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Mucormycosis in a case of multisystem inflammatory syndrome in children: "double trouble" (case report)
Keta Vagha1, Revat Meshram1, Sham Lohiya1
1Department of Pediatrics, Jawaharlal Nehru Medical College, Sawangi (Meghe), Wardha, Maharashtra, India.
Abstract:
Multisystem inflammatory syndrome (MIS-C) in the pediatric age group is a clinical syndrome in children and adolescents which is recognized in association with a high local prevalence of Corona Virus Disease-2019 (COVID-19). Mucormycosis is a severe form of fungal infection and often affects immunocompromised patients. It is associated with high morbidity and mortality and is characterized by extensive angioinvasion and necrosis of the affected tissue. Currently, this dreaded mucormycosis is rising among COVID-19 pediatric patients during their treatment period or after their discharge from the hospital. It is also called COVID-19- associated mucormycosis (CAM) or black fungus. In the head and neck area, rhino-orbital-cerebral mucormycosis is the most common presentation and a fatal clinical entity associated with COVID-19 infections. There are several cases of mucormycosis reported in cases with COVID-19 infection, but there is limited data available for the development of mucormycosis in MIS-C. Here, we report a case of a nine years old girl who developed mucormycosis while suffering from MIS-C. The patient was brought to our institute with complaints of fever for 3 days associated with redness of the eyes and swelling behind both ears and bilateral conjunctival congestion. Subsequently, she started showing signs of end organ damage in form oliguria and deranged liver function. Her COVID-19 antibody titer was positive and hence was diagnosed as MIS-C. She had prolonged hospitalization during which she started developing black discoloration over the nose. The histopathology report of the lesion was suggestive of mucormycosis. Eventually, the patient died due to multiple organ dysfunction. There is not only an association of mucormycosis in COVID-19- positive patients, but it shows some association with its complications like MIS-C. There is very limited data available for the association of mucormycosis and MIS-C but early diagnosis and intervention play a vital role in the outcome of the patient.
Insights
Multisystem inflammatory syndrome in children (MIS-C) is linked to mucormycosis, a severe fungal infection. This case highlights the risk of mucormycosis in pediatric MIS-C patients, emphasizing the need for early diagnosis and intervention.
Area of Science:
- Pediatric Infectious Diseases
- Mycology
- Critical Care Medicine
Background:
- Multisystem inflammatory syndrome in children (MIS-C) is a serious condition associated with COVID-19.
- Mucormycosis, a fungal infection, poses a high mortality risk, particularly in immunocompromised individuals.
- While mucormycosis is documented in COVID-19 patients, its occurrence in MIS-C is less understood.
Observation:
- A nine-year-old girl diagnosed with MIS-C presented with fever, eye redness, and swelling.
- She developed end-organ damage, including oliguria and liver dysfunction, during prolonged hospitalization.
- The patient subsequently developed a nasal lesion, confirmed as mucormycosis via histopathology.
Findings:
- The case demonstrates a fatal instance of mucormycosis in a pediatric patient with MIS-C.
- Histopathology confirmed mucormycosis, a severe fungal infection, in the nasal lesion.
- Despite medical intervention, the patient succumbed to multiple organ dysfunction.
Implications:
- This case suggests a potential association between MIS-C and the development of mucormycosis.
- Limited data exists on mucormycosis in MIS-C, underscoring the need for further research.
- Early recognition and prompt treatment of mucormycosis in MIS-C patients are crucial for improving outcomes.
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