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Mucin Hypersecreting Intraductal PapillaryNeoplasm of the Pancreas

机译:粘蛋白分泌过多的导管内乳头胰腺肿瘤

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摘要

Mucin Hypersecreting Intraductal Papillary Neoplasm is a rare neoplasm that arises from ductal epithelial cells. This entity is distinct from the more commonly known Mucinous Cystadenoma or Mucinous Cystadenocarcinoma. Despite this distinction, it has been erroneously categorized with these more common cystic neoplasms. Characteristic clinical presentation, radiographic, and endoscopic findings help distinguish this neoplasm from the cystadenomas and cystadenocarcinomas. Histopathologic identification is not crucial to the preoperative diagnosis. This neoplasm is considered to represent a premalignant condition and, therefore, surgical resection is warranted. Prognosis, following resection, is felt to be curative for the majority of patients.We present two cases of Mucin Hypersecreting Intraductal Papillary Neoplasm and discuss theirdiagnosis and surgical therapy.
机译:粘蛋白分泌过多的导管内乳头状瘤是一种罕见的肿瘤,由导管上皮细胞产生。该实体不同于更普遍已知的粘液性膀胱腺瘤或粘液性膀胱腺癌。尽管有这种区别,但已将其与这些较常见的囊性肿瘤错误地归类。典型的临床表现,影像学检查和内窥镜检查结果有助于将该肿瘤与囊腺瘤和囊腺癌区分开来。组织病理学鉴定对术前诊断并不重要。该肿瘤被认为代表了恶变前的状况,因此,必须进行手术切除。切除后的预后被认为对大多数患者是治愈。我们介绍了两例粘蛋白分泌过多的导管内乳头状瘤患者,并对其进行了讨论。诊断和外科治疗。

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