Çмú´ëȸ ¹ßÇ¥ ¿¬Á¦ ÃÊ·Ï

¹ßÇ¥Çü½Ä : Å»¶ô Á¢¼ö¹øÈ£ - 980146    RHPX-14 
ALK-negative Inflammatory Myofibroblastic Neoplasm presenting as Maxillary Sinonasal Tumor in a 37 year old patient: A Case Report
1) DEP. OF OTORHINOLARYNGOLOGY-HEAD AND NECK SURGERY, ST. LUKES MEDICAL CENTER QUEZON CITY, 2) DEP. OF OTORHINOLARYNGOLOGY-HEAD AND NECK SURGERY, ST. LUKES MEDICAL CENTER QUEZON CITY 3) DEP. OF OTORHINOLARYNGOLOGY-HEAD AND NECK SURGERY, ST. LUKES MEDICAL CENTER QUEZON CITY
MARTIN CENON MAGADIA, MARTIN C. MAGADIA, DIANA R. FERNANDEZ, RONALDO G. SORIANO.
Objectives: To present a case of a inflammatory myofibroblastic neoplasm, sinonasal in origin, discuss its clinical features, and discuss diagnostic challenges encountered and management modalities done for the patient¡¯s case; review the current literature in diagnosis and treatment for inflammatory myofibroblastic neoplasm Case Report: A 37 year old male consulted for left facial swelling with a background of 3 month history of recurrent epistaxis. Office-based endoscopy and biopsy showed a fleshy mass that was friable and had brisk bleeding upon biopsy. Office-based biopsy showed chronic rhinosinusitis only. CT and MR imaging done had differential diagnoses including inverting papilloma, nasal angiofibroma, and inflammatory pseudotumor. A second endoscopic-guided biopsy under general anesthesia was done, with an initial diagnosis of spindle cell lesion. Open and endoscopic antero-medial maxillectomy was done and final histopathology showed inflammatory myofibroblastic neoplasm, ALK-negative. Conclusion: Inflammatory myofibroblastic neoplasm of the sinonasal region is a rare soft tissue tumor that remains to be studied in its behavior, diagnosis, and prognosis.


[´Ý±â]