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食管导管内乳头状黏液性肿瘤:一例罕见的吞咽困难病例。

Intraductal papillary mucinous neoplasm of the oesophagus: an unusual case of dysphagia.

作者信息

Crighton E, Botha A

机构信息

Guy's and St Thomas' NHS Foundation Trust, London, UK.

出版信息

Ann R Coll Surg Engl. 2012 Mar;94(2):e92-4. doi: 10.1308/003588412X13171221589090.

Abstract

We report the case of a 58-year-old woman presenting with dysphagia secondary to an intraductal papillary mucinous neoplasm arising from a heterotopic pancreas in the oesophageal wall. This was successfully treated with a laparoscopic/thoracoscopic ivor Lewis oesophagectomy. Dysphagia is the most common symptom of oesophageal tumours regardless of aetiology of the tumour and can be treated successfully with surgical resection. Through an extensive search of the literature, we found that a heterotopic pancreas in the oesophagus is extremely rare with only ten cases being reported. We describe what we believe to be the first case of a heterotopic pancreas in the oesophagus transforming into an intraductal papillary mucinous neoplasm.

摘要

我们报告了一例58岁女性病例,该患者因食管壁异位胰腺发生导管内乳头状黏液性肿瘤继发吞咽困难。通过腹腔镜/胸腔镜下艾弗·刘易斯食管切除术成功治疗了该疾病。无论肿瘤病因如何,吞咽困难都是食管肿瘤最常见的症状,手术切除可成功治疗。通过广泛检索文献,我们发现食管异位胰腺极为罕见,仅报道过10例。我们描述了我们认为是第一例食管异位胰腺转变为导管内乳头状黏液性肿瘤的病例。

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