Unrecognised pheochromocytoma in pregnancy discovered through metoclopramide-triggered hypertensive emergency.

IF 1.8 4区 医学 Blood Pressure Pub Date : 2021-10-01 Epub Date: 2021-06-26 DOI:10.1080/08037051.2021.1945428
Aurelio Negro, Ignazio Verzicco, Stefano Tedeschi, Rosaria Santi, Barbara Palladini, Anna Calvi, Alessandro Giunta, Davide Cunzi, Pietro Coghi, Riccardo Volpi, Aderville Cabassi
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引用次数: 6

Abstract

Purpose: Pheochromocytoma, a catecholamine-secreting tumour leading to neurological and cardiovascular life-threatening conditions through hypertension crisis, occurs in 0.1-0.5% of hypertensive patients, but it is extremely rare in pregnancy (0.0018-0.006%). Some classes of drugs, even commonly used in pregnancy, can trigger catecholamine secretion, precipitating the clinical situation.

Materials and methods and results: We report a 33-year-old woman, gravida 2 para 1, with previous mild hypertension, was admitted to the emergency room, at 28 2/7 weeks of gestation due to headache, tachycardia and severe arterial hypertension (220/120 mm Hg) triggered by the antiemetic metoclopramide used for a week because of nausea. In the emergency room, a paradoxical rise in blood pressure followed intravenous labetalol infusion was observed. Both metoclopramide and labetalol-triggered hypertensive crisis raised the suspicion of an undiagnosed pheochromocytoma. Diagnostic work-up showed elevated normetanephrine urinary excretion ​​and a right adrenal pheochromocytoma by abdominal magnetic resonance imaging. Oral alpha-1 and beta-1-adrenergic antagonist and calcium-channel blocker were started. At 33-weeks of gestation, she underwent a caesarean section giving birth to a female child. Seven weeks later she underwent a video-laparoscopic right adrenalectomy which normalised her blood pressure.

Conclusions: Both metoclopramide, a selective dopamine type-2 receptor antagonist and partial agonist of 5-hydroxytryptamine 4 receptor, and labetalol, a non-selective β-adrenoreceptor-blocker with weak α1-adrenergic antagonism, exacerbated an acute hypertensive crisis revealing an unrecognised pheochromocytoma in a pregnant patient. Careful attention to potential drug-triggered catecholamine crises and especially early recognition of pheochromocytomas, are mandatory in hypertensive pregnant women. A missed or delayed diagnosis could result in catastrophic results affecting foetal and maternal outcomes.

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通过甲氧氯普胺引发的高血压急诊发现妊娠期未被识别的嗜铬细胞瘤。
目的:嗜铬细胞瘤是一种分泌儿茶酚胺的肿瘤,在高血压患者中发生率为0.1-0.5%,可通过高血压危象导致危及神经系统和心血管的疾病,但在妊娠期极为罕见(0.0018-0.006%)。某些类别的药物,即使是孕期常用的药物,也会引发儿茶酚胺分泌,诱发临床症状。材料、方法和结果:我们报告了一名33岁妇女,妊娠2期1,既往轻度高血压,于妊娠28 2/7周因头痛、心动过速和严重动脉高血压(220/120 mm Hg)而入院急诊室,该患者因恶心而使用止吐药甲氧氯普胺一周。在急诊室,观察到静脉输注拉贝他洛尔后血压反常升高。甲氧氯普胺和拉贝洛尔引发的高血压危象都引起了对未确诊的嗜铬细胞瘤的怀疑。诊断检查显示尿中去甲肾上腺素分泌升高,腹部磁共振成像显示右侧肾上腺嗜铬细胞瘤。开始口服α -1和β -1肾上腺素能拮抗剂和钙通道阻滞剂。在怀孕33周时,她接受了剖腹产手术,生下了一个女婴。七周后,她接受了视频腹腔镜右肾上腺切除术,血压恢复正常。结论:甲氧氯普胺(选择性多巴胺2型受体拮抗剂和5-羟色胺4受体的部分激动剂)和拉贝他洛尔(非选择性β-肾上腺素受体阻滞剂,具有弱α - 1肾上腺素能拮抗作用)加重了妊娠患者的急性高血压危象,显示出未被识别的嗜铬细胞瘤。高血压孕妇必须注意潜在的药物引发的儿茶酚胺危机,特别是早期识别嗜铬细胞瘤。错过或延迟诊断可能导致影响胎儿和产妇结局的灾难性后果。
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来源期刊
Blood Pressure
Blood Pressure Medicine-Cardiology and Cardiovascular Medicine
CiteScore
3.20
自引率
5.60%
发文量
41
期刊介绍: For outstanding coverage of the latest advances in hypertension research, turn to Blood Pressure, a primary source for authoritative and timely information on all aspects of hypertension research and management. Features include: • Physiology and pathophysiology of blood pressure regulation • Primary and secondary hypertension • Cerebrovascular and cardiovascular complications of hypertension • Detection, treatment and follow-up of hypertension • Non pharmacological and pharmacological management • Large outcome trials in hypertension.
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