首页 | 本学科首页   官方微博 | 高级检索  
     


Subacute myelopathy revealing systemic sarcoidosis
Authors:Boulaajaj F Z  Rafai M A  El Otmani H  El Moutawakkil B  Hakim K  Fadel H  Slassi I
Affiliation:Service de Neurologie--Explorations Fonctionnelles, CHU Ibn Rochd, Quartier des H?pitaux, Casablanca, Maroc. mo.mi2@caramail.com
Abstract:
INTRODUCTION: The spinal localization is rare for neurosarcoidosis (0.43 percent of cases) but can be the inaugural manifestation of the disease. We report two cases of spinal neurosarcoidosis in a 57-year-old man and a 43-year*old woman with uneventful past medical histories. Both presented progressive myelopathic features. METHODS: Magnetic resonance imaging (MRI) of the spine demonstrated intramedullary lesions, dorsal in the first case, and cervical in the second case. Serum angiotensin converting enzyme was elevated. Radiographs of the chest revealed bilateral symmetric hilar mediastinal lymphadenopathy in the first patient, and bronchial biopsy demonstrated non caseating granulomas. In the second patient the diagnosis was made on pathological examination of a minor salivary gland biopsy. RESULTS: The patients received corticosteroid therapy with good response in the second patient. CONCLUSION: The diagnosis of intramedullary sarcoidosis is difficult without a previous diagnosis of systemic sarcoidosis or other apparent symptom(s). Extraneurologic biopsies may be suggestive. We reviewed the literature on the diagnosis and treatment of intramedullary sarcoidosis.
Keywords:Sarcoïdose   Neurosarcoïdose   Myélopathies   Granulome   Épithélio-giganto-cellulaire sans nécrose caséeuse
本文献已被 ScienceDirect PubMed 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号