Fibroblastic rheumatism is a rare entity. Nineteen cases were reported in t
he literature, and among them, only one in a child.
Case report. - Cam. (born August 19, 1988) had an onset of disease in Octob
er 1996 with nodules on the MCP and PIP: elbows and tibia, with partial imp
rovement after three months. In April 1997, she suffered from arthralgia an
d stiffness of both wrists, and then of the big toes. X-rays showed destruc
tive and erosive lesions on both wrists and on the PIP of the second and th
ird fingers and the big foes. Laboratory investigations disclosed normal va
lues for ESR and CRP and negative results for ANA and RF: The diagnosis of
fibroblastic rheumatism was based on the typical histologic pattern of a no
dule. The treatment associated colchicin and rehabilitation. In August 1998
, the wrists' stiffness began to improve, though the big toes remained tota
lly stiff. The radiologic erosive lesions did not show progress.
Comments. - The diagnosis of fibroblastic rheumatism is based on the histol
ogic pattern of the nodules. The erosive evolution of the arthropathies is
infrequent (8/15 cases in adults). Juvenile onset is very rare; only one ca
se has been reported, in a 10-year-old boy. The mechanism of the disease re
mains unknown. As it is very rare, the therapeutic strategies are not well
established.
Conclusion. - This disease should be considered among the causes of juvenil
e arthritis with erosion. (C) 2001 Editions scientifiques et medicales Else
vier SAS.