두개골 유아 근섬유증 - 증례보고 -

Infantile Myofibromatosis of the Skull - Case Report -

  • 박병준 (인제대학교 의과대학 서울백병원 신경외과학교실) ;
  • 고영초 (인제대학교 의과대학 서울백병원 신경외과학교실) ;
  • 유헌 (인제대학교 의과대학 서울백병원 신경외과학교실) ;
  • 이채혁 (인제대학교 의과대학 서울백병원 신경외과학교실) ;
  • 박효일 (인제대학교 의과대학 서울백병원 신경외과학교실)
  • Park, Byoung Jun (Department of Neurosurgery, Seoul Paik Hospital, College of Medicine, Inje University) ;
  • Koh, Young Cho (Department of Neurosurgery, Seoul Paik Hospital, College of Medicine, Inje University) ;
  • Yoo, Heon Yoo (Department of Neurosurgery, Seoul Paik Hospital, College of Medicine, Inje University) ;
  • Lee, Chea Heuck (Department of Neurosurgery, Seoul Paik Hospital, College of Medicine, Inje University) ;
  • Park, Hyo Il (Department of Neurosurgery, Seoul Paik Hospital, College of Medicine, Inje University)
  • 투고 : 1999.08.27
  • 심사 : 1999.12.02
  • 발행 : 2000.03.28

초록

Infantile myofibromatosis is a rare and benign myofibroblastic tumor that may occur in either solitary or multicentric form in the soft tissue of infants. A 13-month-old girl presented with a painless firm mass, measuring $2.5{\times}2.5cm$ in the right temporal area. Skull X-ray and CT scan revealed a well enhancing soft tissue tumor with a round skull defect and sclerotic margin. The tumor was totally excised with curettage of the skull defect followed by cranioplasty. Pathology was confirmed to be a solitary infantile myofibromatosis. We report this rare solitary infantile myofibromatosis of the temporal bone with review of the pertinent literature.

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