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小儿血液病脾切除术后门静脉系统血栓形成

Thrombosis of the portal venous system after splenectomy for pediatric hematologic disease.

作者信息

Skarsgard E, Doski J, Jaksic T, Wesson D, Shandling B, Ein S, Babyn P, Heiss K, Hu X

机构信息

Department of Surgery, Hospital For Sick Children, Toronto, Ontario, Canada.

出版信息

J Pediatr Surg. 1993 Sep;28(9):1109-12. doi: 10.1016/0022-3468(93)90141-7.

Abstract

Splenic, portal, or mesenteric venous thrombosis after splenectomy for hematologic disease has not been reported in the pediatric literature. It is a rare complication associated with significant morbidity and mortality in adult reports. Between 1981 and 1991, 3 patients (13-year-old boy with hereditary elliptocytosis [HE], 13-year-old boy with thalassemia intermedia [TI], and 18-year-old girl with idiopathic thrombocytopenic purpura [ITP]) presented with abdominal pain, nausea, with or without fever, at 4, 11, and 13 days postsplenectomy, respectively. Abdominal Doppler ultrasound (US) and/or computed tomography (CT) showed: (1) an intraluminal filling defect with partial obstruction to flow in the right branch of the portal vein with the remaining vessels patent (HE); (2) splenic vein thrombosis with complete occlusion of the main portal vein and proximal superior mesenteric vein (TI); and (3) complete thrombosis of the splenic vein, proximal superior mesenteric vein and portal vein (including central radicles), with retrogastric collateralization (ITP). Subsequent imaging showed either complete resolution of vascular obstruction on no treatment (patient 1), or portal venous cavernomatous transformation with hepatofugal flow after 6 months of systemic anticoagulation (patients 2 and 3), and all 3 patients are currently asymptomatic. Postoperative sonographic evaluation of a consecutive series of pediatric splenectomies for hematologic disease (n = 16), was performed at a median of 51 days (range, 3 to 124). This demonstrated one case of asymptomatic left portal venous thrombosis with subsequent recanalization in the absence of treatment.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

小儿血液系统疾病脾切除术后发生脾静脉、门静脉或肠系膜静脉血栓形成的情况在儿科文献中尚无报道。在成人报告中,这是一种罕见的并发症,可导致显著的发病率和死亡率。1981年至1991年间,3例患者(1例13岁患遗传性椭圆形红细胞增多症[HE]的男孩、1例13岁患中间型地中海贫血[TI]的男孩和1例18岁患特发性血小板减少性紫癜[ITP]的女孩)分别在脾切除术后4天、11天和13天出现腹痛、恶心,伴或不伴有发热。腹部多普勒超声(US)和/或计算机断层扫描(CT)显示:(1)门静脉右支腔内充盈缺损伴血流部分受阻,其余血管通畅(HE);(2)脾静脉血栓形成,主门静脉和肠系膜上静脉近端完全闭塞(TI);(3)脾静脉、肠系膜上静脉近端和门静脉(包括中央分支)完全血栓形成,胃后有侧支循环(ITP)。后续影像学检查显示,1例未经治疗血管阻塞完全消退(患者1),另2例(患者2和3)经6个月全身抗凝治疗后门静脉海绵样变性伴肝外血流,目前3例患者均无症状。对一系列连续的因血液系统疾病行脾切除术的小儿患者(n = 16)进行术后超声评估,评估时间中位数为51天(范围3至124天)。结果显示1例无症状的左门静脉血栓形成,未经治疗随后再通。(摘要截短于250字)

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