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双侧头皮坏死是巨细胞动脉炎一种罕见但严重的并发症。

Bilateral scalp necrosis as a rare but devastating complication of giant cell arteritis.

作者信息

Akram Q, Knight S, Saravanan R

机构信息

Macclesfield District General Hospital, Victoria Road, Macclesfield, SK10 3BL, UK,

出版信息

Clin Rheumatol. 2015 Jan;34(1):185-7. doi: 10.1007/s10067-014-2792-y. Epub 2014 Oct 17.

Abstract

Giant cell arteritis (GCA) is a medium to large vessel vasculitis of unknown aetiology. Commonly, it affects the temporal arteries and is known as temporal arteritis. It has an association with polymyalgia rheumatica and can result in severe complications such as loss of vision and rarely scalp necrosis. There are approximately 100 cases of scalp necrosis in patients with GCA published in the literature to date. We report a case of a man who presented with a 4-week history of bilateral scalp necrosis associated with headache, jaw claudication, temporal artery tenderness, and raised inflammatory markers. He did not have any visual loss. A diagnosis of GCA was made and he was started on high-dose steroids immediately. The scalp lesions did improve and his symptoms resolved without any visual loss but, sadly he died due to severe sepsis. This case report is important as it describes a rare but severe complication of a common large vessel vasculitis seen by both primary care physicians and rheumatologists. Prompt recognition and early treatment by the physician are crucial to the patient to prevent visual loss or a fatal stroke. It also highlights complications associated with steroids which are the mainstay of treatment for this condition.

摘要

巨细胞动脉炎(GCA)是一种病因不明的中到大血管血管炎。通常,它会影响颞动脉,被称为颞动脉炎。它与风湿性多肌痛有关,可导致严重并发症,如视力丧失,很少见的头皮坏死。迄今为止,文献中报道的GCA患者中约有100例出现头皮坏死。我们报告一例男性患者,有4周双侧头皮坏死病史,伴有头痛、颌部间歇性运动障碍、颞动脉压痛及炎症标志物升高。他没有任何视力丧失。诊断为GCA后,立即开始给予大剂量类固醇治疗。头皮病变确实有所改善,他的症状得到缓解,没有出现任何视力丧失,但遗憾的是,他因严重脓毒症死亡。本病例报告很重要,因为它描述了基层医疗医生和风湿病学家都能见到的一种常见大血管血管炎的罕见但严重的并发症。医生的及时识别和早期治疗对患者预防视力丧失或致命性中风至关重要。它还突出了与类固醇相关的并发症,而类固醇是这种疾病治疗的主要手段。

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