The Curious Case of Confounding Headaches.

Case Reports in Rheumatology Pub Date : 2025-09-27 eCollection Date: 2025-01-01 DOI:10.1155/crrh/2146010
Ram Chandra Khatri Chhetri, Hemanta Paudel, Viswaja Kaja, Jahanzeb Saeed, Jane Nwaonu, Adegbenga Bankole
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Abstract

Giant cell arteritis is the most common primary systemic vasculitis among individuals over 50 years of age. It primarily affects large- and medium-size arteries and is not mediated by antibodies. One of the most recognizable and important symptoms of the disease is headache. The presence of headaches, along with other common cranial manifestations such as vision loss, jaw claudication, and scalp tenderness in the temporal arteries, can assist in diagnosing the condition. We present a complex case involving a 76-year-old male with prolonged headaches, a pituitary macroadenoma, and vestibular schwannoma. Initially, his headaches were attributed to his existing intracranial lesions; however, his symptoms continued to evolve. He continued to have headaches of varying intensity over 2 years, and subsequently developed diffuse scalp tenderness, visual disturbances, and tongue claudication. Input from various medical specialties expanded the differential diagnosis and raised the possibility of giant cell arteritis (GCA). Although the temporal artery biopsy did not reveal the classic giant cells typically associated with the condition, it supported the clinical diagnosis of GCA. Appropriate treatment with high-dose corticosteroids and anti-Interleukin 6 therapy resulted in the rapid resolution of his symptoms. This case emphasizes the importance of recognizing different types of headaches, maintaining a broad differential diagnosis, and thoroughly evaluating all clinical symptoms for timely diagnosis and treatment. It also highlights the significance of a multidisciplinary approach to ensure prompt diagnosis and to prevent irreversible complications, such as permanent vision loss.

混淆性头痛的奇怪案例。
巨细胞动脉炎是50岁以上人群中最常见的原发性系统性血管炎。它主要影响大、中型动脉,并不是由抗体介导的。这种疾病最明显和最重要的症状之一是头痛。头痛的出现,以及其他常见的脑部表现,如视力下降、下颌跛行和颞动脉头皮压痛,可以帮助诊断这种疾病。我们报告一个复杂的病例,涉及一位76岁的男性长期头痛,垂体大腺瘤和前庭神经鞘瘤。最初,他的头痛归因于他现有的颅内病变;然而,他的症状继续恶化。他持续有不同程度的头痛超过2年,随后出现弥漫性头皮压痛、视觉障碍和舌头跛行。来自不同医学专业的意见扩大了鉴别诊断,并提高了巨细胞动脉炎(GCA)的可能性。虽然颞动脉活检未发现与该病相关的典型巨细胞,但它支持GCA的临床诊断。适当的高剂量皮质类固醇和抗白细胞介素6治疗使他的症状迅速缓解。本病例强调了识别不同类型头痛的重要性,保持广泛的鉴别诊断,并彻底评估所有临床症状,以便及时诊断和治疗。它还强调了多学科方法的重要性,以确保及时诊断和预防不可逆转的并发症,如永久性视力丧失。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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审稿时长
12 weeks
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