Alharbi Ibrahim, Nassif Amro, Hennawi Yasser B
Department of Pediatrics, Umm Al-Qura University, Makkah, Saudi Arabia.
Pediatric Division, Department of Pediatrics, King Fahad Armed Forces Hospital, Jeddah, Saudi Arabia.
J Med Cases. 2025 May;16(5):174-180. doi: 10.14740/jmc5066. Epub 2025 May 28.
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.
侵袭性真菌病(IFD)是急性白血病(AL)患者的主要死亡原因之一。由于存在真菌复发的可能性,IFD存活患者可能难以完成整个化疗计划。我们的病例报告介绍了两例前体B细胞急性淋巴细胞白血病(pre - B - ALL)儿童患IFD合并曲霉病的病例。两名9岁女性患者被诊断为pre - B - ALL,正在接受pre - B - ALL方案:CALL08,C组(高危组)及支持性治疗。她们均在CALL08方案的C组(基于COG232为高危组)。随后,两名患者均出现严重的发热性中性粒细胞减少。患者1处于巩固期,患者2处于中期维持治疗I期。两人均经历了长时间的发热性中性粒细胞减少。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。开始使用卡泊芬净治疗。真菌检查结果显示,一名患者肺部和肝脏有结节,另一名患者肺部、肝脏和脾脏有结节。尽管使用了广谱抗生素,仍有大约4周的严重发热和中性粒细胞减少。决定两名患者均中断化疗。在卡泊芬净基础上加用伏立康唑。活检确诊为严重真菌感染合并侵袭性曲霉病。此后,高热和中性粒细胞减少逐渐恢复,腹部CT复查显示病灶数量和大小有明显改善。中断6 - 8周后,恢复化疗。我们观察到,在实施伏立康唑和卡泊芬净联合抗真菌治疗6周,然后再单独使用抗真菌治疗(口服伏立康唑)6周后,两名患者均康复,临床症状稳定且无发热。化疗暂停直至患者病情好转。总之,建议对所有ALL患者进行一级和二级抗真菌预防。化疗的中断应根据真菌感染的严重程度和疾病状态个体化决定。