Authors: K. Jarošová; J. Hoza 1; D. Němcová 1; F. Charvát 2 Authors‘ workplace: Revmatologický ústav, Praha, ředitel doc. MUDr. K. Pavelka, CSc. 1 Klinika dětského a dorostového lékařství UK, Praha, přednosta doc. MUDr. J. Hoza, CSc. 2 Radiodiagnostické oddělení ÚVN Praha, přednosta prim. MUDr. P. Fencl, CSc. Published in: Čes. Revmatol., , 1999, No. 3, p. 138-141. Category:
The authors describe a patient with the polyarticular form of pigmented villonodular synovitisassociated with many inborn phenotypic abnormalities. The presence of these signs, typical for theNoonan syndrome and the histological finding of giant cells in synovial biopsy are described asNoonan-like/multiple giant cell syndrome.
Key words: polyarticular form of pigmented villonodular synovitis, Noonan-like/multiple giantcell syndrome, radiotherapy
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