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两名α-1抗胰蛋白酶缺乏症患者成功进行脾肾分流术和脾切除术。

Successful spleno-renal shunt and splenectomy in two patients with alpha-1-antitrypsin deficiency.

作者信息

Sotos J F, Cutler E A, Romshe C A, Clatworthy H W

出版信息

J Pediatr Surg. 1981 Feb;16(1):12-6. doi: 10.1016/s0022-3468(81)80107-8.

Abstract

Recent evidence suggests that the cirrhosis of alpha-1-antitrypsin deficiency is not invariably fatal as it was previously thought. Portal hypertension is often the major determinant of survival. The few reports of porta-systemic venous anastomosis in this disorder have shown poor results or uncertain outcome. Thus, doubts exist as to whether porta-systemic shunts should be performed in alpha-1-antitrypsin deficiency. Two patients with alpha-1-antitrypsin deficiency (PiZZ) and associated portal hypertension, cirrhosis, and hypersplenism underwent splenorenal shunt and splenectomy 8 yr ago, and both have done well. One of the patients has chronic severe headaches, diarrhea, exudative enteropathy, sinusitis, and hematuria, all uncommon in alpha-1-antitrypsin deficiency but possibly related to the antienzyme deficiency. She also has a higher trypsin inhibitory capacity than is generally reported in ZZ individuals. Based on the experience with these 2 patients, it appears that alpha-1-antitrypsin deficiency with cirrhosis is not a valid contraindication to the performance of a portasystemic shunt.

摘要

最近的证据表明,α1抗胰蛋白酶缺乏症导致的肝硬化并非如之前所认为的那样必然致命。门静脉高压常常是生存的主要决定因素。关于这种病症的门体静脉吻合术的少数报告显示效果不佳或预后不确定。因此,对于α1抗胰蛋白酶缺乏症患者是否应进行门体分流术存在疑问。两名患有α1抗胰蛋白酶缺乏症(PiZZ型)并伴有门静脉高压、肝硬化和脾功能亢进的患者在8年前接受了脾肾分流术和脾切除术,两人情况都良好。其中一名患者患有慢性严重头痛、腹泻、渗出性肠病、鼻窦炎和血尿,这些在α1抗胰蛋白酶缺乏症中都不常见,但可能与抗酶缺乏有关。她的胰蛋白酶抑制能力也比一般ZZ个体报告的要高。基于这两名患者的经验,看来伴有肝硬化的α1抗胰蛋白酶缺乏症并非进行门体分流术的有效禁忌证。

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