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表现为先天性肺气道畸形的穿孔性神经肠囊肿

Perforated neuroenteric cyst masquerading as congenital pulmonary airway malformation.

作者信息

Gundapaneni Sreekar, Jain Vishesh, Sharma Shilpa, Gupta Devendra Kumar

机构信息

Department of Pediatric Surgery, All India Institute of Medical Sciences, New Delhi, India.

出版信息

BMJ Case Rep. 2017 Dec 2;2017:bcr-2017-222537. doi: 10.1136/bcr-2017-222537.

Abstract

A 3-month-old child was presented with haemoptysis with respiratory distress. Imaging was suggestive of a cavitary lesion in the lung with surrounding consolidation. Diagnosis of a primary lung pathology like congenital pulmonary airway malformation was considered. Based on clinical suspicion and prior experience, a Tc-99m pertechnetate radionuclide study was performed, which clinched the diagnosis of foregut duplication cyst. Intraoperative findings confirmed the presence of a neuroenteric cyst. The child remains asymptomatic on follow-up awaiting neurosurgical intervention for the intraspinal component of the cyst.

摘要

一名3个月大的儿童出现咯血并伴有呼吸窘迫。影像学检查提示肺部有空洞性病变并伴有周围实变。考虑诊断为先天性肺气道畸形等原发性肺部疾病。基于临床怀疑和既往经验,进行了锝-99m高锝酸盐放射性核素检查,确诊为前肠重复囊肿。术中发现证实存在神经肠囊肿。该患儿在随访中无症状,等待对囊肿脊髓内部分进行神经外科干预。

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