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Updated: Jun 2, 2026

Derivation of Hematopoietic Stem Cells from Murine Embryonic Stem Cells
Published on: February 25, 2007
Rhizomucor and scedosporium infection post hematopoietic stem-cell transplant
Dânia Sofia Marques1, Carlos Pinho Vaz, Rosa Branca
1Bone Marrow Transplantation Service, Instituto Português de Oncologia Francisco Gentil, Rua Dr. António Bernardino de Almeida, 4200-072 Porto, Portugal.
Abstract:
Hematopoietic stem-cell transplant recipients are at increased risk of developing invasive fungal infections. This is a major cause of morbidity and mortality. We report a case of a 17-year-old male patient diagnosed with severe idiopathic acquired aplastic anemia who developed fungal pneumonitis due to Rhizomucor sp. and rhinoencephalitis due to Scedosporium apiospermum 6 and 8 months after undergoing allogeneic hematopoietic stem-cell transplant from an HLA-matched unrelated donor. Discussion highlights risk factors for invasive fungal infections (i.e., mucormycosis and scedosporiosis), its clinical features, and the factors that must be taken into account to successfully treat them (early diagnosis, correction of predisposing factors, aggressive surgical debridement, and antifungal and adjunctive therapies).
Insights
Hematopoietic stem-cell transplant recipients face high risks of invasive fungal infections. This case highlights rare Rhizomucor and Scedosporium infections post-transplant, emphasizing early diagnosis and treatment.
Area of Science:
- Medical Mycology
- Transplant Infectious Diseases
- Hematology
Background:
- Hematopoietic stem-cell transplantation (HSCT) recipients are immunocompromised, increasing susceptibility to opportunistic infections.
- Invasive fungal infections (IFIs) pose a significant threat, contributing to morbidity and mortality in this patient population.
- Aplastic anemia is a condition requiring intensive treatment, including HSCT, which further elevates infection risk.
Observation:
- A 17-year-old male with severe aplastic anemia developed invasive fungal infections 6 and 8 months post-allogeneic HSCT.
- The patient experienced fungal pneumonitis caused by Rhizomucor sp. and rhinoencephalitis caused by Scedosporium apiospermum.
- These infections occurred despite HSCT from an HLA-matched unrelated donor.
Findings:
- The case illustrates rare co-infections with distinct fungal pathogens, Rhizomucor (mucormycosis) and Scedosporium (scedosporiosis), in an HSCT recipient.
- Clinical presentation included pulmonary and central nervous system involvement, underscoring the diverse manifestations of IFIs.
- Risk factors for IFIs in HSCT recipients, such as prolonged neutropenia and graft-versus-host disease, are critical considerations.
Implications:
- Early and accurate diagnosis of IFIs, including identification of specific fungal agents, is crucial for effective management.
- Integrated treatment strategies involving antifungal therapy, surgical intervention, and addressing predisposing factors are essential for improving outcomes.
- This case emphasizes the need for heightened vigilance and tailored antifungal prophylaxis/treatment protocols for HSCT recipients at risk for mucormycosis and scedosporiosis.
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