Acute Brachial Radiculoplexopathy and Giant Cell Arteritis

被引:7
作者
Duval, Fanny [1 ]
Lacoste, Idoia [1 ]
Galli, Gael [1 ]
Chaumont, Hugo [1 ]
Sole, Guilhem [1 ]
Leger, Francois [3 ]
Damon-Perriere, Nathalie [2 ]
Rouanet, Marie [2 ]
Le Masson, Gwendal [1 ]
Mathis, Stephane [1 ]
机构
[1] CHU Bordeaux, Nerve Muscle Unit, Dept Neurol, Grp Hosp Pellegrin, Pl Amelie Raba Leon, F-33000 Bordeaux, France
[2] CHU Bordeaux, Dept Clin Neurophysiol, Grp Hosp Pellegrin, Pl Amelie Raba Leon, Bordeaux, France
[3] CHU Bordeaux, Dept Pathol, Grp Hosp Pellegrin, Pl Amelie Raba Leon, Bordeaux, France
关键词
Giant cell arteritis; Horton; radiculopathy; plexopathy; C5-C6; PERIPHERAL NERVOUS-SYSTEM; CERVICAL RADICULOPATHY; POLYMYALGIA-RHEUMATICA; TEMPORAL ARTERITIS; PRESENTING SYMPTOM; INVOLVEMENT; PLEXOPATHY; CLASSIFICATION; MANIFESTATION; RARE;
D O I
10.1097/NRL.0000000000000162
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Introduction:Giant cell arteritis (GCA), a vasculitis involving large-sized and medium-sized vessels (which most commonly involves temporal arteries), is easily recognized in older patients presenting with headache, scalp tenderness, and raised inflammatory markers. Neurological complications (either central or peripheral) are classically described in GCA.Case Report:We report the case of an 85-year-old woman with bilateral acute brachial radiculoplexopathy, a rare neurological complication of GCA. She also presented right oculomotor palsy (with ptosis) and raised inflammatory markers, but she did not complain of the other classic cranial symptoms of the disease. We compare this case with 16 similar cases reported in the medical literature.Conclusions:In assessing a patient over 50 years of age with unexplained (unilateral or bilateral) brachial radiculoplexopathy (especially if C5-C6 nerve roots are affected) and elevated inflammatory markers, we would recommend specific enquiries with regard to the manifestations of GCA. The purpose is to reduce the risk of missing the wider spectrum of this condition and minimize the subsequent risk for disability of this treatable disease.
引用
收藏
页码:23 / 28
页数:6
相关论文
共 32 条
[1]  
Andrzejczak A., 2001, ACTA CLIN, V1, P111
[2]   Diagnostic performance of 18F-fluorodeoxyglucose positron emission tomography in giant cell arteritis: a systematic review and meta-analysis [J].
Besson, Florent L. ;
Parienti, Jean-Jacques ;
Bienvenu, Boris ;
Prior, John O. ;
Costo, Sylvie ;
Bouvard, Gerard ;
Agostini, Denis .
EUROPEAN JOURNAL OF NUCLEAR MEDICINE AND MOLECULAR IMAGING, 2011, 38 (09) :1764-1772
[3]   Giant cell arteritis revealed by brachial C5 plexopathy [J].
Blaise, S ;
Liozon, E ;
Nadalon, S ;
Vidal, E .
REVUE DE MEDECINE INTERNE, 2005, 26 (07) :578-582
[4]   Giant cell arteritis: A review of classification, pathophysiology, geoepidemiology and treatment [J].
Borchers, Andrea T. ;
Gershwin, M. Eric .
AUTOIMMUNITY REVIEWS, 2012, 11 (6-7) :A544-A554
[5]   STEROID-RESPONSIVE ELECTROMYOGRAPHIC ABNORMALITIES IN POLYMYALGIA RHEUMATICA [J].
BROMBERG, MB ;
DONOFRIO, PD ;
SEGAL, BM .
MUSCLE & NERVE, 1990, 13 (02) :138-141
[6]  
CALAMIA KT, 1980, CLIN RHEUM DIS, V6, P389
[7]   NEUROLOGIC DISEASE IN BIOPSY-PROVEN GIANT-CELL (TEMPORAL) ARTERITIS [J].
CASELLI, RJ ;
HUNDER, GG ;
WHISNANT, JP .
NEUROLOGY, 1988, 38 (03) :352-359
[8]  
Chowdhry IA, 2002, J RHEUMATOL, V29, P2653
[9]   Giant-cell arteritis without cranial manifestations: Working diagnosis of a distinct disease pattern [J].
de Boysson, Hubert ;
Lambert, Marc ;
Liozon, Eric ;
Boutemy, Jonathan ;
Maigne, Gwenola ;
Ollivier, Yann ;
Ly, Kim ;
Manrique, Alain ;
Bienvenu, Boris ;
Aouba, Achille .
MEDICINE, 2016, 95 (26)
[10]   RECURRENT BRACHIAL-PLEXUS NEUROPATHY AND GIANT-CELL ARTERITIS [J].
DIERCKX, RA ;
EBINGER, G ;
HERREGODTS, P ;
MICHOTTE, A ;
CARLY, B ;
SCHMEDDING, E ;
MAILLET, B .
CLINICAL NEUROLOGY AND NEUROSURGERY, 1990, 92 (01) :71-74