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首页> 外文期刊>Transplantation: Official Journal of the Transplantation Society >Reappraisal of the Role of Portacaval Shunting in the Growth of Patients With Glycogen Storage Disease Type I in the Era of Liver Transplantation
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Reappraisal of the Role of Portacaval Shunting in the Growth of Patients With Glycogen Storage Disease Type I in the Era of Liver Transplantation

机译:对肝移植时代门腔分流在糖原贮积病I型患者生长中的作用的重新评估

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Background. Instead of dietary modification, surgical management is considered for correcting growth retardation, poor metabolic control, and hepatocellular adenoma (HCA) in glycogen storage disease (GSD) type I. Methods. The records of 55 GSD type I patients were retrospectively reviewed. Thirty-two patients underwent only dietarymanagement (group D) and 23 underwent surgical management (group S). In group S, 17 underwent portacaval shunting (PCS), 13 underwent liver transplantation (LT; 7 underwent both PCS and LT). Height-for-age and body mass index-for-age Z-scores based on World Health Organization data were used to compare growth patterns before and after surgery. Changes in metabolic abnormalities and HCA after operation were also investigated. Results. Height-for-age Z-scores for group S were higher by an average of 0.377 compared to that for group D. Metabolic abnormalities often disappeared after LT but improved partially after PCS. De novo HCA was detected in 4 patients (13%) from group D, 12 (100%) who underwent PCS, and none who underwent LT. One case of hepatocellular carcinoma and one of hemorrhage from a HCA were noted in group D. Two cases of hepatocellular carcinoma, 2 of hemorrhage, and 1 of necrosis were noted after PCS. Conclusions. Surgery yielded greater growth improvement than dietary management. However, after PCS, metabolic abnormalities remained unresolved, and the de novo HCA rate was high. Portacaval shunting can be used to improve growth in GSD type I patients when LT is not possible, but close observation for metabolic abnormalities and HCA is essential.
机译:背景。代替饮食调整,考虑通过外科手术来纠正I型糖原贮积病(GSD)中的生长迟缓,代谢控制不良和肝细胞腺瘤(HCA)。回顾性分析55例GSD I型患者的病历。仅对饮食进行饮食管理的有32例(D组),而对外科治疗的23例(S组)。在S组中,有17例行门腔分流(PCS),有13例行肝移植(LT; 7例行PCS和LT)。基于世界卫生组织数据的年龄高度和年龄体重Z分数用于比较手术前后的生长方式。还调查了术后代谢异常和HCA的变化。结果。与D组相比,S组的平均身高Z值平均高0.377。代谢异常通常在LT后消失,而在PCS后有所改善。 D组中有4例(13%)患者进行了从头HCA检测,PCS患者中有12例患者(100%)被检测出,而LT患者中没有检测到。 D组注意到1例肝细胞癌和1例HCA出血。PCS后发现2例肝细胞癌,2例出血和1例坏死。结论。外科手术比饮食管理产生了更大的增长改善。然而,PCS后,代谢异常仍未解决,并且从头HCA发生率很高。当不可能进行LT时,可使用门腔分流术来改善I型GSD患者的生长,但必须密切观察代谢异常和HCA。

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