Orbital infection due to Saksenaea loutrophoriformis in an immunocompetent adolescent: A case report
5 affiliations
- 1Department of Biology, Hakim Sabzevari University, Sabzevar, Iran
- 2Department of Pediatrics, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran
- 3Department of Parasitology and Mycology, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran
- 4Ophthalmology, Eye Research Center, Mashhad University of Medical Sciences, Mashhad, Iran
- 5Westerdijk Fungal Biodiversity Institute, Utrecht, The Netherlands
Abstract
Background and Purpose:: Mucormycosis is a rare fungal infection which can cause acute, disfiguring, and angioinvasive infections in immunocompromised patients with high mortality and morbidity rates. However, this study aimed to present the case of a healthy 7-year-old female.
Case presentation:: An immunocompetent female with orbital mucormycosis caused by Saksenaea loutrophoriformis from Mashhad, Iran was admitted to the hospital. This rare infection was the consequence of an injury due to a tree branch. The causative agent was identified by histopathology, routine mycological methods, and DNA sequencing of the Internal Transcribed Spacer 1 and 2 regions, including the intervening 5.8S gene and the partial large subunit region D1 and D2.
Results:: The patient was successfully treated with surgical debridement and antifungal treatment of amphotericin B and oral posaconazole.
Conclusion:: Molecular diagnosis is crucial in the absence of sporulation to avoid misidentification and late diagnosis. This report of a rare infection in an immunocompetent host is valuable for awareness of clinicians.
Related
- Prolonged Primary Cytomegalovirus Infection in an Immunocompetent Adult Successfully Treated With Valganciclovir
- Pulmonary infection caused by Nocardia cyriacigeorgica and influenza A virus coinfection in an immunocompetent patient : A case report
- Simultaneous Diffuse Alveolar Hemorrhage and Acute Myocarditis in an Immunocompetent Adult with a Human Metapneumovirus Infection
- Disseminated Klebsiella pneumoniae Infection Causing Multisystem Abscesses and Necrotising Fasciitis in an Immunocompetent Patient: A Case Report.
- Life-threatening diffuse alveolar hemorrhage associated with Rhinovirus infection and the potential role of corticosteroids in immunocompetent patients: Case reports.
BibTeX
@article{dolatabadi2026orbital,
title = {{Orbital infection due to Saksenaea loutrophoriformis in an immunocompetent adolescent: A case report}},
author = {Somayeh Dolatabadi and Mohammad Hasan Aelami and Mohammad Javad Najafzadeh and Mohammad Etezad Razavi and Mohammad Saeid Sasan and Jos Houbraken},
journal = {Current Medical Mycology},
year = {2026},
month = jun,
doi = {10.22034/cmm.2026.345464.1697},
url = {https://doi.org/10.22034/cmm.2026.345464.1697},
note = {CC BY 4.0},
}
RIS
TY - JOUR
TI - Orbital infection due to Saksenaea loutrophoriformis in an immunocompetent adolescent: A case report
AU - Somayeh Dolatabadi
AU - Mohammad Hasan Aelami
AU - Mohammad Javad Najafzadeh
AU - Mohammad Etezad Razavi
AU - Mohammad Saeid Sasan
AU - Jos Houbraken
PY - 2026
DA - 2026/06/26
JO - Current Medical Mycology
DO - 10.22034/cmm.2026.345464.1697
UR - https://doi.org/10.22034/cmm.2026.345464.1697
AB - Background and Purpose:: Mucormycosis is a rare fungal infection which can cause acute, disfiguring, and angioinvasive infections in immunocompromised patients with high mortality and morbidity rates. However, this study aimed to present the case of a healthy 7-year-old female. Case presentation:: An immunocompetent female with orbital mucormycosis caused by Saksenaea loutrophoriformis from Mashhad, Iran was admitted to the hospital. This rare infection was the consequence of an injury due to a tree branch. The causative agent was identified by histopathology, routine mycological methods, and DNA sequencing of the Internal Transcribed Spacer 1 and 2 regions, including the intervening 5.8S gene and the partial large subunit region D1 and D2. Results:: The patient was successfully treated with surgical debridement and antifungal treatment of amphotericin B and oral posaconazole. Conclusion:: Molecular diagnosis is crucial in the absence of sporulation to avoid misidentification and late diagnosis. This report of a rare infection in an immunocompetent host is valuable for awareness of clinicians.
SN - 2423-3439
SN - 2423-3420
ER -