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血液系统恶性肿瘤患者的毛霉菌病:一种新出现的真菌感染。

Mucormycoses in patients with hematologic malignancies: an emerging fungal infection.

作者信息

Bethge Wolfgang A, Schmalzing Marc, Stuhler Gernot, Schumacher Ulrike, Kröber Stefan-Martin, Horger Marius, Einsele Hermann, Kanz Lothar, Hebart Holger

机构信息

Medical Center University of Tübingen, Hematology/Oncology Otfried-Müller Str. 10 , 72076 Tübingen; Germany.

出版信息

Haematologica. 2005 Nov;90 Suppl:ECR22.

Abstract

BACKGROUND AND OBJECTIVES

Mucormycoses are seen with an increasing incidence in immunocompromised patients. Most common presentations are rhinocerebral and pulmonary. We here report the experience of a single center with mucormycoses in patients with hematologic malignancies.

RESULTS

Mucormycoses were diagnosed in six patients, (median age of 52 years; range, 26-74) treated between 2001-2004. Diagnoses included acute myeloid leukemia (AML) (n=3), acute lymphoblastic leukemia (n=1), chronic lymphocytic leukemia (n=1) and multiple myeloma (n=1). Mucormycosis was diagnosed in the neutropenic state following allogeneic hematopoietic cell transplantation (n=3) or intense chemotherapy (n=3). Sites of infections were rhinocerebral, facial and pulmonary involvement in one patient each and disseminated mucormycosis in three patients. The diagnosis was established by computed tomography followed by surgical interventions and histological diagnosis in 4 patients and post-mortem in two patients. Species identified were Rhizopus (n=3), Rhizomucor (n=2) and Absidia (n=1). Treatment responses were best if surgical resection was followed by aggressive antifungal chemotherapy. Five of six 6 patients died, all of complications of mucormycosis or their underlying disease. Only one patient with facial mucormycosis is still alive.

CONCLUSIONS

This experience demonstrates that patient with mucormycoses have a high mortality rate and early recognition followed by aggressive surgical debridement, high dose antifungal therapy and attempts to correct the underlying immunocompromised state are crucial in the treatment of this fatal infection.

摘要

背景与目的

毛霉病在免疫功能低下患者中的发病率呈上升趋势。最常见的表现为鼻脑型和肺型。我们在此报告一个单中心对血液系统恶性肿瘤患者毛霉病的治疗经验。

结果

2001年至2004年间,对6例患者(中位年龄52岁;范围26 - 74岁)进行了毛霉病诊断。诊断包括急性髓系白血病(AML)(n = 3)、急性淋巴细胞白血病(n = 1)、慢性淋巴细胞白血病(n = 1)和多发性骨髓瘤(n = 1)。毛霉病在异基因造血细胞移植(n = 3)或强化化疗(n = 3)后的中性粒细胞减少状态下被诊断。感染部位分别为1例鼻脑型、1例面部型和1例肺型,3例为播散性毛霉病。4例患者通过计算机断层扫描确诊,随后进行手术干预和组织学诊断,2例患者通过尸检确诊。鉴定出的菌种为根霉(n = 3)、根毛霉(n = 2)和犁头霉(n = 1)。如果手术切除后进行积极的抗真菌化疗,治疗反应最佳。6例患者中有5例死亡,均死于毛霉病并发症或其基础疾病。仅1例面部毛霉病患者存活。

结论

该经验表明,毛霉病患者死亡率高,早期识别并随后进行积极的手术清创、高剂量抗真菌治疗以及纠正潜在的免疫功能低下状态对于治疗这种致命感染至关重要。

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