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III型戈谢病部分脾切除术后因疾病进展导致的致命性出血。

Fatal hemorrhage caused by disease progression after partial splenectomy for type III Gaucher's disease.

作者信息

Holcomb G W, Greene H L

机构信息

Department of Pediatric Surgery, Vanderbilt University Medical Center, Nashville, TN.

出版信息

J Pediatr Surg. 1993 Dec;28(12):1572-4. doi: 10.1016/0022-3468(93)90101-p.

Abstract

An 18-month-old boy with Gaucher's disease, massive hepatosplenomegaly, and hypersplenism underwent partial (85%) splenectomy and recovered without complication. During the next 4 months, his residual splenic segment showed progressive enlargement from 2 to 6 cm below the left costal margin. By this time, genetic typing had indicated central nervous system involvement (type III). A compatible donor was not available for bone marrow transplantation. Complete splenectomy was not recommended despite continued enlargement of the organ into the pelvis and across the abdominal midline by 7 1/2 months postoperatively. The next week he presented to the emergency room in shock with an hematocrit of 6% and a platelet count of 18,000/mm3. During emergency surgery, massive intraabdominal hemorrhage was noted from a splenic rupture on the inferior pole that was opposite the site of prior division. He died in the operating room during attempted splenectomy. This is a report of fatal outcome after partial splenectomy for type III Gaucher's disease. Patients with subacute neuronopathic disease may not be candidates for subtotal splenectomy.

摘要

一名患有戈谢病、巨脾症和脾功能亢进的18个月大男孩接受了部分(85%)脾切除术,术后恢复良好,未出现并发症。在接下来的4个月里,他残余的脾段从左肋缘下2厘米逐渐增大至6厘米。此时,基因分型显示有中枢神经系统受累(III型)。没有合适的骨髓移植供体。尽管术后7个半月脾脏持续增大并延伸至盆腔及跨越腹部中线,但仍不建议进行全脾切除术。下周,他因休克被送往急诊室,血细胞比容为6%,血小板计数为18,000/mm³。在急诊手术中,发现脾脏下极一处与之前手术部位相对的破裂处有大量腹腔内出血。在试图进行脾切除术时,他死于手术室。这是一篇关于III型戈谢病行部分脾切除术后致命结局的报告。患有亚急性神经病变型疾病的患者可能不适合行次全脾切除术。

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