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Pediatric fibroma in maxillary sinus following nasal trauma: A case report
1Dicle University Medical School, Department of Otolaryngology, Diyarbakir, Turkey.
Insights
Pediatric nasal fibroma, a rare benign tumor, can cause significant swelling and obstruction. Early diagnosis requires considering trauma history and combining clinical, radiological, and pathological findings.
Area of Science:
- Pediatric Oncology
- Otolaryngology
- Pathology
Background:
- Fibroma, a benign connective tissue tumor, presents diagnostic challenges in pediatric maxillary swellings.
- Maxillary swellings in children require careful differential diagnosis and surgical consideration.
Purpose of the Study:
- To report a case of nasal fibroma in a pediatric patient.
- To highlight diagnostic challenges and management strategies for pediatric nasal fibroma.
Main Methods:
- A 26-month-old girl presented with nasal swelling, obstruction, and dyspnea following head trauma.
- Endoscopic examination revealed nasal passage obstruction and lateral wall expansion.
- Surgical intervention involved Caldwell-Luc and transnasal endoscopic approaches.
- Pathological examination showed dense collagen fibers and fusiform fibroblasts.
Main Results:
- The case involved a rare pediatric nasal fibroma.
- Surgical intervention and pathological analysis confirmed the diagnosis.
- Clinicopathological correlation and imaging are crucial for diagnosis.
Conclusions:
- Fibroma and similar lesions are rare and diagnostically complex.
- Trauma history is critical in pediatric maxillofacial swelling cases.
- Integrated diagnostic approaches including imaging and pathology are essential.
Introduction:
Fibroma is a benign tumor of the connective tissue and is classified among the fibrous and fibrous histiocytic lesions. In the pediatric age group, both the differential diagnosis and surgery of maxillary swellings are difficult.
Case Reports:
A 26-month old girl applied with swelling and malformation in the nose. She complained of swelling in the right cheek, nasal obstruction and dyspnea during the night time. Her family stated that she had a head trauma 45 days before the application. We observed a rigid mass in the lateral side of the right nasal region consistent with severe edema. The pediatric endoscopic examination displayed a passage obstruction and an expansion of the lateral wall towards the septum. We performed right Caldwell-Luc approach with the endoscopic transnasal approach. The pathological examination with the light microscope displayed dense and thick collagen fibers and fusiform fibroblasts mixed up with these collagen fibers.
Discussion:
Fibroma and fibroma like lesions are rare and difficult to diagnose. In the Pubmed database, we did not encounter any large-scale study focused on this type of tumors except for some case reports of fibromyxoma. In respect of the findings in the literature, along with the pathological criteria, the clinicopathological correlation and radiological imaging may facilitate the diagnosis. Furthermore, a good cooperation with the patient and his/her family and a reliable history like trauma are also critical.
Conclusion:
The possibility of trauma should be definitively questioned during the history of pediatric patients, who applied with a maxillofacial swelling with the presence of persistent edema and differential diagnosis for the soft tissue tumors like fibroma should be considered.
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