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[Association of ovarian juvenile granulosa cell tumor with Maffucci's syndrome]. 2002
H Hachi, and
A Othmany, and
A Douayri, and
C Bouchikhi, and
F Tijami, and
L Laâlou, and
M Chami, and
A Boughtab, and
A Jalil, and
S Benjelloun, and
F Ahyoud, and
F Kettani, and
A Souadka
Service de chirurgie carcinologique, institut national d'oncologie Sidi Mohamed Ben Abdellah, Rabat, Maroc. hafidhachi@hotmail.com
The authors report a rare case of the ovarian juvenile granulosa cell tumor associated with Maffucci's syndrome (enchondromathosis + hemangiomas), no heriditary mesodermal dysplasia. Sarcomatous changes of chondromas are encountered most frequently; however other various typed neoplasma have been reported: ovarian juvenile granulosa cell tumor may occur not infrequently in female patients with Maffucci's syndrome in the first or second decades. Sarcomatous changes of choromas established prognosis of the Maffucci's syndrome.
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