摘要
<strong>Background:</strong><span style="font-family:""><span style="font-family:Verdana;"> Dysgerminoma is a germ cell tumor of the ovary usually found in young women. It represents 1% to 2% of all ovarian cancers. The preoperative</span><span><span style="font-family:Verdana;"> diagnosis is generally difficult. The surgery and the pathology study are therefore essential for the </span><span style="font-family:Verdana;">diagnosis,</span><span style="font-family:Verdana;"> and optimal management. The incidence of pregnancy with dysgerminoma is extremely low. The treatment and management during pregnancy often jeopardize the </span><span style="font-family:Verdana;">materno-fetal</span><span style="font-family:Verdana;"> prognosis. We report a case of ovarian dysgerminoma in an 18-year-old pregnant woman. </span><b><span style="font-family:Verdana;">Observation: </span></b><span style="font-family:Verdana;">Patient</span><span style="font-family:Verdana;"> was an 18-year-old, female with no known past medical history, who presented to the emergency room at 29 weeks + 3 days pregnancy with dyspnea and a voluminous uterus (height 42</span></span></span><span style="font-family:""> </span><span style="font-family:Verdana;">cm). An ultrasound showed an active pregnancy, and a large vascularized, finely echogenic, multi-partitioned, thick-walled liquid ovarian tumor. Ca125 was 231.5</span><span style="font-family:""> </span><span style="font-family:""><span style="font-family:Verdana;">IU/ml. Ovarian dysgerminoma was suspected. The </span><span style="font-family:Verdana;">surgery</span><span style="font-family:Verdana;"> and the pathology study of the surgical specimen confirmed the suspected diagnosis. </span><span style="font-family:Verdana;">Patient</span><span style="font-family:Verdana;"> died on </span><span style="font-family:Verdana;">postoperative</span><span style="font-family:Verdana;"> day 8. </span></span><b><span style="font-family:Verdana;">Conclusion: </span></b><span style="font-family:""><span style="font-family:Verdana;">Ovarian dysgerminoma is a rare malignant tumor, which must be suspected in </span><span style="font-family:Verdana;">case</span><span style="font-family:Verdana;"> of complex ovarian mass of young women. When diagnosed during pregnancy, its management jeopardizes the </span><span style="font-family:Verdana;">materno-foetal</span><span style="font-family:Verdana;"> prognosis.</span></span>
<strong>Background:</strong><span style="font-family:""><span style="font-family:Verdana;"> Dysgerminoma is a germ cell tumor of the ovary usually found in young women. It represents 1% to 2% of all ovarian cancers. The preoperative</span><span><span style="font-family:Verdana;"> diagnosis is generally difficult. The surgery and the pathology study are therefore essential for the </span><span style="font-family:Verdana;">diagnosis,</span><span style="font-family:Verdana;"> and optimal management. The incidence of pregnancy with dysgerminoma is extremely low. The treatment and management during pregnancy often jeopardize the </span><span style="font-family:Verdana;">materno-fetal</span><span style="font-family:Verdana;"> prognosis. We report a case of ovarian dysgerminoma in an 18-year-old pregnant woman. </span><b><span style="font-family:Verdana;">Observation: </span></b><span style="font-family:Verdana;">Patient</span><span style="font-family:Verdana;"> was an 18-year-old, female with no known past medical history, who presented to the emergency room at 29 weeks + 3 days pregnancy with dyspnea and a voluminous uterus (height 42</span></span></span><span style="font-family:""> </span><span style="font-family:Verdana;">cm). An ultrasound showed an active pregnancy, and a large vascularized, finely echogenic, multi-partitioned, thick-walled liquid ovarian tumor. Ca125 was 231.5</span><span style="font-family:""> </span><span style="font-family:""><span style="font-family:Verdana;">IU/ml. Ovarian dysgerminoma was suspected. The </span><span style="font-family:Verdana;">surgery</span><span style="font-family:Verdana;"> and the pathology study of the surgical specimen confirmed the suspected diagnosis. </span><span style="font-family:Verdana;">Patient</span><span style="font-family:Verdana;"> died on </span><span style="font-family:Verdana;">postoperative</span><span style="font-family:Verdana;"> day 8. </span></span><b><span style="font-family:Verdana;">Conclusion: </span></b><span style="font-family:""><span style="font-family:Verdana;">Ovarian dysgerminoma is a rare malignant tumor, which must be suspected in </span><span style="font-family:Verdana;">case</span><span style="font-family:Verdana;"> of complex ovarian mass of young women. When diagnosed during pregnancy, its management jeopardizes the </span><span style="font-family:Verdana;">materno-foetal</span><span style="font-family:Verdana;"> prognosis.</span></span>
作者
Baguilane Douaguibe
Bingo K. M’Bortche
Tina Ayoko Ketevi
Akila Bassowa
Dede Ajavon
T. Dare
Francis Baramna-Bagou
Komi A. Migbegna
Abdoul Samadou Aboubakari
Koffi Akpadza
Baguilane Douaguibe;Bingo K. M’Bortche;Tina Ayoko Ketevi;Akila Bassowa;Dede Ajavon;T. Dare;Francis Baramna-Bagou;Komi A. Migbegna;Abdoul Samadou Aboubakari;Koffi Akpadza(Department of Gynecology and Obstetrics, Sylvanus Olympio University Hospital Center, Lomé, Togo;Togolese Association of Family Well-Being Planning Center (ATBEF), Lome, Togo;Department of Gynecology and Obstetrics, Campus University Hospital Center, Lomé, Togo;Department of Gynecology and Obstetrics, University Hospital Center, Kara, Togo;Department of Pathology, University Teaching Hospital of Lomé, Lomé, Togo)