帕西瑞奥肽能迅速缓解肢端肥大症成人患者的顽固性头痛

JCEM case reports Pub Date : 2024-08-09 eCollection Date: 2024-08-01 DOI:10.1210/jcemcr/luae142
Zeinab Dabbous, Zaina Rohani, Abeer Kaled Abdalrubb, Yaman Alkailani, Rosario Pivonello, Tarik Elhadd
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引用次数: 0

摘要

肢端肥大症是一种由 GH 分泌过多引起的慢性内分泌失调症。除了生理症状外,它还经常伴有使人衰弱的头痛。虽然存在有效的治疗方案,但要完全控制症状和控制病情仍然具有挑战性。本病例报告记录了一名 38 岁男性于 2013 年被诊断为肢端肥大症的临床历程。尽管之前采取了包括手术和第一代体生长激素类似物治疗在内的干预措施,但严重的频繁头痛仍然存在。在改用帕司瑞肽治疗后,患者报告头痛迅速完全缓解,IGF-1水平也在一个月内恢复正常。该报告强调了肢端肥大症治疗所面临的挑战,并证实了帕西瑞肽对治疗耐药头痛患者的潜在作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Rapid Resolution of Recalcitrant Headache With Pasireotide in an Adult Patient With Acromegaly.

Acromegaly is a chronic hormonal disorder caused by excessive GH secretion. In addition to physiological symptoms, it is often accompanied by debilitating headaches. Although effective treatment options exist, achieving complete symptom control and disease management can still be challenging. This case report chronicles the clinical journey of a 38-year-old male diagnosed with acromegaly in 2013. Despite prior interventions, including surgery and treatment with first-generation somatostatin analogues, severe frequent headaches persisted. Following a switch to pasireotide, the patient reported rapid and complete resolution of headaches and normalization of IGF-1 levels within a month of the treatment switch. This report underscores the challenges in acromegaly management and confirms the potential utility of pasireotide for patients suffering from treatment-resistant headache.

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