RECURRING INFANTILE DIGITAL FIBROMATOSIS - REPORT OF 2 CASES

被引:15
作者
AZAM, SH [1 ]
NICHOLAS, JL [1 ]
机构
[1] HULL ROYAL INFIRM,DEPT PAEDIAT SURG,KINGSTON HULL HU3 2JZ,N HUMBERSIDE,ENGLAND
关键词
INFANTILE FIBROMATOSIS; RECURRING DIGITAL;
D O I
10.1016/0022-3468(95)90617-7
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
There have been 100 reported cases resembling this rare entity. This type of fibroma differs from others in three respects: (1) clinically it is limited to the fingers and toes in infants, (2) it has a remarkable tendency to recur, and (3) morphologically it is characterized by the presence of cytoplasmic inclusion bodies. Herein the authors discuss two cases. This type of fibroma appears from birth to age 3 years in the digits; if correctly diagnosed and left alone, it will regress spontaneously. On the basis of the literature, the present cases were treated conservatively and had follow-up until the fibromas disappeared and did not recur. Copyright (C) 1995 by W.B. Saunders Company
引用
收藏
页码:89 / 90
页数:2
相关论文
共 7 条
[1]  
BECKETT JH, 1977, PEDIATRICS, V3, P401
[2]  
BLOEM JJ, 1974, J BONE JOINT SURG BR, V4, P746
[3]   RECURRING DIGITAL FIBROUS TUMOR OF CHILDHOOD - CASE-REPORT WITH LONG-TERM FOLLOW-UP AND REVIEW OF THE LITERATURE [J].
DABNEY, KW ;
MACEWEN, GD ;
DAVIS, NE .
JOURNAL OF PEDIATRIC ORTHOPAEDICS, 1986, 6 (05) :612-617
[4]  
ENZINGER FM, 1988, SOFT TISSUE TUMORS, P168
[5]  
GRUNNET N, 1973, ACTA PATH MICRO IM A, VA 81, P167
[6]   IS THERE A PLACE FOR CHEMOTHERAPY IN THE MANAGEMENT OF RECURRENT DIGITAL FIBROUS TUMOR OF CHILDHOOD - A CASE-REPORT [J].
MATTOT, M ;
NINANE, J ;
CORNU, G ;
DENAYER, P .
PEDIATRIC HEMATOLOGY AND ONCOLOGY, 1989, 6 (01) :27-30
[7]  
REYE RDK, 1965, ARCH PATHOL, V80, P228