异基因造血干细胞移植后的胃肠道并发症:早期内镜评估的多学科方法。

Clinical Hematology International Pub Date : 2021-09-23 eCollection Date: 2021-12-01 DOI:10.2991/chi.k.210826.001
Giuseppe Tarantino, Francesco Saraceni, Giorgia Mancini, Monica Poiani, Luca Maroni, Gaia Goteri, Ilaria Scortechini, Alessandro Fiorentini, Maria Vittoria Dubbini, Francesco Marini, Luigi Daretti, Marco Marzioni, Emanuele Bendia, Antonio Benedetti, Attilio Olivieri
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引用次数: 8

摘要

胃肠道并发症(gic)是异体造血干细胞移植(allogenic hematopoietic stem cell transplantation, alloo - hsct)术后发病和死亡的主要原因。GICs的鉴别诊断至关重要,因为早期可靠地识别移植物抗宿主病(GVHD)对于正确治疗患者至关重要。本回顾性研究的目的是评估同种异体造血干细胞移植后GVHD的发生,并评估快速内镜和组织学评估在GVHD和其他胃肠道疾病鉴别诊断中的诊断作用。在2015年1月至2019年8月期间,122名连续接受同种异体造血干细胞移植的患者由一个跨学科团队管理,并由专门的内窥镜服务提供支持。对每位患者的临床、治疗、内镜和组织学资料进行分析。总的来说,94名患者发生了GICs(77%)。中重度粘膜炎是最常见的并发症,发生在79例患者中(84%)。35名患者被诊断为急性GI-GVHD(其中37%为gi患者),其中19名为中重度。8例患者发生感染性急性结肠炎,主要是由于艰难梭菌(CD)和巨细胞病毒感染(8.5%)。直肠活检显示最高的敏感性和特异性(分别为80%和100%)。然而,当活检过程以症状为指导并在表面完整的粘膜上进行时,上部组织学也提供了很高的阴性预测值(80%)。我们采用多学科方法,对接受同种异体造血干细胞移植并患有GICs的患者进行快速内窥镜/组织学检查,可以改善这种具有挑战性的环境下的诊断和治疗管理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Gastrointestinal Complications after Allogeneic Hematopoietic Stem Cell Transplant: A Multidisciplinary Approach with Early Endoscopic Evaluation.

Gastrointestinal complications (GICs) represent the major cause of morbidity and mortality after allogeneic hematopoietic stem cell transplantation (allo-HSCT). Differential diagnosis of GICs is of paramount importance since early and reliable identification of graft-versus-host disease (GVHD) is essential for a correct management of the patients. The aim of the present retrospective study was to evaluate the occurrence of GICs after allo-HSCT and to assess the diagnostic performance of a quick endoscopic and histological assessment in the differential diagnosis between GVHD and other GI conditions. Between January 2015 and August 2019, 122 consecutive patients receiving an allo-HSCT were managed by an interdisciplinary team, supported by a dedicated endoscopic service. Clinical, therapeutic, endoscopic and histological data were analyzed for each patient. Collectively, 94 of the patients developed GICs (77%). A moderate-severe mucositis was the most frequent complication, occurring in 79 patients (84%). Acute GI-GVHD was diagnosed in 35 patients (37% of whom with GICs) and 19 of them with a moderate-severe grade. Infective acute colitis developed in eight patients, mainly due to Clostridium difficile (CD) and Cytomegalovirus infections (8.5%). Rectal biopsy showed the highest sensitivity and specificity (80% and 100%, respectively). However, when biopsy procedures were guided by symptoms and performed on apparently intact mucosa, upper histology also provided a high negative predictive value (80%). Our multidisciplinary approach with a quick endoscopic/histologic investigation in the patients receiving an allo-HSCT and who suffered GICs could improve diagnostic and therapeutic management in this challenging setting.

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