Systemic Sarcoidosis Presenting with Headache and Stroke-Like Episodes.

IF 0.7 Q4 IMMUNOLOGY
Case Reports in Immunology Pub Date : 2015-01-01 Epub Date: 2015-09-29 DOI:10.1155/2015/619867
J Campbell, R Kee, D Bhattacharya, P Flynn, M McCarron, A Fulton
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引用次数: 8

Abstract

Sarcoidosis is a multisystem granulomatous disorder. Neurological manifestations as a presenting symptom are relatively rare. A 26-year-old male presented with a five-week history of headache suggestive of raised intracranial pressure. He subsequently developed transient episodes of mild right-sided hemiparesis and numbness. Magnetic resonance imaging (MRI) of brain revealed widespread inflammatory white matter lesions, an ischaemic focus in the left corona radiata, and widespread microhaemorrhages consistent with a more diffuse vasculopathy. Serum angiotensin-converting enzyme (ACE) level was normal. Lumbar puncture revealed an elevated opening pressure (36 cmH2O) and inflammatory cerebrospinal fluid (CSF). Computerised tomography (CT) of chest, abdomen, and pelvis revealed widespread lymphadenopathy and biopsy of axillary lymph nodes revealed the presence of noncaseating granulomata in keeping with systemic sarcoidosis. The patient responded well to corticosteroids. This case highlights the importance of considering sarcoidosis to be a rare but potentially treatable cause of stroke in younger patients.

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系统性结节病表现为头痛和卒中样发作。
结节病是一种多系统肉芽肿性疾病。以神经系统表现为首发症状的病例相对较少。一名26岁男性,有5周的头痛病史,提示颅内压升高。他随后出现短暂的轻度右侧偏瘫和麻木。脑磁共振成像(MRI)显示广泛的炎症性白质病变,左侧放射冠区缺血性病灶,广泛的微出血与弥漫性血管病变一致。血清血管紧张素转换酶(ACE)水平正常。腰椎穿刺显示开口压升高(36 cmH2O)和脑脊液(CSF)炎症。胸部、腹部和骨盆的计算机断层扫描(CT)显示广泛的淋巴结病变,腋窝淋巴结活检显示存在与系统性结节病一致的非肠化肉芽肿。病人对皮质类固醇反应良好。这个病例强调了考虑结节病是一个罕见的,但潜在的治疗原因中风的年轻患者的重要性。
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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来源期刊
CiteScore
1.90
自引率
0.00%
发文量
14
审稿时长
15 weeks
期刊介绍: Case Reports in Immunology is a peer-reviewed, Open Access journal that publishes case reports and case series related to allergies, immunodeficiencies, autoimmune diseases, immune disorders, cancer immunology and transplantation immunology.
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