The Diagnostic Challenge of Potassium-Wasting and Hypertension in Pregnancy: Lessons from a Geller Syndrome Workup.

IF 0.9 Q4 UROLOGY & NEPHROLOGY
Case Reports in Nephrology and Dialysis Pub Date : 2025-07-17 eCollection Date: 2025-01-01 DOI:10.1159/000547158
Justin David Tse, Ryan Lin, Jackson Wang
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引用次数: 0

Abstract

Introduction: Hypokalemia in pregnancy is usually attributed to benign causes, yet persistent hypokalemia with hypertension raises concerns for rare renal potassium-wasting disorders. Among these, Geller syndrome, a rare mineralocorticoid receptor mutation that can be activated by progesterone, can precipitate severe hypokalemia and hypertension unique to pregnancy due to heightened receptor sensitivity. This case underscores the need to recognize and systematically evaluate potassium-wasting syndromes in pregnancy to optimize outcomes and inform clinical decision-making.

Case presentation: We present a 33-year-old woman, G6P2, at 21w6d of gestation, presented with abdominal pain, marked hypokalemia (2.6 mEq/L), and systolic blood pressures in the 150s. She reported no previous history of hypertension or diuretic use and had no significant family history. Initial assessment excluded common etiologies, such as preeclampsia, prompting an expanded renal workup. Laboratory findings revealed profound renal potassium-wasting, evidenced by a trans-tubular potassium gradient of 11 and a urine potassium-to-creatinine ratio of 45, alongside low aldosterone levels, normal cortisol, and thyroid function. She experienced persistent hypokalemia despite aggressive repletion which led to suspicion of Geller syndrome. Continued potassium supplementation, dietary guidance, and fetal delivery eventually led to stable potassium levels.

Conclusion: This case highlights the diagnostic complexities of addressing refractory hypokalemia and hypertension in pregnancy, advocating for the consideration of rare etiologies like Geller syndrome. Although negative in this instance, the suspicion of Geller syndrome informed a meticulous diagnostic approach, underscoring the importance of a comprehensive evaluation and genetic counseling in similar presentations. Such awareness can enhance clinicians' diagnostic frameworks, equipping them to identify and manage rare syndromes if needed. By expanding the differential diagnosis for persistent hypokalemia and hypertension in pregnancy, this case underscores the potential for improved maternal-fetal outcomes through informed and targeted management strategies.

孕期缺钾和高血压的诊断挑战:来自盖勒综合征检查的经验教训。
妊娠期低钾血症通常归因于良性原因,然而持续性低钾血症伴高血压引起了对罕见肾耗钾疾病的关注。其中,盖勒综合征是一种罕见的矿皮质激素受体突变,可被黄体酮激活,由于受体敏感性增高,可导致妊娠期特有的严重低钾血症和高血压。本病例强调需要认识和系统地评估钾消耗综合征在妊娠优化结果和告知临床决策。病例介绍:我们报告了一名33岁的女性,G6P2,在妊娠21w6d时,表现为腹痛,明显的低钾血症(2.6 mEq/L),收缩压在150s左右。她没有高血压史或利尿剂使用史,也没有明显的家族史。初步评估排除常见病因,如先兆子痫,提示扩大肾脏检查。实验室结果显示严重的肾钾消耗,经肾小管钾梯度为11,尿钾与肌酐比值为45,醛固酮水平低,皮质醇和甲状腺功能正常。她经历了持续的低钾血症,尽管有侵略性的充血,导致怀疑盖勒综合征。持续补充钾,饮食指导和胎儿分娩最终使钾水平稳定。结论:本病例强调了难治性低钾血症和妊娠期高血压诊断的复杂性,提倡考虑罕见的病因,如盖勒综合征。虽然本例阴性,但对盖勒综合征的怀疑提示了细致的诊断方法,强调了在类似的报告中进行全面评估和遗传咨询的重要性。这种认识可以加强临床医生的诊断框架,使他们能够在必要时识别和管理罕见综合征。通过扩大妊娠期持续性低钾血症和高血压的鉴别诊断,本病例强调了通过知情和有针对性的管理策略改善母胎结局的潜力。
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来源期刊
CiteScore
1.20
自引率
0.00%
发文量
36
审稿时长
10 weeks
期刊介绍: This peer-reviewed online-only journal publishes original case reports covering the entire spectrum of nephrology and dialysis, including genetic susceptibility, clinical presentation, diagnosis, treatment or prevention, toxicities of therapy, critical care, supportive care, quality-of-life and survival issues. The journal will also accept case reports dealing with the use of novel technologies, both in the arena of diagnosis and treatment. Supplementary material is welcomed.
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