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    µ¿ÀǾî=malignant schwannoma. ½´¹Ý ¼¼Æ÷¿¡¼­ ¹ßÇàÇÏ´Â ¾Ç¼º Á¾¾çÀ¸·Î¼­ óÀ½ºÎÅÍ ¾Ç¼ºÀ¸·Î ¹ß»ýÇÏ´Â °æ¿ìµµ ÀÖ°í ½´¹Ý ¼¼Æ÷ÀÇ ¾ç¼º Á¾¾ç¿¡¼­ ¾Ç¼ºÈ­¸¦ ÇÏ´Â °æ¿ìµµ ÀÖ´Ù. ºñ±³Àû µå¹® ÁúȯÀ̳ª ¾Ç¼ºµµ´Â ³ô°í À°¾ÈÀûÀ¸·Î ÇǸ·ÀÌ ¾øÀÌ Ä§½À¼º ¼ºÀåÀ» Çϸç Àý¸é¿¡¼­ ±«»ç¸¦ º¸ÀδÙ. Çö¹Ì°æÀûÀ¸·Î ¹æÃßÇü ¼¼Æ÷ÀÇ ³ó¿°µÈ ÇÙÀº ºÒ±ÔÄ¢ÇÏ°í ¸¹Àº À¯»çºÐ¿­ »óÀ» º¸ÀδÙ.
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neurofibrosarcoma A malignant tumour of neural sheath origin. Although superficially similar in appearance to fibrosarcoma, it is more aggressive and its cells are more variable in size and shape. The most common primary sites are the extremities, retroperitoneum, and trunk. It accounts for 5-10% of all non-rhabdomyosarcomatous soft tissue sarcomas in children. Neurofibrosarcoma often occurs in association with von recklinghausen's disease.
(12 Dec 1998)
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  • Neurofibrosarcoma - »õâ A malignant tumor that arises from small cutaneous nerves, is locally aggressive, and has a potential for metastasis. Characteristic histopathologic features include proliferating atypical spindle cells with slender wavy and pointed nuclei, hypocellular areas, and areas featuring organized whorls of fibroblastic proliferation. The most common primary sites are the extremities, retroperitoneum, and trunk. These tumors tend to present in childhood, often in association with NEUROFIBROMATOSIS 1. (From DeVita et al., Cancer: Principles & Practice of Oncology, 5th ed, p1662; Mayo Clin Proc 1990 Feb;65(2):164-72)
    Synonyms : Neurofibrosarcomas, Neurogenic Sarcoma, Neurogenic Sarcomas, Sarcomas, Neurogenic
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neurofibrosarcoma Malignant tumor of nerve sheath (also called malignant schwannoma).
Ãâó: www.understandingnf1.org/glossary/
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