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Macrophage Cholesterol Depletion and Its Effect on the Phagocytosis of Cryptococcus neoformans
Published on: December 19, 2014
Systemic cryptococcosis in an immune-competent child
Arushi G Saini1, Sooraj Patil1, Triptee Agrawal1
1Department of Pediatrics, Postgraduate Institute of Medical Education and Research, Chandigarh 160012, India.
Insights
This case report details disseminated cryptococcosis in an immunocompetent child. Early diagnosis and treatment of this rare fungal infection are crucial for patient survival.
Area of Science:
- Mycology
- Infectious Diseases
- Pediatrics
Background:
- Cryptococcus neoformans is an encapsulated yeast
- It commonly affects immunocompromised individuals
- Increasingly identified in immunocompetent hosts
Purpose of the Study:
- To report a rare case of disseminated cryptococcosis
- To highlight the presentation in a young, immunocompetent child
- To emphasize the importance of early diagnosis and management
Main Methods:
- Clinical presentation of a 4-year-old child with fever, abdominal pain, and skin lesions
- Diagnostic workup including imaging, bone-marrow aspiration, and fine-needle-aspiration-cytology
- Treatment with liposomal amphotericin-B, flucytosine, and fluconazole
Main Results:
- Fine-needle-aspiration-cytology confirmed Cryptococcus in cervical lymph nodes
- Serum latex-agglutination test showed a positive titer (1:256)
- Disseminated infection involved reticuloendothelial and dermatological systems
Conclusions:
- Disseminated cryptococcosis is rare in immunocompetent children
- Timely diagnosis and management are critical for favorable outcomes
- Infection requires prompt antifungal therapy to prevent severe complications
Abstract:
Crytococcus neoformans is an encapsulated yeast that frequently affects immune-compromised patients, although increasingly being detected in the immune-competent host as well. We report a case of disseminated cryptococcosis in a young child in whom no immune deficiency was yet identified. A 4-year-old child presented with high-grade fever, intermittent abdominal pain and generalized skin eruptions for the past two months. He had pallor, firm lymphadenopathy, skin lesions with scarring and firm hepatosplenomegaly. Magnetic resonance imaging of brain and bone-marrow aspiration were normal. Fine-needle-aspiration-cytology of cervical lymph nodes demonstrated Cryptococcus. Serum latex-agglutination test showed a positive titer (1:256). Cryptococcus culture was sterile. The patient received intravenous liposomal amphotericin-B and oral flucytosine for 8 weeks followed by oral fluconazole. Disseminated cryptococcosis with involvement of reticuloendothelial and dermatological systems is rare. Early diagnosis and timely management of associated complications would be life saving.
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