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Published on: September 19, 2025
Neonatal colonic mucormycosis--a tropical perspective
Priya Alexander1, Anand Alladi, Marjorie Correa
1Department of Pathology, St. John's Medical College and Hospital, Bangalore, India. priyaalexander@yahoo.com
Abstract:
Neonatal gastrointestinal (GI) mucormycosis is a rare, usually fatal, opportunistic fungal infection, which is difficult to diagnose early or preoperatively. We report three babies, only one of whom survived, with a review of the literature. All three had similar findings of necrosis of colon with multiple perforations. While the first baby was diagnosed as long segment Hirschsprung's, the second was treated as small left colon but went on to show signs of peritonitis. The third presented with pneumonia, which progressed to sepsis and peritonitis. All three were diagnosed by histology postoperatively and two of them succumbed, one in spite of amphotericin and the other as he was too sick to start antifungals and had a rapid downhill course. The one who survived did so even though she did not receive amphotericin, but had clear margins of resection. The only chance of survival in this fatal disease is early diagnosis and rapid institution of aggressive therapy inclusive of adequate surgical debridement and appropriate antifungal medications.
Insights
Neonatal gastrointestinal mucormycosis is a rare and often fatal fungal infection. Early diagnosis and aggressive treatment, including surgery and antifungals, are crucial for survival in infants.
Area of Science:
- Medical Mycology
- Neonatal Surgery
- Pediatric Infectious Diseases
Background:
- Neonatal gastrointestinal mucormycosis is a rare, opportunistic fungal infection.
- It is often fatal and challenging to diagnose preoperatively.
- This condition can present with severe gastrointestinal complications.
Purpose of the Study:
- To report three cases of neonatal gastrointestinal mucormycosis.
- To review the literature on this rare condition.
- To identify factors influencing survival.
Main Methods:
- Case series of three neonates with gastrointestinal mucormycosis.
- Histopathological diagnosis postoperatively.
- Literature review of similar cases.
Main Results:
- All three infants presented with colon necrosis and multiple perforations.
- Diagnoses included Hirschsprung's disease and small left colon syndrome initially.
- Two infants died despite or without antifungal treatment; one survived with clear surgical margins.
Conclusions:
- Early diagnosis and prompt, aggressive management are critical for survival.
- Surgical debridement and appropriate antifungal therapy are essential components of treatment.
- Successful outcomes depend on timely intervention and surgical resection.
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