Department of Pediatrics, Faculty of Medicine, Vajira Hospital, Navamindradhiraj University, Thailand.
*Corresponding Author : Thiraporn Kanjanaphan
Department of Pediatrics, Faculty of Medicine, Vajira Hospital, Navamindradhiraj university, Thailand.
Tel: +66955192942;
Email: [email protected]
Received : Dec 27, 2023
Accepted : Jan 16, 2024
Published : Jan 23, 2024
Archived : www.jcimcr.org
Copyright : © Kanjanaphan T (2024).
An 8-year-old Thai boy presented with a two-week history of anemia, abnormal purpura in both legs, and was diagnosed with B-cell acute lymphoblastic leukemia (B-cell ALL). Following Thai-POG guidelines, he underwent chemotherapy and received trimethoprim-sulfamethoxazole prophylaxis. However, he developed febrile neutropenia and, despite initial treatment with intravenous meropenem and amikacin, showed no improvement. After a week of febrile neutropenia, a chest CT scan revealed multiple lung nodules (Figure1a). Bronchoalveolar lavage confirmed a positive galactomannan level (1.12 ng/mL). The patient received voriconazole with therapeutic drug monitoring (level: 4.7 ug/mL). Despite this, he experienced progressive dyspnea and hypoxia, and a chest X-ray revealed bilateral ground glass appearance in the lower lungs (Figure 1b). Sputum analysis detected Pneumocystis Jirovecii Pneumonia (PJP) (Figure 1c). Treatment included trimethoprim-sulfonamides, prednisolone, and voriconazole. Within two days, the patient’s symptoms improved. Treatment duration for PJP was 21 days, followed by continued trimethoprim-sulfonamides prophylaxis. Voriconazole was maintained until resolution confirmed by imaging (approximately 6 months). The clinical manifestations of aspergillus infection vary, including ABPA, aspergilloma, chronic aspergillosis, and invasive aspergillosis [1]. Neutropenia duration correlates with the risk of invasive pulmonary aspergillosis [2]. Pneumocystis jirovecii is an opportunistic pathogen, affecting about 12% of children with acute lymphocytic leukemia [3]. A British study reported a 7% annual increase in PJP cases, deaths, and hospital admissions in England from 2000 to 2010 [4]. Both IPA and PJP pose significant threats to immunocompromised children. Although coinfection is rare, this case underscores the importance of a multidisciplinary approach, timely identification, and appropriate interventions for successful outcomes.
Declarations of competing interest: The authors have no competing interests to declare.
Funding statement: Not applicable.
Ethical approval and patient consent statement: Ethics approval and consent from Institutional Review Board Faculty of Medicine Vajira Hospital (COE:020/2023X).