急性淋巴细胞白血病治疗中侵袭性真菌病的治疗。

IF 0.9
Journal of medical cases Pub Date : 2025-05-01 Epub Date: 2025-05-28 DOI:10.14740/jmc5066
Ibrahim Alharbi, Amro Nassif, Yasser B Hennawi
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引用次数: 0

摘要

侵袭性真菌病(IFDs)是急性白血病(AL)患者死亡的主要原因之一。由于真菌复发的可能性,存活的ifd患者可能难以完成整个化疗计划。我们的病例报告提出了两例儿童前体b细胞急性淋巴细胞白血病(前b - all)的IFD合并曲霉病。2例9岁女性患者被诊断为b - all前期,采用b - all前期方案:CALL08, c组(高危组)和支持治疗。他们都在CALL08协议的Arm-C上(基于COG232的高风险)。然后,患者出现严重的发热性中性粒细胞减少症。患者1处于巩固期,患者2处于中期维持期。两例患者均出现了长期发热性中性粒细胞减少症。由于发热性中性粒细胞减少持续超过5天,进行了真菌检查,包括鼻窦、胸部和腹部的计算机断层扫描(CT),以及半乳甘露聚糖和(1→3)-β- d -葡聚糖(BDG)的血清检测。开始Caspofungin治疗。真菌检查结果显示1例患者肺和肝结节,另1例患者肺、肝和脾结节。尽管使用了广谱抗生素,但仍有大约4周的严重发烧和中性粒细胞减少。我们决定中断两名患者的化疗。在卡泊芬金中加入伏立康唑。活检证实诊断为严重真菌感染并侵袭性曲霉病。此后,高热和中性粒细胞减少症慢慢恢复,腹部反复CT扫描显示病变数量和大小均有良好改善。中断治疗6 - 8周后,继续化疗。我们观察到,在给予voriconazole和caspofungin联合抗真菌治疗6周后,再给予voriconazole口服单抗真菌治疗6周,两例患者均恢复正常,临床稳定且无发热。化疗暂时搁置,直到病情好转。总之,建议ALL患者进行一级和二级抗真菌预防。根据真菌感染的严重程度和疾病状况决定是否停止化疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Treatment of Invasive Fungal Disease During Therapy for Acute Lymphoblastic Leukemia.

Treatment of Invasive Fungal Disease During Therapy for Acute Lymphoblastic Leukemia.

Treatment of Invasive Fungal Disease During Therapy for Acute Lymphoblastic Leukemia.

Treatment of Invasive Fungal Disease During Therapy for Acute Lymphoblastic Leukemia.

Invasive fungal diseases (IFDs) are one of the leading causes of death in acute leukemia (AL) patients. Because of the possibility of fungal relapse, patients who survive IFDs may have difficulty in completing the whole chemotherapy plan. Our case report presents two cases of IFD with aspergillosis in children with precursor B-cell acute lymphoblastic leukemia (pre-B-ALL). Two 9-year-old female patients were diagnosed with pre-B-ALL that were on the pre-B-ALL protocol: CALL08, Arm-C (high-risk arm), and the supportive therapy. They were both on Arm-C of the CALL08 protocol (high risk based on COG232). Then, the patients experienced severe febrile neutropenia. Patient 1 was during consolidation, and patient 2 was during interim maintenance I. Both experienced prolonged febrile neutropenia. As febrile neutropenia continued for more than 5 days, a fungal workup was conducted, including computed tomography (CT) scans of the sinuses, chest, and abdomen, as well as serum tests for galactomannan and (1→3)-β-D-glucan (BDG). Caspofungin treatment was started. Fungal workup results showed lung and liver nodules in one patient and lungs, liver, and spleen in the other. There were about 4 weeks of severe fevers and neutropenia, despite the use of broad-spectrum antibiotics. A decision was taken to interrupt chemotherapy for both patients. Voriconazole was added to caspofungin. Biopsies confirmed the diagnosis to be severe fungal infection with invasive aspergillosis. After that, high fevers and neutropenia slowly recovered, and a repeated CT scan of abdomen showed good improvement in the lesion's number and size. After 6 - 8 weeks of interruption, chemotherapy was resumed. We observed that with the implementation of combination antifungal therapy with voriconazole and caspofungin for 6 weeks and then single antifungal therapy (voriconazole orally) for another 6 weeks, both patients recovered and became clinically stable and afebrile. Chemotherapy was on hold till they became better. In conclusion, primary and secondary antifungal prophylaxis are recommended for ALL patients. Chemotherapy discontinuation is decided on an individual basis according to the severity of the fungal infection and disease status.

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