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Published on: March 22, 2012
Neonatal Cutaneous Invasive Aspergillosis Accompanied by Hemophagocytic Lymphohistocytosis
Zhuanggui Chen1, Lifen Yang, Yating Li
1From the *Department of Pediatrics and †Department of Dermatology, Third Affiliated Hospital, Sun Yat-sen University, Guangzhou, China; ‡Institute of Biodiversity and Ecosystem Dynamics, University of Amsterdam, Amsterdam, the Netherlands; CBS-KNAW Fungal Biodiversity Centre, Utrecht, The Netherlands; Directorate General of Health Services, Ibri Hospital, Ministry of Health, Oman; and §Department of Medical Microbiology, Radboud University Nijmegen Medical Center, Nijmegen, The Netherlands; Department of Medical Microbiology and Infectious Diseases, Canisius Wilhelmina Hospital, Nijmegen, The Netherlands.
Abstract:
We describe a 6-week-old female infant with cutaneous invasive aspergillosis accompanied with hemophagocytic lymphohistocytosis. Aspergillus flavus was isolated from biopsies of necrotic skin lesions on the forehead and scalp; morphologic identification was confirmed by molecular analysis. In vitro antifungal susceptibility testing showed that amphotericin B and triazoles had potent activity. The patient responded well to treatment with intravenous amphotericin B combined with oral posaconazole and local wound care. The hemophagocytic lymphohistocytosis abated after treatment of cutaneous aspergillosis. Both cutaneous invasive aspergillosis and hemophagocytic lymphohistocytosis are severe disorders with high morbidity and mortality requiring prompt diagnosis and treatment.
Insights
A rare infant fungal infection, cutaneous invasive aspergillosis, was successfully treated with amphotericin B and posaconazole. This treatment also resolved associated hemophagocytic lymphohistiocytosis, highlighting the importance of prompt diagnosis and management.
Area of Science:
- Medical Mycology
- Pediatric Infectious Diseases
- Hematology
Background:
- Cutaneous invasive aspergillosis is a rare but severe fungal infection, particularly in infants.
- Hemophagocytic lymphohistiocytosis (HLH) is a life-threatening hyperinflammatory syndrome.
- Co-occurrence of these conditions presents significant diagnostic and therapeutic challenges.
Observation:
- A 6-week-old female infant presented with invasive aspergillosis of the skin.
- Aspergillus flavus was identified from skin lesion biopsies and confirmed molecularly.
- The infant also exhibited signs of hemophagocytic lymphohistiocytosis.
Findings:
- Antifungal susceptibility testing revealed potent activity of amphotericin B and triazoles against Aspergillus flavus.
- The infant showed a positive clinical response to intravenous amphotericin B, oral posaconazole, and wound care.
- Resolution of hemophagocytic lymphohistiocytosis was observed following successful treatment of the fungal infection.
Implications:
- Prompt diagnosis and treatment of cutaneous invasive aspergillosis are crucial for patient survival.
- Effective antifungal therapy can lead to the resolution of associated severe conditions like HLH.
- This case underscores the need for vigilance in diagnosing and managing invasive fungal infections in vulnerable pediatric populations.
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