Management of CMV Pneumonia, DAH, and BOS Following HSCT in a Child with β-Thalassemia: A Case Report

Li Li, Ting Chen, Yimei Feng, Peiyan Kong, Xi Zhang Medical Center of Hematology, The Second Affiliated Hospital of Army Medical University, Chongqing, 400037, People’s Republic of ChinaCorrespondence: Yimei Feng, Medical Center of Hematology, The Second Affiliated Hospital of Army Medical University, Chongqing, 400037, People’s Republic of China, Email [email protected] Correspondence: Peiyan Kong, Medical Center of Hematology, The Second Affiliated Hospital of Army Medical University, Chongqing, 400037, People’s Republic of China, Email [email protected]: Allogeneic hematopoietic stem cell transplantation (allo-HSCT) is a curative treatment for thalassemia major but carries a high risk of post-transplant complications. We report a pediatric case with β-thalassemia major who developed steroid-refractory grade III acute graft-versus-host disease (aGVHD) after HLA-9/10 mismatched unrelated donor allo-HSCT. This was followed by cytomegalovirus (CMV) reactivation that progressed to severe CMV pneumonia complicated by diffuse alveolar hemorrhage (DAH). Notably, after failure of first-line antiviral therapy, a combination of ganciclovir and letermovir was employed, resulting in complete virologic clearance and marked respiratory improvement. During follow-up, bronchiolitis obliterans syndrome (BOS) was diagnosed on day +154. The patient received repeated infusions of umbilical cord-derived mesenchymal stromal cells (UC-MSCs), initially for refractory intestinal aGVHD and later in conjunction with the FAM regimen (fluticasone, azithromycin, montelukast) for BOS, ultimately achieving full clinical recovery. This case highlights two key management insights: (1) the ganciclovir–letermovir combination can be effective in pediatric refractory CMV pneumonia, and (2) sequential UC-MSC administration may contribute to controlling both acute GVHD and late pulmonary complications. Finally, multidisciplinary collaboration and individualized strategies are essential in managing such complex post-transplant pulmonary syndromes in children.Keywords: pulmonary complications, HSCT, cytomegalovirus pneumonia, DAH, BOS

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Dove Medical Press (Taylor and Francis Group)
Published
2026-02-23
Primary Topic
Hematopoietic Stem Cell Transplantation
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article

Management of CMV Pneumonia, DAH, and BOS Following HSCT in a Child with β-Thalassemia: A Case Report

Peiyan Kong, Xi Zhang, Ting Chen, Li Li et al.
Dove Medical Press (Taylor and Francis Group)
Hematopoietic Stem Cell Transplantation
article

Management of CMV Pneumonia, DAH, and BOS Following HSCT in a Child with β-Thalassemia: A Case Report

Peiyan Kong, Xi Zhang, Ting Chen, Li Li, Yimei Feng
article en

Abstract

Li Li, Ting Chen, Yimei Feng, Peiyan Kong, Xi Zhang Medical Center of Hematology, The Second Affiliated Hospital of Army Medical University, Chongqing, 400037, People’s Republic of ChinaCorrespondence: Yimei Feng, Medical Center of Hematology, The Second Affiliated Hospital of Army Medical University, Chongqing, 400037, People’s Republic of China, Email [email protected] Correspondence: Peiyan Kong, Medical Center of Hematology, The Second Affiliated Hospital of Army Medical University, Chongqing, 400037, People’s Republic of China, Email [email protected]: Allogeneic hematopoietic stem cell transplantation (allo-HSCT) is a curative treatment for thalassemia major but carries a high risk of post-transplant complications. We report a pediatric case with β-thalassemia major who developed steroid-refractory grade III acute graft-versus-host disease (aGVHD) after HLA-9/10 mismatched unrelated donor allo-HSCT. This was followed by cytomegalovirus (CMV) reactivation that progressed to severe CMV pneumonia complicated by diffuse alveolar hemorrhage (DAH). Notably, after failure of first-line antiviral therapy, a combination of ganciclovir and letermovir was employed, resulting in complete virologic clearance and marked respiratory improvement. During follow-up, bronchiolitis obliterans syndrome (BOS) was diagnosed on day +154. The patient received repeated infusions of umbilical cord-derived mesenchymal stromal cells (UC-MSCs), initially for refractory intestinal aGVHD and later in conjunction with the FAM regimen (fluticasone, azithromycin, montelukast) for BOS, ultimately achieving full clinical recovery. This case highlights two key management insights: (1) the ganciclovir–letermovir combination can be effective in pediatric refractory CMV pneumonia, and (2) sequential UC-MSC administration may contribute to controlling both acute GVHD and late pulmonary complications. Finally, multidisciplinary collaboration and individualized strategies are essential in managing such complex post-transplant pulmonary syndromes in children.Keywords: pulmonary complications, HSCT, cytomegalovirus pneumonia, DAH, BOS

Dove Medical Press (Taylor and Francis Group)
Openalex Percentile: Top 45%
Hematopoietic Stem Cell Transplantation
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