胎儿

Q4 Medicine
S. Malwade, S. Mane, Nanigiri Sneha, S. Agarkhedkar
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引用次数: 0

摘要

胎儿是在 19 世纪初由梅克尔首次发现的。这是一种罕见的先天性畸形,由异常胚胎发育引起,在正常发育的宿主体内发现一个畸形的寄生双胞胎。在大多数情况下,寄生孪生子是无脑儿,通常有脊椎和出芽的四肢。上肢发育不如下肢,通常位于自体的腹部。通常在术前通过超声波检查、普通放射线检查、计算机断层扫描或磁共振成像进行诊断。组织病理学检查结果可确诊,建议的治疗方法是手术切除肿块。我们报告了一例 15 个月大的尼泊尔裔男婴的病例,他在新生儿期被诊断为腹部肿块,并转诊至我院。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Fetus in fetu
Fetus in fetu was first identified in the early 19th century by Meckel. It is a rare congenital anomaly which occurs from anomalous embryogenesis in which a malformed parasitic twin is found within the body of the normally developed host. In most cases, the parasitic twin is anencephalic and usually contains a vertebral column and budding limbs. The upper limbs are less developed than lower limbs, and are usually located in the abdomen of the autosite. Diagnosis is often made preoperatively with ultrasonography, plain radiography, computed tomography, or magnetic resonance imaging. Histopathological findings confirm the diagnosis and the recommended treatment is complete surgical excision of mass. We report a case of 15-month-old baby boy of Nepalese origin referred to our hospital with mass in abdomen diagnosed during neonatal period.
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来源期刊
CiteScore
0.30
自引率
0.00%
发文量
221
审稿时长
43 weeks
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