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Arch Gynecol Obstet ; 285(3): 879-82, 2012 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-22037684

RESUMEN

PURPOSE: To report the first case of fertility treatment in a patient with May-Hegglin anomaly, a rare hematological disorder inherited as an autosomal dominant trait. METHOD: We present a case report of a 40-year-old nulliparous patient with May-Hegglin anomaly who underwent her first ICSI cycle with transfer of three fresh embryos. RESULTS: Prophylactic platelet transfusion obtained by single-donor apheresis was performed 1 h before the oocyte pick up. No complications were reported. No pregnancy was obtained. CONCLUSIONS: We report about the possibility to assist women affected by May-Hegglin anomaly requiring reproductive assistance. However, a multidisciplinary team composed of gynecologists and hematologists should follow such patients carefully, in order to carry out a complete clinical evaluation and to prevent the potential risks of bleeding. Clinicians must be vigilant in their presentation of risks, benefits, and alternatives.


Asunto(s)
Transferencia de Embrión , Infertilidad Femenina/terapia , Trombocitopenia/complicaciones , Adulto , Femenino , Pérdida Auditiva Sensorineural , Humanos , Transfusión de Plaquetas
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