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Severe Palatal Myiasis in a Young Patient With Neurological and Physical Disabilities: A Case Report
Marcelo Santos Bahia1, Yuri de Lima Medeiros2, Luan Viana Faria3
1Department of Oral and Maxillofacial Surgery and Periodontology, Ribeirão Preto School of Dentistry, University of São Paulo, Ribeirão Preto, São Paulo, Brazil.
Insights
This case study details severe palatal myiasis in a neurologically impaired pediatric patient. Prompt diagnosis and multidisciplinary care are crucial for managing this rare condition in vulnerable populations.
Area of Science:
- Medical Entomology
- Clinical Case Study
- Pediatric Neurology
Background:
- Myiasis poses significant challenges in pediatric patients with neurological impairments due to communication difficulties.
- Delayed diagnosis and treatment can exacerbate the debilitating effects of myiasis.
Observation:
- A 16-year-old female with neurological deficits presented with fever and an oral lesion.
- Diagnosis revealed bacterial pneumonia, palatal myiasis with larval migration, and dyspnea.
Findings:
- Larval myiasis was confirmed in the hard and soft palate.
- Treatment involved manual larva removal, antibiotics (ceftriaxone, clindamycin), ivermectin, and topical nitrofurazone.
- Surgical debridement addressed necrotic tissue, with no further larvae detected.
Implications:
- Severe palatal myiasis requires prompt diagnosis and a multidisciplinary approach.
- Management is complex in patients with physical/cognitive disabilities and challenging socioeconomic conditions.
Aims:
Myiasis can be particularly debilitating in pediatric patients with neurological impairments, as communication challenges in expressing symptoms may delay diagnosis and appropriate treatment. We report a case of palatal myiasis in a young Latin American patient with neurological deficits.
Methods And Results:
A 16-year-old female with a history of severe meningitis, which resulted in neurological sequelae including spastic paralysis and epilepsy, presented with an oral lesion in the buccal cavity and episodes of fever. Upon admission, she was diagnosed with bacterial pneumonia, multiple foci of myiasis in the hard and soft palate, and dyspnea caused by larval migration to the oropharyngeal region. Larvae were manually removed, and the patient was treated with intravenous ceftriaxone, clindamycin, and ivermectin. Nitrofurazone paste was also applied topically. Four days later, surgical debridement was performed to remove necrotic mucosa from the palate. No further larvae were detected, and the patient's condition stabilized. The patient has been under follow-up for 1 year.
Conclusion:
Severe palatal myiasis is a rare condition that demands prompt diagnosis and a multidisciplinary approach. This case highlights the complexity of managing myiasis in patients with physical and cognitive disabilities, especially in unfavorable socioeconomic conditions.
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