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[意大利无脑儿的流行病学研究及我们所观察病例的解剖病理学发现]

[Epidemiological study of anencephaly in Italy and anatomo-pathological findings in cases observed by us].

作者信息

Abrate M, Baracchini P, Fulcheri E, Lapertosa G, Pantarotto M F, Mastroiacovo P

机构信息

Servizio di anatomia patologica (USSL 61) di Savigliano.

出版信息

Pathologica. 1990 Mar-Apr;82(1078):133-54.

PMID:2392336
Abstract

Epidemiologic study of anencephaly in Italy and anatomo-pathological analysis of our series. Out of about 1,000,000 new-borns enrolled in the IPIMC Register (Italian Multicenter Study on Congenital Malformations) from 1978 to 1986, 205 were found with isolated anencephaly and 59 with anencephaly associated with other independent malformations, for a total of 284 cases. The study of preferentially associated malformations has pointed out that anencephaly is mainly associated with three kinds of malformations: cleft lip and/or palate, ambiguous genitalia, gastroschisis. Yet these combinations did not result to be the most common with spina bifida, thus proving the heterogeneity of these two neural canal defects. The total rate is 2.7 (/10,000), higher in the South (3.2) than in the North (2.3). The highest rate was reported in Sardinia (6.0). Moreover, a 58.1% trend reduction between 1978-80 and 1984-86 with seasonal peak in January (3.6%) was reported. The following major new-born and mother characteristics have been studied: sex (M/F = 0.76), twin pregnancies (6.4%), vitality (live births: 60, from them 40 died in the same day, 16 between day 1 and 7, 4 after day 7 since birth; still births: 47; born with unknown vitality: 10), mother age (no influence), consanguinity (4.4%), average weight (1,891 gr.), mean gestational age (246 days), intrauterine growth retardation (52.9%). The importance of a proper and careful examination during autopsy is stressed to identify and describe possible associated malformations. Immunohistochemical data (4 cases) on the cerebro-vascular area are reported, mainly to identify any neural buds and related structures (glia, neurofilaments, ganglia, nerves, ependyma, choroid plexus) as well as the connection between osteocartilaginous and epithelial and/or vascular rudiments.

摘要

意大利无脑儿的流行病学研究及我们系列病例的解剖病理学分析。在1978年至1986年纳入IPIMC登记册(意大利先天性畸形多中心研究)的约100万新生儿中,发现205例为单纯无脑儿,59例为合并其他独立畸形的无脑儿,共计284例。对优先合并畸形的研究指出,无脑儿主要与三种畸形相关:唇裂和/或腭裂、两性生殖器畸形、腹裂。然而,这些组合并非脊柱裂最常见的情况,从而证明了这两种神经管缺陷的异质性。总发病率为2.7(/10,000),南方(3.2)高于北方(2.3)。撒丁岛报告的发病率最高(6.0)。此外,报告显示1978 - 80年至1984 - 86年期间发病率有58.1%的下降趋势,1月份出现季节性高峰(3.6%)。研究了以下主要的新生儿和母亲特征:性别(男/女 = 0.76)、双胎妊娠(6.4%)、活力(活产:60例,其中40例在同一天死亡,16例在出生后第1天至第7天死亡,4例在出生后第7天以后死亡;死产:47例;出生时活力不明:10例)、母亲年龄(无影响)、近亲结婚(4.4%)、平均体重(1,891克)、平均孕周(246天)、宫内生长迟缓(52.9%)。强调了尸检时进行适当仔细检查以识别和描述可能合并畸形的重要性。报告了脑血管区域的免疫组织化学数据(4例),主要用于识别任何神经芽及相关结构(胶质细胞、神经丝、神经节、神经、室管膜、脉络丛)以及骨软骨与上皮和/或血管原基之间的连接。

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