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ABSTRACT Objective
Beyond the classic triad of peripheral precocious puberty, café‐au‐lait skin pigmentation and polyostotic fibrous dysplasia, partial presentation McCune–Albright syndrome (MAS) has been reported, including the association of isolated recurrent ovarian cysts in early infancy. The aims of this study were to determine whether isolated voluminous fetal unilateral ovarian cysts (diameter > 4 cm) may be associated with a Gsα activating mutation, suggestive of MAS.
DesignWe followed five female fetuses presenting with voluminous unilateral ovarian cysts by ultrasonography until delivery. At birth, all patients underwent percutaneous cyst aspiration and two patients later underwent ovariectomy. A sensitive PCR‐based method was used to analyze the Gsα activating mutation in DNA obtained from ovarian cystic fluids or tissue.
ResultsAmong the five cases, one Gsα mutation (R201C) was identified in the ovarian tissue.
ConclusionsWe demonstrate for the first time that voluminous fetal unilateral ovarian cysts may be suggestive of MAS. Systematic search for the Gsα mutation should be performed in all newborns with voluminous fetal unilateral ovarian cysts requiring percutaneous cyst aspiration, because early diagnosis of MAS prevents unnecessary oophorectomy to eliminate questions of malignancy and imposes long‐term clinical, biological, and imaging follow‐up to detect other early manifestations of MAS. © 2012 John Wiley & Sons, Ltd.
| Authors: | Laura Gaspari, Françoise Paris, Marc Nicolino, Frédéric Hameury, Hélène Bonnaure, Catherine Pienkowski, Nadège Servant, Nicolas Kalfa, Charles Sultan | |
| Journal: | Prenatal Diagnosis | |
| Year: | 2012 | |
| Pages: | 1 | |
| DOI: | 10.1002/pd.3921 | |
| Publication date: | 13-06-2012 |
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