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T细胞去除的骨髓移植后植入前的巨细胞病毒肺炎。

Cytomegalovirus pneumonia prior to engraftment following T-cell depleted bone marrow transplantation.

作者信息

Nagler A, Elishoov H, Kapelushnik Y, Breuer R, Or R, Engelhard D

机构信息

Department of Bone Marrow Transplantation, Hadassah University Hospital, Jerusalem, Israel.

出版信息

Med Oncol. 1994;11(3-4):127-32. doi: 10.1007/BF02999860.

Abstract

CMV pneumonia is a frequent complication of allogeneic bone marrow transplantation (BMT). It usually appears 23 months following transplantation and is associated with a high mortality rate. The incidence of CMV pneumonia in our T-lymphocyte depleted allogeneic BMT recipients, transplanted between 1987-1991, was 18 out of 197 (9.2%) patients. In 3 patients (1.5% of allogenic BMT recipients), pneumonia occurred prior to marrow engraftment, on days 12-16 post BMT. These patients did not develop acute GVHD in contrast to 9/11 patients who had acute GVHD in addition to developing CMV pneumonia between engraftment and day +100 (p < 0.03). Furthermore, these three patients did not receive steroid therapy as opposed to 14/15 patients who were treated with steroids and eventually contracted CMV pneumonia post-engraftment (p < 0.01). The three patients did not have two additional risk factors known for the development of CMV pneumonia: increasing age and a diagnosis of acute myeloblastic leukemia (AML) as the primary disease. Despite prompt diagnosis and therapy with ganciclovir and high doses of intravenous immunoglobulin (IVIG), two of the patients died. Tcell depleted BMT may be a risk factor for development of CMV pneumonia occurring prior to engraftment. In the era of post-BMT anti CMV prophylaxis, one should be aware that life-threatening CMV pneumonia may appear prior to engraftment and consider aggressive CMV prophylaxis.

摘要

巨细胞病毒肺炎是异基因骨髓移植(BMT)常见的并发症。它通常在移植后2 - 3个月出现,且死亡率很高。在1987年至1991年间接受移植的T淋巴细胞去除的异基因BMT受者中,巨细胞病毒肺炎的发生率为197例患者中的18例(9.2%)。在3例患者(占异基因BMT受者的1.5%)中,肺炎在骨髓植入前即BMT后第12 - 16天发生。与11例在植入后至+100天期间除发生巨细胞病毒肺炎外还发生急性移植物抗宿主病(GVHD)的患者中的9例相比,这些患者未发生急性GVHD(p < 0.03)。此外,这3例患者未接受类固醇治疗,而15例接受类固醇治疗并最终在植入后感染巨细胞病毒肺炎的患者中有14例接受了类固醇治疗(p < 0.01)。这3例患者没有已知的另外两个巨细胞病毒肺炎发生的危险因素:年龄增长和以急性髓细胞白血病(AML)作为原发性疾病的诊断。尽管及时诊断并使用更昔洛韦和高剂量静脉注射免疫球蛋白(IVIG)进行治疗,但仍有2例患者死亡。T细胞去除的BMT可能是植入前发生巨细胞病毒肺炎的一个危险因素。在BMT后抗巨细胞病毒预防的时代,应意识到在植入前可能出现危及生命的巨细胞病毒肺炎,并考虑积极的巨细胞病毒预防措施。

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