Laryngeal squamous cell carcinoma in a 4-year-Old child: A rare case report
Mukhtar Baryare Matan1, Abdullahi Ahmed Tahlil2, Nafisa Ahmed Mohamed1
1Pediatric Intensive Care Unit, Department of Pediatrics, Benadir Maternity and Child Hospital, Mogadishu, Somalia.
Insights
This case report details a rare instance of laryngeal squamous cell carcinoma (LSCC) in a 4-year-old boy. Early detection and vigilance are crucial for treating this uncommon pediatric malignancy.
Area of Science:
- Pediatric Oncology
- Otolaryngology
- Cancer Research
Background:
- Laryngeal squamous cell carcinoma (LSCC) is exceptionally rare in children, representing less than 1% of pediatric head and neck cancers.
- This report focuses on a 4-year-old boy with a prolonged history of respiratory distress and stridor.
Observation:
- Initial assessment revealed a whitish lesion on the left vocal cord and posterior commissure via indirect laryngoscopy.
- The lesion was initially misdiagnosed as juvenile papillomatosis before surgical removal.
Findings:
- Histopathology confirmed superficially invasive squamous cell carcinoma of the larynx (LSCC).
- Microscopic examination showed acanthotic stratified squamous epithelium with significant pleomorphism and lamina propria invasion.
Implications:
- Highlights the critical need for early diagnosis and prompt treatment of pediatric laryngeal cancer.
- Underscores the importance of clinician awareness for respiratory symptoms in children, given the potential for rare malignancies.
- Contributes to the limited body of literature on LSCC in pediatric populations.
Abstract:
Laryngeal Squamous Cell Carcinoma (LSCC) is an extremely rare malignancy cancer in children, accounting for less than 1 % of head and neck cancers in those under 18. This case report discusses a 4-year-old boy with a three-year history of worsening respiratory distress and stridor, who was ultimately diagnosed with superficially invasive squamous cell carcinoma of the larynx. The child showed significant symptoms that led to further assessment. Indirect laryngoscopy revealed a whitish lesion on the left vocal cord and posterior commissure. Microlaryngoscopy under general anesthesia allowed complete removal of the lesion, initially thought to be juvenile papillomatosis. However, histopathology confirmed LSCC, showing acanthotic stratified squamous epithelium with marked pleomorphism and lamina propria invasion. This case emphasizes the importance of early detection and treatment of pediatric laryngeal cancer, despite its rarity and the risk of misdiagnosis. It adds to the limited literature on this condition and underscores the need for clinicians to remain vigilant when evaluating respiratory symptoms in children.
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