소아형(유건종양)섬유종증
A Case of Infantile(desmoid-type)Fibromatosis
대한암학회지 1994년 26권 4호 p.670 ~ 676
정현식, 장상근,
소속 상세정보
정현식 ( )
건국대학교
장상근 ( )
건국대학교
KMID : 0360319940260040670
Abstract
Infantile(desmoid-type) fibromatosis, which represents the childhood counterpart of musculoaponeurotic fibromatosis(abdominal or extra-abdominal desmoid), usually arises as a solitary mass in skeletal muscle or in the adjacent fascia,
aponeurosis,
or
periosteum. It chiefly affects children from birth to 5 years of age and shows considerable variations in its morphological appearance that range from primitive mesenchymal forms to lesions that closely resemble adult desmoids except for the less
uniform pattern and greater degree of cellularity. This tumor is a rare benign, but potentially locally aggresive lesion that is best treated by wide local resection. It has been confused with congenital fibrosarcoma and other soft tissue
malignant
tumors. One case of infantile fibromatosis affecting left gluteal region is reported.
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