Amoah G B
Department of Medicine and Therapetutics, University of Ghana Medical School, Accra, Ghana.
East Afr Med J. 1996 Sep;73(9):623-4.
Landry-Guillain-Barre-Strohl Syndrome (LGBS) is a rare occurrence in pregnancy with only 38 previously reported cases in the literature. A case of a 26 year old Ghanaian woman who presented at thirty weeks gestation with limb weakness, facial diplegia, dysarthria, dysphagia and CSF cytoalbuminic dissociation and who made complete recovery before delivery of a normal full term baby is described. This is the thirty ninth reported case of LGBS in pregnancy in the literature and the first reported case from Black Africa. It is the third reported case of full recovery before delivery. The aetiology, diagnosis and management of LGBS is briefly reviewed.
兰德里-古兰-巴雷-施特罗尔综合征(LGBS)在孕期较为罕见,文献中此前仅报道过38例。本文描述了一名26岁的加纳女性病例,该患者在妊娠30周时出现肢体无力、双侧面瘫、构音障碍、吞咽困难以及脑脊液蛋白细胞分离现象,并在分娩一名正常足月婴儿前完全康复。这是文献中报道的第39例孕期LGBS病例,也是来自黑非洲地区的首例报道病例。这是第3例报道的在分娩前完全康复的病例。本文简要回顾了LGBS的病因、诊断及治疗。