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一名患有HELLP综合征的女性发生脊髓蛛网膜下腔血肿:病例报告

Spinal subarachnoid hematoma in a woman with HELLP syndrome: a case report.

作者信息

Fujimaki Hisako, Nakazawa Toshiyuki, Ueno Masaki, Imura Takayuki, Saito Wataru, Takahira Naonobu, Takaso Masashi

机构信息

Department of Orthopedic Surgery, Kitasato University School of Medicine, 1-15-1 Kitasato, Sagamihara, Kanagawa, 228-8555, Japan.

出版信息

J Med Case Rep. 2012 Jun 13;6:152. doi: 10.1186/1752-1947-6-152.

Abstract

INTRODUCTION

Subarachnoid hemorrhages of spinal origin are extremely rare during pregnancy. We present the case of a patient with hemolytic anemia, elevated liver enzymes and low platelet count (the so-called HELLP syndrome), a potentially life-threatening complication associated with pre-eclampsia, who presented with an idiopathic spinal subarachnoid hematoma.

CASE PRESENTATION

At 29 gestational weeks, a 35-year-old Japanese woman was diagnosed with HELLP syndrome based on bilateral leg paralysis, diminished sensation and reflexes, and laboratory findings. The pregnancy was immediately brought to an end by Cesarean delivery. Post-operatively, an MRI scan revealed a space-occupying lesion in her thoracic spinal canal. Emergency decompression was followed by total laminectomy. A subarachnoid hematoma, partially extending as far as the ventral side, was removed. After thorough washing and drain placement, the operation was completed with the suturing of artificial dura mater. Eight months post-operatively, her lower extremity sensation had improved to a score of 8 out of 10, but improvements in her muscular strength were limited to slight gains in her toes. MRI scans taken two months post-operatively revealed edematous spinal cord changes within her medulla.

CONCLUSIONS

A subarachnoid hematoma during pregnancy is extremely rare, possibly due to increased coagulability during pregnancy. However, this complication is potentially devastating should a clot compress the spinal cord or cauda equina. While several causes of hematoma have been proposed, we speculate that the factors underlying hemorrhagic diathesis in our case were the decreased platelet count characteristic of HELLP syndrome and vascular fragility due to elevated estrogen levels, in addition to increased abdominal pressure during pregnancy and pressure from the gravid uterus resulting in ruptured vessels around the spinal cord. In cases displaying a progressive lesion and severe neurological signs, prompt decompression is crucial.

摘要

引言

孕期脊髓源性蛛网膜下腔出血极为罕见。我们报告一例患有溶血性贫血、肝酶升高及血小板计数降低(即所谓的HELLP综合征)的患者,这是一种与子痫前期相关的潜在致命并发症,该患者出现了特发性脊髓蛛网膜下腔血肿。

病例介绍

孕29周时,一名35岁的日本女性因双侧腿部麻痹、感觉和反射减退以及实验室检查结果被诊断为HELLP综合征。立即通过剖宫产结束妊娠。术后,MRI扫描显示其胸段椎管内有占位性病变。紧急减压后进行了全椎板切除术。切除了一个蛛网膜下腔血肿,部分血肿延伸至腹侧。彻底冲洗并放置引流管后,用人造硬脑膜缝合完成手术。术后八个月,她下肢的感觉改善至10分制中的8分,但肌肉力量的改善仅限于脚趾略有增强。术后两个月的MRI扫描显示其延髓内脊髓有水肿变化。

结论

孕期蛛网膜下腔血肿极为罕见,可能是由于孕期凝血性增加。然而,如果血凝块压迫脊髓或马尾,这种并发症可能具有毁灭性。虽然已提出血肿的多种病因,但我们推测本例出血素质的潜在因素是HELLP综合征特有的血小板计数降低、雌激素水平升高导致的血管脆性增加,此外还有孕期腹压增加以及妊娠子宫的压力导致脊髓周围血管破裂。对于表现为进行性病变和严重神经体征的病例,及时减压至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2242/3411404/a9a2ca9650b5/1752-1947-6-152-1.jpg

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