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儿童淋巴瘤继发梗阻性黄疸

Obstructive jaundice secondary to lymphoma in childhood.

作者信息

Pietsch J B, Shankar S, Ford C, Johnson J E

机构信息

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

出版信息

J Pediatr Surg. 2001 Dec;36(12):1792-5. doi: 10.1053/jpsu.2001.28840.

Abstract

In children, biliary obstruction secondary to lymphoma is rare. Previous reports in adults and children suggest that these lymphomas are associated with a poor prognosis. The authors reviewed the medical records and imaging studies of 4 children treated for pancreaticobiliary lymphoma at our children's hospital over the past 10 years. All 4 presented with jaundice. Abdominal ultrasound scan and computed tomography (CT) scans were helpful in defining the anatomy of the obstruction. In the cases of involvement of the porta hepatis, the diagnosis was made by biopsy. In one child a mass was in the head of the pancreas, and evaluation of frozen section biopsy results were not diagnostic for lymphoma, and a major resection was performed. All the lymphomas were of nonHodgkin's B-cell type and one was a Burkitt's lymphoma. All responded promptly to chemotherapy. One child had a testicular relapse and currently is receiving additional therapy. Pancreaticobiliary lymphomas are an unusual cause of obstructive jaundice in children. Biopsy alone without resection or biliary drainage is recommended surgical therapy. Long-term survival rate in children with this disorder appears to be more promising than previously reported. J Pediatr Surg 36:1792-1795.

摘要

在儿童中,继发于淋巴瘤的胆道梗阻较为罕见。既往针对成人和儿童的报道表明,这些淋巴瘤预后较差。作者回顾了过去10年在我院儿童医院接受胰胆淋巴瘤治疗的4例儿童的病历和影像学检查。所有4例均表现为黄疸。腹部超声扫描和计算机断层扫描(CT)有助于明确梗阻的解剖结构。对于肝门受累的病例,通过活检做出诊断。在1例儿童中,肿块位于胰头,冰冻切片活检结果不能确诊为淋巴瘤,遂进行了大手术切除。所有淋巴瘤均为非霍奇金B细胞型,其中1例为伯基特淋巴瘤。所有患儿对化疗均迅速起效。1例儿童出现睾丸复发,目前正在接受进一步治疗。胰胆淋巴瘤是儿童梗阻性黄疸的罕见病因。建议仅行活检,无需切除或胆道引流,这是手术治疗方法。患有这种疾病的儿童的长期生存率似乎比之前报道的更有希望。《小儿外科杂志》36:1792 - 1795。

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