Donnenfeld A E, Hughes H, Weiner S
Department of Obstetrics and Gynecology, Pennsylvania Hospital, Philadelphia 19107.
Am J Perinatol. 1988 Jan;5(1):51-3. doi: 10.1055/s-2007-999653.
Frontoethmoidal meningoencephaloceles (FEM) are exceedingly rare in the western hemisphere, Australia, and Europe with an estimated frequency of 1 in 40,000 live births. Among the inhabitants of Thailand, Burma, Malaysia, Indonesia, and parts of the Soviet Union, however, the frequency is as high as 1 in 5000, accounting for 15% of all neural tube defects (NTD). Normal maternal serum alpha-fetoprotein (MSAFP) values usually will be found in these cases since most encephaloceles are closed, skin covered defects. Correct interpretation of the sonographic findings is crucial in establishing a diagnosis as well as giving prognostic and recurrence risk information. To our knowledge, this is the first reported case of prenatally diagnosed FEM. Perinatal management, differential diagnosis for disorders associated with this malformation, and epidemiologic information regarding this rare condition are discussed. It is anticipated that the prenatal sonographic findings may be applied to establish this diagnosis in similarly affected fetuses.
额筛部脑膜脑膨出(FEM)在西半球、澳大利亚和欧洲极为罕见,估计活产儿中的发生率为1/40000。然而,在泰国、缅甸、马来西亚、印度尼西亚以及苏联部分地区的居民中,其发生率高达1/5000,占所有神经管缺陷(NTD)的15%。在这些病例中通常会发现母体血清甲胎蛋白(MSAFP)值正常,因为大多数脑膜脑膨出是闭合的、有皮肤覆盖的缺陷。正确解读超声检查结果对于确立诊断以及提供预后和复发风险信息至关重要。据我们所知,这是首例产前诊断为FEM的病例。本文讨论了围产期管理、与这种畸形相关疾病的鉴别诊断以及关于这种罕见病症的流行病学信息。预计产前超声检查结果可用于对类似受影响胎儿进行这种诊断。