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A CASE REPORT OF NEUROFIBROMA

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Ë©éÎÍÞ/Kang, Wou Ghon ì°ßÔÕÎ/ÚÓ÷ºê¹/Lee, Sang Rae/Park, Tae Won

Abstract


The authors have observed a rare case of neurofibroma in 13 years old male who came to the Infirmary of Dental college of Seoul National University becauseof painless severe swelling of approximately 11 years¢¥ duration in the left maxillofacial regin and blindeness of the left eye about 3 years¢¥ duration.
As a result of interpretating the serial roentgenograms including tomogrms and microscopic findings, we have botained the following conclusions;
1. Neurofibroma of the patient occurred inabout 2 years of age.
2. The familial tendency of the disease has been noted.
3. The growth pattern of the disease was slow, and roentgenographic images revealed severe destruction of bone with irregular borders.
4. The neurofibroma was encapsulated but Verocay body and palisading effect of cells were not seen in the microscopic picture.

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