Omrani H, Hui Bon Hoa I, Bennis H, Lehmann M, Zerr V
Service de gynécologie, hôpital d'Haguenau, université de Strasbourg, 64, avenue du Professeur-René-Leriche, 67504 Haguenau cedex, France.
J Gynecol Obstet Biol Reprod (Paris). 2010 Nov;39(7):584-7. doi: 10.1016/j.jgyn.2010.05.010. Epub 2010 Jul 4.
Gorlin syndrome also known as basal cell nevus syndrome is a rare autosomal dominant condition with variable expression. This syndrome is characterized by many anomalies of development and by the propensity of developing multiple neoplasms. We report a case of a 20-years-old French patient who has relapsing ovarian bilateral fibromas in condition of Gorlin syndrome. These fibromas are present in 25 % of Gorlin syndrome cases, which often are bilateral. The economic resection of these fibromas is recommended in spite of the risk of recurrence to preserve the fertility.
戈林综合征也称为基底细胞痣综合征,是一种罕见的常染色体显性遗传病,表现多样。该综合征的特征是存在多种发育异常以及易患多种肿瘤。我们报告一例20岁的法国患者,患有戈林综合征,双侧卵巢纤维瘤复发。这些纤维瘤在25%的戈林综合征病例中出现,且常为双侧性。尽管有复发风险,但为保留生育能力,建议对这些纤维瘤进行经济有效的切除。