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neonatal gastric perforation: A single center experience

World Journal of Gastrointestinal Surgery 2014年第8期6卷 151-155页

作者： Jeik Byun h.un young Kim Seung Yeon noh Soo hong Kim Sung Eun Jung Seong Cheol Lee Kwi Won Park Department of Pediatric Surgery Seoul National University Children’s Hospital

AIM: To determine the etiology and prognostic factors for neonatal gastric perforation(nGP), a rare but life-threatening ***: Between 1980 and 2011, nine patients un-derwent surgical intervention for nGP at Seoul national university Children's hospital. The characteristics and prognosis of the patients were retrospectively ***: Among the nine patients, three(33.3%) were preterm babies and five(55.5%) had associated anomalies, which included diaphragmatic eventration(n = 2), congenital diaphragmatic hernia, esophageal atresia with tracheoesophageal fistula, and antral web. Three(33.3%) patients were born before 1990 and three(33.3%) had a birth weight neumo-peritoneum was found on preoperative images in six(66.7%) patients, and incidentally in the other three(33.3%) patients. Surgery was performed within 24 h after the onset of symptoms in seven(77.8%) patients. The overall mortality rate was 22.2%(2/9). The time between symptoms and surgical intervention was the only prognostic factor for survival, whereas premature birth and birth weight were ***: Early detection and advances in neo-natal intensive care may improve the prognosis of nGP.

关键词： neonate Gastric perforation Etiology Prognosis Surgical intervention

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PSP样脑和脊髓nFT-tau病理表现的青年发病的肢体痉挛

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世界核心医学期刊文摘（神经病学分册） 2005年第8期1卷 54-54页

作者： Papapetropoulos S. Scaravilli T. Morris h. F.Scaravilli 张玉龙 Department of Molecular neuroscience Divisionof Neuropathology Institute of Neurology QueenSquare London WC1N 3 BG United Kingdom Dr.

A 30-year-old white man presented with a sporadic form of gradually progress ive spastic gait and, later, supranuclear vertical and horizontal gaze palsy, mi ld cognitive impairment, loss of postural reflexes, and falls. DnA analysis reve aled h1/h1 haplotype without tau gene (exons 9 to 13) mutation. Eight years late r, postmortem revealed a tauopathy similar to progressive supranuclear palsy. un usual aspects were early age at onset, neurofibrillary tangle, and tau involveme nt of the cord.

关键词： nFT-tau PSP 样脑肢体痉挛凝视麻痹痉挛步态神经纤维缠结姿势反射发病年龄 DnA

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