Isolated neurosarcoidosis presenting as headache and spinal cord lesions mimicking central nervous system metastases

被引:22
作者
Tsao, Chang-Yong [1 ]
Lo, Warren D.
Rusin, Jerome A.
Henwood, Maria J.
Boue, Daniel R.
机构
[1] Ohio State Univ, Dept Pediat & Neurol, Columbus, OH 43210 USA
[2] Ohio State Univ, Dept Radiol, Columbus, OH 43210 USA
[3] Ohio State Univ, Dept Pediat & Endocrinol, Columbus, OH 43210 USA
[4] Ohio State Univ, Dept Pathol, Columbus, OH 43210 USA
关键词
sarcoidosis; neurosarcoidosis; central nervous system metastases; headache;
D O I
10.1016/j.braindev.2006.12.011
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Sarcoidosis is uncommon in children. Although isolated neurosarcoidosis has been seen in 15% adults with sarcoidosis, pediatric neurosarcoidosis is rarely reported. Neurosarcoidosis may present with cranial neuropathy, including facial palsy, optic nerve or other cranial nerve involvement, peripheral neuropathy, or manifestations of the central nervous system affecting the hypothalamus, pituitary gland, cerebral cortex, cerebellum, meninges, and spinal cord. The useful diagnostic investigations include magnetic resonance imaging of the brain and spinal cord, cerebrospinal fluid studies, brain and meningeal biopsy if feasible, chest radiography to reveal sarcoidosis, angiotensin-converting enzyme level in the serum or cerebrospinal fluid, and Kveim test when available. We herein report a case of isolated brain biopsy-confirmed neurosarcoidosis in a 17-year-old boy presenting with severe unilateral headache and multiple brain and spinal cord MRI lesions mimicking central nervous system metastases. (c) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:514 / 518
页数:5
相关论文
共 21 条
[1]   Neurosarcoid presents differently in children than in adults [J].
Baumann, RJ ;
Robertson, WC .
PEDIATRICS, 2003, 112 (06) :E480-E486
[2]  
Braido F, 2005, SARCOIDOSIS VASC DIF, V22, P75
[3]   NEUROSARCOIDOSIS - SIGNS, COURSE AND TREATMENT IN 35 CONFIRMED CASES [J].
CHAPELON, C ;
ZIZA, JM ;
PIETTE, JC ;
LEVY, Y ;
RAGUIN, G ;
WECHSLER, B ;
BITKER, MO ;
BLETRY, O ;
LAPLANE, D ;
BOUSSER, MG ;
GODEAU, P .
MEDICINE, 1990, 69 (05) :261-276
[4]   Long-term follow-up of neurosarcoidosis [J].
Ferriby, D ;
de Seze, J ;
Stojkovic, T ;
Hachulla, E ;
Wallaert, B ;
Destée, S ;
Hatron, PY ;
Vermersch, P .
NEUROLOGY, 2001, 57 (05) :927-929
[5]   INCREASED HELPER-SUPPRESSOR LYMPHOCYTE-T RATIO IN THE CEREBROSPINAL-FLUID OF A PATIENT WITH NEUROSARCOIDOSIS [J].
JUOZEVICIUS, JL ;
RYNES, RI .
ANNALS OF INTERNAL MEDICINE, 1986, 104 (06) :807-808
[6]   PROGNOSIS OF SARCOIDOSIS IN CHILDREN [J].
KENDIG, EL ;
BRUMMER, DL .
CHEST, 1976, 70 (03) :351-353
[7]   The pitfall of silent neurosarcoidosis [J].
Koné-Paut, I ;
Portas, M ;
Wechsler, B ;
Girard, N ;
Raybaud, C .
PEDIATRIC NEUROLOGY, 1999, 20 (03) :215-218
[8]   Central diabetes insipidus as the first manifestation of neurosarcoidosis in a 10-year-old girl [J].
Konrad, D ;
Gartenmann, M ;
Martin, E ;
Schoenle, EJ .
HORMONE RESEARCH, 2000, 54 (02) :98-100
[9]  
Leiba H, 1996, J NEURO-OPHTHALMOL, V16, P269
[10]  
LI CY, 1992, ACTA CYTOL, V36, P963