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胎儿上颌寄生胎导致新生儿致命性气道阻塞

Epignathus Leading to Fatal Airway Obstruction in a Neonate.

作者信息

Jadhav Shruti Sudhir, Korday Charusheela Sujit, Malik Sushma, Shah Vivek Kishor, Lad Shilpa Kapil

机构信息

Ex-Assistant Professor, Neonatology Division, Department of Pediatrics, TN Medical College and BYL Nair Hospital , Mumbai, Maharashtra, India .

Ex-Associate Professor, Neonatology Division, Department of Pediatrics, TN Medical College and BYL Nair Hospital , Mumbai, Maharashtra, India .

出版信息

J Clin Diagn Res. 2017 Jan;11(1):SD04-SD05. doi: 10.7860/JCDR/2017/24956.9283. Epub 2017 Jan 1.

Abstract

Teratomas are benign tumours containing cells from ectodermal, mesodermal and endodermal layers with an incidence of about 1 in every 4,000 births. Their commonest site is sacro-coccygeal region, followed by anterior mediastinum. The incidence of teratomas localised to the head and neck region is around 2-9% of all cases. Epignathus is a rare congenital oropharyngeal teratoma originating from the base of the skull. Here we present a rare case of oropharyngeal teratoma in a neonate who was referred to our institute with an ill-defined oral mass protruding through a cleft in the hard palate. Computed tomography scan showed a contrast-enhanced solid mass with areas of calcification and fat extending to oropharynx and nasal cavity with hard palate defect suggestive of a teratoma. Unfortunately, the patient succumbed due to respiratory compromise before the biopsy could be done. Postmortem histopathological examination confirmed diagnosis of benign teratoma consisting of mature tissue.

摘要

畸胎瘤是一种良性肿瘤,包含来自外胚层、中胚层和内胚层的细胞,发病率约为每4000例出生中有1例。其最常见的部位是骶尾部,其次是前纵隔。局限于头颈部区域的畸胎瘤发病率约占所有病例的2-9%。口鼻部畸胎瘤是一种罕见的先天性口咽畸胎瘤,起源于颅底。在此,我们报告一例新生儿口咽畸胎瘤的罕见病例,该新生儿因硬腭裂隙处突出的边界不清的口腔肿物被转诊至我院。计算机断层扫描显示一个增强造影的实性肿物,伴有钙化和脂肪区域,延伸至口咽和鼻腔,硬腭缺损,提示为畸胎瘤。不幸的是,患者在进行活检前因呼吸功能不全死亡。尸检组织病理学检查确诊为成熟组织构成的良性畸胎瘤。

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