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首页> 外文期刊>Journal of neurosurgery. Pediatrics. >Lumbar lipomyelomeningocele and sacrococcygeal teratoma in siblings: Support for an alternative theory of spinal teratoma formation - Report of 2 cases
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Lumbar lipomyelomeningocele and sacrococcygeal teratoma in siblings: Support for an alternative theory of spinal teratoma formation - Report of 2 cases

机译:兄弟姐妹中的腰部脂膜脑膜膨出和cele尾畸胎瘤:支持脊柱畸胎瘤形成的另一种理论-2例报告

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摘要

Sacrococcygeal teratomas may arise in association with regional developmental errors affecting the caudal embryonic segments and may originate within lumbosacral lipomas. It is therefore possible that sacrococcygeal teratomas and lumbosacral lipomas represent related disorders of embryogenesis. Accordingly, the authors report the cases of 2 siblings. The first child (female) was born with a mature Altman Type III sacrococcygeal teratoma that was resected when she was a neonate. Subsequently, a younger brother was found soon after birth to have an L-4-level lipomyelomeningocele and underwent partial resection and spinal cord untethering at 4 months of age. Although familial forms of each of these conditions have been reported, this is, to the authors' knowledge, the first reported occurrence of lipomyelomeningocele and sacrococcygeal teratoma in siblings. They propose that an inherited regional tendency to developmental error affecting the caudal embryonic segments was shared by these siblings and resulted in spinal teratoma formation in one of them.
机译:cro尾畸胎瘤可能与影响尾状胚胎节段的区域发育错误有关,并可能起源于腰s部脂肪瘤。因此sa球畸胎瘤和腰s部脂肪瘤可能代表了相关的胚胎发生疾病。因此,作者报告了两个兄弟姐妹的病例。第一个孩子(女)出生时患有成熟的奥特曼III型sa尾畸胎瘤,在新生儿时就被切除了。随后,一个弟弟出生后不久被发现患有L-4级脂肪囊膜脑膜膨出症,并在4个月大时接受了部分切除和脊髓束缚。尽管已经报道了每种情况的家族形式,但据作者所知,这是兄弟姐妹中首次报道脂膜膜脑膜膨出和sa尾畸胎瘤。他们提出,这些兄弟姐妹共有遗传性区域发育错误,影响了尾部胚胎节段,并导致其中之一出现了脊柱畸胎瘤。

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