Shipp T D, Bromley B, Benacerraf B
Department of Obstetrics and Gynecology, Brigham and Women's Hospital, Boston, MA, USA.
J Ultrasound Med. 1995 Sep;14(9):673-8. doi: 10.7863/jum.1995.14.9.673.
Our objective was to determine the appearance, cause, and outcome of fetal face masses diagnosed antenatally by ultrasonography. Over a 6 year period, 10 consecutive fetuses with facial masses were identified. Ultrasonographic findings, neonatal pathologic findings, and outcome data were correlated. Four (40%) of the 10 fetuses died, including one with a palatal teratoma associated with a Dandy-Walker malformation and three with intracranial teratomas--one of which was associated with hydrops fetalis. Among the survivors, one fetus had a dacryocystocele that was managed conservatively and one had drainage of a salivary gland cyst. The remaining four neonates had successful excision of their tumors in the neonatal period and survived; these infants had a nasal teratoma, a thyroid teratoma, a gingival granular cell tumor, and a scalp hemangioma. Four of the 10 pregnancies had associated polyhydramnios, three of which ended in stillbirth or neonatal death. In conclusion, 40% of the fetuses with antenatal diagnosis of fetal facial masses did not survive. If those with intracranial teratomas are removed from this group, one of seven (14%) fetuses with extracranial masses died. The intracranial teratomas were uniformly fatal. Polyhydramnios was associated with poor outcome.
我们的目的是确定产前通过超声诊断的胎儿面部肿块的表现、病因及结局。在6年期间,连续发现10例有面部肿块的胎儿。对超声检查结果、新生儿病理检查结果及结局数据进行了关联分析。10例胎儿中有4例(40%)死亡,其中1例患有与丹迪-沃克畸形相关的腭部畸胎瘤,3例患有颅内畸胎瘤,其中1例合并胎儿水肿。在存活者中,1例胎儿患有泪囊膨出,采用保守治疗,1例唾液腺囊肿进行了引流。其余4例新生儿在新生儿期成功切除肿瘤并存活;这些婴儿分别患有鼻畸胎瘤、甲状腺畸胎瘤、牙龈颗粒细胞瘤和头皮血管瘤。10例妊娠中有4例合并羊水过多,其中3例以死产或新生儿死亡告终。总之,产前诊断为胎儿面部肿块的胎儿中,40%未能存活。如果将患有颅内畸胎瘤的胎儿排除在该组之外,7例患有颅外肿块的胎儿中有1例(14%)死亡。颅内畸胎瘤均为致命性。羊水过多与不良结局相关。