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儿童移植后淋巴组织增生性疾病:与肝移植受者相比,造血细胞移植受者的表现。

Posttransplantation lymphoproliferative disorder in children: manifestations in hematopoietic cell recipients in comparison with liver recipients.

机构信息

Department of Radiology, Samsung Medical Center, Sungkyunkwan University School of Medicine, 50 Ilwon-dong, Gangnam-gu, Seoul 135-710, Korea.

出版信息

Radiology. 2010 Nov;257(2):490-7. doi: 10.1148/radiol.10092389. Epub 2010 Sep 9.

Abstract

PURPOSE

To compare the clinical and imaging features of posttransplantation lymphoproliferative disorder (PTLD) in pediatric patients who underwent hematopoietic cell transplantation with those in pediatric patients who underwent liver transplantation.

MATERIALS AND METHODS

This study was approved by the institutional review board, and the requirement to obtain informed consent was waived. The authors retrospectively reviewed the medical records and images of 552 hematopoietic cell transplant recipients and 195 liver transplant recipients. PTLD was histopathologically confirmed in 17 of the patients who underwent hematopoietic cell transplantation and 27 of the patients who underwent liver transplantation. The overall frequency, clinical course, histopathologic type, and imaging findings of PTLD were compared between the two patient groups by using the Fisher exact test.

RESULTS

The overall frequency of PTLD was 3% (17 of 552 patients) after hematopoietic cell transplantation (12% [nine of 75 patients] after umbilical cord blood transplantation) and 14% (27 of 194 patients) after liver transplantation. PTLD occurred within 6 months of transplantation in 14 of the 17 hematopoietic cell recipients (82%) and 11 of the 27 liver recipients (41%) (P = .012). Histopathologic examination revealed monomorphic disease in 11 of the 17 hematopoietic cell recipients (65%) and eight of the 27 liver recipients (30%) (P = .031). The abdomen was the most common site of involvement in both groups. Extraabdominal PTLD developed in 12 of the 17 hematopoietic cell recipients (71%) and five of the 27 liver recipients (19%) (P = .002). Although 15 of the 17 patients with hematopoietic cell transplantation-related PTLD (88%) exhibited responses after treatment, the overall mortality rate was 35% (six of 17 patients). All 27 patients with PTLD after liver transplantation improved after treatment and remain alive.

CONCLUSION

PTLD after umbilical cord blood transplantation occurred as frequently as liver transplantation-related PTLD. Compared with liver transplantation-related PTLD, PTLD after hematopoietic cell transplantation is characterized by an earlier onset, a higher proportion of malignant monomorphic disease, and a worse outcome.

摘要

目的

比较儿童造血细胞移植后与肝移植后发生的移植后淋巴组织增生性疾病(PTLD)的临床和影像学特征。

材料与方法

本研究经机构审查委员会批准,且豁免了获得知情同意的要求。作者回顾性分析了 552 例造血细胞移植受者和 195 例肝移植受者的病历和影像学资料。17 例造血细胞移植受者和 27 例肝移植受者经组织病理学证实为 PTLD。采用 Fisher 确切检验比较两组患者的 PTLD 总发生率、临床病程、组织病理学类型和影像学表现。

结果

造血细胞移植后 PTLD 的总发生率为 3%(552 例患者中有 17 例)[脐带血移植后为 12%(75 例患者中有 9 例)],肝移植后为 14%(194 例患者中有 27 例)。17 例造血细胞移植受者中有 14 例(82%)和 27 例肝移植受者中有 11 例(41%)在移植后 6 个月内发生 PTLD(P =.012)。17 例造血细胞移植受者中有 11 例(65%)和 27 例肝移植受者中有 8 例(30%)的组织病理学检查显示为单形性疾病(P =.031)。两组中腹部均为最常见的受累部位。17 例造血细胞移植相关 PTLD 中有 12 例(71%)和 27 例肝移植相关 PTLD 中有 5 例(19%)发生了腹外 PTLD(P =.002)。尽管 17 例造血细胞移植相关 PTLD 中有 15 例(88%)经治疗后有反应,但总体死亡率为 35%(17 例患者中有 6 例)。27 例肝移植后发生 PTLD 的患者经治疗后均有改善并存活。

结论

与肝移植相关的 PTLD 相比,脐带血移植后发生的 PTLD 更为常见。与肝移植相关的 PTLD 相比,造血细胞移植后发生的 PTLD 发病更早,恶性单形性疾病比例更高,预后更差。

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