产前突出眼显示出生后眼眶畸胎瘤。

IF 0.7 Q4 OPHTHALMOLOGY
Case Reports in Ophthalmological Medicine Pub Date : 2020-07-13 eCollection Date: 2020-01-01 DOI:10.1155/2020/1597353
Ahgbatouhabeba Ahnoux-Zabsonre, Jérôme Sanou, Yérénou Ferdinand Lankoandé, Chantal Bouda, Gertrude Méda, Assita Lamien-Sanou
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引用次数: 2

摘要

目的:畸胎瘤是由三胚层干细胞形成的先天性肿瘤。它们通常位于骶尾骨区。眼眶畸胎瘤是罕见的,截至2016年报告的病例不到70例。我们报告的情况下,产前突出眼发现超声检查,原来是一个畸胎瘤出生后。正如文献中所描述的那样,我们病例中的新生儿是女性。治疗包括完全切除畸胎瘤和眼球。由于我们的医疗技术有限,重建手术仍然是一个巨大的挑战。结论:胎儿超声检查出的产前突出眼,即使非常罕见,也应使我们想到畸胎瘤。胎儿眼眶畸胎瘤可能与胎儿存活率有关。婴儿将受益于眼眶重建手术。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Prenatal Exophthalmia Revealing a Postnatal Orbital Teratoma.

Prenatal Exophthalmia Revealing a Postnatal Orbital Teratoma.

Prenatal Exophthalmia Revealing a Postnatal Orbital Teratoma.

Prenatal Exophthalmia Revealing a Postnatal Orbital Teratoma.

Purpose: Teratomas are congenital tumors of stem cells derived from the three germ layers. They are frequently located in the sacrococcygeal region. Orbital teratoma is rare with less than 70 cases reported until 2016. We report the case of prenatal exophthalmia discovered by ultrasound exam which turned out to be a teratoma postnatally. The newborn in our case was female, just as described in the literature. Treatment consisted of total removal of the teratoma and the eyeball. Reconstructive surgery remains a big challenge since our medical technology is limited.

Conclusion: A prenatal exophthalmia on fetal ultrasound should make us think of a teratoma, even if it is very rare. Fetal orbital teratoma may be associated with fetal survival. The infant will benefit from a reconstructive surgery of the orbit.

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