发。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Aldosterone-producing Multiple Micronodules With Several Different KCNJ5 Pathogenic Variants.

Primary aldosteronism (PA) is the most common form of secondary hypertension. Recently, the genetic analysis of aldosterone-producing adenoma, a major cause of PA, has revealed several causative genes. Herein, we present a case of a 27-year-old Japanese female with PA. She was referred to our hospital with hypertension and hypokalemia (serum potassium, 2.8 mEq/L [2.8 mmol/L]). PA was diagnosed using several confirmatory tests. Computed tomography showed no apparent tumor in either adrenal gland. Adrenal vein sampling showed aldosterone overproduction in the right adrenal gland. Laparoscopic right adrenalectomy was performed, her blood pressure normalized, and the hypokalemia improved after surgery. Pathological findings revealed multiple aldosterone-producing micronodules with diameters of <5 mm. DNAs were extracted from 4 different micronodules and analyzed for KCNJ5. Two micronodules had a T158A pathogenic variant, 1 had a G151R pathogenic variant, and 1 had no pathogenic variant in the KCNJ5 gene. In summary, in our case, multiple nodules were present in 1 adrenal gland, and genetic heterogeneity was identified. No recurrence on the left side has been observed over 17 years following the surgery.

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