嗜铬细胞瘤和副神经节瘤胃肠道表现的处理方法。

IF 3 3区 医学 Q2 ENDOCRINOLOGY & METABOLISM
Monica Majumder, Cherie Chiang, Grace Kong, Michael Michael, Nirupa Sachithanandan, Emma Boehm
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引用次数: 0

摘要

目的:控制嗜铬细胞瘤和副神经节瘤(PPGL)患者的胃肠道症状是具有挑战性的,因为许多常用药物存在儿茶酚胺能危机的风险,特别是在功能性肿瘤中。我们回顾了本中心PPGL患者的胃肠道症状管理和结果,并根据文献综述和我们的经验提出了建议。设计、患者、测量:完成了2019年至2024年PPGL患者胃肠道症状管理的单中心回顾性分析。我们对PPGL的胃肠道表现进行了文献回顾。结果:24例PPGL患者接受了放射性核素治疗、化疗、手术或其他内科疾病。18例(75%)有转移性疾病。50例止吐药治疗恶心或呕吐。2例患者出现急性结肠假性梗阻。多巴胺拮抗剂(甲氧氯普胺)和皮质类固醇(地塞米松)分别用于10例和9例患者,其中大多数是α阻断(n = 7)或具有多巴胺能/生化沉默表型(n = 10)。1例去肾上腺素能性PPGL患者在大剂量地塞米松治疗后出现高血压发作。生化阴性/多巴胺能表型或α阻断的患者均未发生止吐相关不良事件。已发表的多巴胺拮抗剂和皮质类固醇引起儿茶酚胺能危机的证据大多局限于病例报告。虽然低风险止吐药(血清素、组胺或神经激动素拮抗剂)是优选的,但我们发现高风险止吐药(地塞米松和甲氧氯普胺)可以谨慎地用于生化阴性/多巴胺能表型的患者或充分阻断的患者。有限的病例报告表明,抗胆碱能药物有利于治疗急性结肠假性梗阻。结论:PPGL患者胃肠道症状的最佳管理应考虑疾病特点,如原发部位、分泌谱、α阻断剂和药物谱。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Approach to the Management of Gastrointestinal Manifestations in Patients With Phaeochromocytoma and Paraganglioma.

Objective: Managing gastrointestinal symptoms in patients with phaeochromocytoma and paraganglioma (PPGL) is challenging due to the risk of catecholaminergic crisis with many commonly prescribed medications, especially in functional tumours. We reviewed gastrointestinal symptom management and outcomes in PPGL patients at our centre and developed recommendations based on a literature review and our experience.

Design, patients, measurement: A single-centre retrospective analysis of the management of gastrointestinal symptoms in patients with PPGL between 2019 and 2024 was completed. A literature review of gastrointestinal manifestations in PPGL was undertaken.

Results: Twenty-four individuals with PPGL admitted for radionuclide therapy, chemotherapy, surgery or other medical illness were included. Eighteen (75%) had metastatic disease. Fifty administration events of antiemetics for nausea or vomiting occurred. Two patients had acute colonic pseudo-obstruction. Dopamine antagonists (metoclopramide) and corticosteroids (dexamethasone) were administered to 10 and 9 patients, respectively, the majority of whom were alpha-blocked (n = 7) or had a dopaminergic/biochemically silent phenotype (n = 10). A patient with noradrenergic PPGL experienced a hypertensive episode following high-dose dexamethasone. No patients with biochemically negative/dopaminergic phenotypes or on alpha blockade experienced an antiemetic-related adverse event. Published evidence of dopamine antagonists and corticosteroids precipitating catecholaminergic crisis was mostly limited to case reports. While low-risk antiemetics (serotonin, histamine or neurokinin antagonists) are preferable, we found higher-risk antiemetics (dexamethasone and metoclopramide) can be cautiously administered in patients with a biochemically negative/dopaminergic phenotype or in those on adequate alpha blockade. Limited case reports demonstrated anti-cholinergic agents were beneficial for the management of acute colonic pseudo-obstruction.

Conclusions: Optimal management of gastrointestinal symptoms in PPGL should consider disease characteristics such as primary location, secretory profile, alpha blockade and medication profile.

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来源期刊
Clinical Endocrinology
Clinical Endocrinology 医学-内分泌学与代谢
CiteScore
6.40
自引率
3.10%
发文量
192
审稿时长
1 months
期刊介绍: Clinical Endocrinology publishes papers and reviews which focus on the clinical aspects of endocrinology, including the clinical application of molecular endocrinology. It does not publish papers relating directly to diabetes care and clinical management. It features reviews, original papers, commentaries, correspondence and Clinical Questions. Clinical Endocrinology is essential reading not only for those engaged in endocrinological research but also for those involved primarily in clinical practice.
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