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수술 후 Horner 증후을 동반한 경부 자율신경초종 1예
조재구,송종석,우정수,이흥만 대한이비인후과학회 2004 대한이비인후과학회지 두경부외과학 Vol.47 No.3
slow-growing mass, and its malignant degeneration is rare. Recently, we experienced a case of schwannoma arising from cervical sympathetic chain. A 43-year-old woman presented a left neck mas that was found incidentally. Measuring approximately 3× 3 cm, the mas was located medial to the left sternocleidomastoid muscle at the level of the carotid bifurcation. Fine needle aspira-tion biopsy was performed, but no diagnostic information was given. A computed tomography (CT) scan showed a heterogenous, jugular vein laterally. Tumor was excised via transcervical approach. Postoperatively, the patient exhibited mild miosis with ptosis in the left eye. We report this case with a brief review of literature. (Korean J Otolaryngol 2004 ;47 :279-81)
조재구,최창재,정진호,우정수 대한이비인후과학회 2009 대한이비인후과학회지 두경부외과학 Vol.52 No.12
Inflammatory myofibroblastic tumor is an uncommon tumor composed of myofibroblasts and various types of inflammatory infiltrates that rarely undergoes malignant transformation. It commonly involves the lung, liver, mesentery but rarely affects the head and neck region. Although inflammatory myofibroblastic tumor is generally considered a benign reactive inflammatory process, it may present clinically and radiologically as an invasive mass destructing the surrounding structures. Therefore, it should be considered as one of several differential diagnoses from malignant tumors. We present a case of inflammatory myofibroblastic tumor involving the nasal cavity, maxillary, ethmoid, and sphenoid sinus with a fatal outcome.