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肺移植受者移植后淋巴细胞增生性疾病的胃肠道受累:一例报告

Gastrointestinal involvement of posttransplant lymphoproliferative disorder in lung transplant recipients: report of a case.

作者信息

Shitrit David, Shitrit Ariella Bar-Gil, Dickman Ram, Sahar Gidon, Saute Milton, Kramer Mordechai R

机构信息

Pulmonary Institute, Rabin Medical Center, Beilinson Campus, Petah Tiqwa, Israel.

出版信息

Dis Colon Rectum. 2005 Nov;48(11):2144-7. doi: 10.1007/s10350-005-0116-7.

Abstract

PURPOSE

Lymphoproliferative disorder is a well-recognized complication of lung transplantation. Risk factors include Epstein-Barr virus infection and immunosuppression. The gastrointestinal manifestations of post-transplant lymphoproliferative disorder in lung transplant recipients have not been fully characterized.

METHODS

Case presentation and 16 previously reported cases of post-transplant lymphoproliferative disorder with gastrointestinal involvement are reviewed.

RESULTS

Patient ages ranged from 25 to 65 (median, 52) years. Median time from lung transplantation to onset of posttransplant lymphoproliferative disorder was 36 (range, 1-109) months; 35 percent of cases (6/17) occurred within 18 months; Eighty-eight percent of patients (15/17) had positive Epstein-Barr virus serology before transplantation. In five patients (29 percent), the posttransplant lymphoproliferative disorder also involved sites other than the gastrointestinal tract. The most common gastrointestinal site of posttransplant lymphoproliferative disorder was the colon, followed by the small intestine and stomach. Clinical features included abdominal pain, nausea, and bloody diarrhea. Diagnosis was based on typical pathologic changes on gastrointestinal tract biopsy obtained mainly by colonoscopy. Treatment included a reduction in the immunosuppressive regimen in 15 of 17 cases (88 percent) and surgical resection in 10 (59 percent). One patient was untreated. Seven of 16 patients (44 percent) responded to treatment and 9 patients died. Median time from onset of posttransplant lymphoproliferative disorder to death was 70 (range, 10-85) days.

CONCLUSIONS

Posttransplant lymphoproliferative disorder with gastrointestinal involvement is a unique entity that should be considered in all Epstein-Barr-Virus-positive lung transplant recipients who present with abdominal symptoms. Although immunosuppressive modulation and resection can lead to remission, the risk of death is 50 percent.

摘要

目的

淋巴增生性疾病是肺移植公认的并发症。危险因素包括爱泼斯坦-巴尔病毒感染和免疫抑制。肺移植受者移植后淋巴增生性疾病的胃肠道表现尚未完全明确。

方法

回顾病例报告及16例先前报道的有胃肠道受累的移植后淋巴增生性疾病病例。

结果

患者年龄25至65岁(中位数52岁)。从肺移植到移植后淋巴增生性疾病发病的中位时间为36个月(范围1至109个月);35%的病例(6/17)在18个月内发病;88%的患者(15/17)移植前爱泼斯坦-巴尔病毒血清学呈阳性。5例患者(29%)的移植后淋巴增生性疾病还累及胃肠道以外的部位。移植后淋巴增生性疾病最常见的胃肠道部位是结肠,其次是小肠和胃。临床特征包括腹痛、恶心和血性腹泻。诊断主要基于通过结肠镜检查获取的胃肠道活检典型病理变化。治疗包括17例中的15例(88%)减少免疫抑制方案,10例(59%)进行手术切除。1例患者未接受治疗。16例患者中的7例(44%)对治疗有反应,9例患者死亡。从移植后淋巴增生性疾病发病到死亡的中位时间为70天(范围10至85天)。

结论

有胃肠道受累的移植后淋巴增生性疾病是一种独特的疾病实体,所有出现腹部症状的爱泼斯坦-巴尔病毒阳性肺移植受者均应考虑。尽管免疫抑制调整和切除可导致缓解,但死亡风险为50%。

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