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伴有双侧外侧裂周围多小脑回畸形及腹部钙化的彼得斯异常。

Peters' anomaly with bilateral perisylvian polymicrogyria and abdominal calcification.

作者信息

Morimoto Mayumi, Takano Tomoyuki, Sakaue Yuko, Sawai Chihiro, Aotani Hirofumi, Koshida Shigeki, Takeuchi Yoshihiro

机构信息

Department of Pediatrics, Shiga University of Medical Science, Seta-Tsukinowa, Otsu, Japan.

出版信息

Congenit Anom (Kyoto). 2004 Jun;44(2):99-102. doi: 10.1111/j.1741-4520.2004.00016.x.

Abstract

We report a neonatal case of Peters' anomaly with bilateral perisylvian polymicrogyria and abdominal calcification. The male infant was born after a normal labor. Bilateral central corneal opacities with iridocorneal strands indicated Peters' anomaly. The X-ray and abdominal computed tomography demonstrated multiple calcifications beneath the diaphragma around the liver and the spleen. TORCH serology was negative. Intracranial calcification was not detected. Brain magnetic resonance imaging demonstrated bilateral perisylvian polymicrogyria. Abdominal calcification was suspected to be related to vascular disruption. Bilateral perisylvian polymicrogyria has been thought to result from ischemic events such as intrauterine hypotension or vascular occlusions. Based on these considerations, we conclude that a vascular disruption sequence may an important pathogenetic mechanism of Peters' anomaly.

摘要

我们报告一例患有双侧外侧裂周围多小脑回畸形和腹部钙化的彼得斯异常新生儿病例。该男婴顺产出生。双侧中央角膜混浊伴虹膜角膜条索提示彼得斯异常。X线和腹部计算机断层扫描显示肝脏和脾脏周围膈肌下方有多处钙化。TORCH血清学检查为阴性。未检测到颅内钙化。脑部磁共振成像显示双侧外侧裂周围多小脑回畸形。腹部钙化被怀疑与血管破坏有关。双侧外侧裂周围多小脑回畸形被认为是由诸如宫内低血压或血管闭塞等缺血事件引起的。基于这些考虑,我们得出结论,血管破坏序列可能是彼得斯异常的一个重要发病机制。

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