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Beyond the Usual Suspects: Primary Premaxilla Sarcoidosis
Pankhuri Mittal1, Brijnandan Gupta2, Subodh Kumar3
1Department of ENT, All India Institute of Medical Sciences (AIIMS) Gorakhpur, India.
This case report details a rare instance of premaxillary sarcoidosis, a type of extrapulmonary sarcoidosis. Early diagnosis and complete surgical removal led to a successful outcome for the patient.
Area of Science:
- Maxillofacial Surgery
- Pathology
- Radiology
Background:
- Sarcoidosis is a systemic granulomatous disease with variable organ involvement.
- Extrapulmonary sarcoidosis, particularly in the premaxilla, is exceptionally rare.
- Diagnosis can be challenging due to non-specific symptoms and rarity.
Observation:
- A 62-year-old male presented with a three-year history of painless cheek swelling.
- Fine Needle Aspiration Cytology (FNAC) provided no definitive diagnosis.
- Contrast-enhanced CT scan identified a premaxillary soft tissue lesion.
Findings:
- Histopathological analysis of the excised lesion revealed non-caseating granulomas with asteroid bodies, confirming sarcoidosis.
- The patient had no evidence of systemic sarcoidosis.
- Complete surgical excision of the premaxillary lesion was achieved.
Implications:
- This case underscores the importance of considering rare diagnoses like premaxillary sarcoidosis in maxillofacial swelling.
- A multidisciplinary approach combining clinical, imaging, and histopathological evaluation is crucial for accurate diagnosis.
- Increased awareness of such presentations can improve diagnostic accuracy and patient management for extrapulmonary sarcoidosis.
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