首页> 外文期刊>Autopsy & case reports. >A pancreatic mixed neuroendocrine-non-neuroendocrine neoplasms (MiNEN) (NET and undifferentiated carcinoma of the pancreas with osteoclast-like giant cells) with metastatic neuroendocrine component to the liver
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A pancreatic mixed neuroendocrine-non-neuroendocrine neoplasms (MiNEN) (NET and undifferentiated carcinoma of the pancreas with osteoclast-like giant cells) with metastatic neuroendocrine component to the liver

机译:一种胰腺混合神经内分泌 - 非神经内分泌肿瘤(Minen)(胰腺与骨质蛋白样巨细胞的胰腺癌和未分化的癌),肝脏转移神经内分泌成分

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Undifferentiated carcinoma of the pancreas with osteoclast-like giant cells (UCOGCs) is an extremely rare morphologically and clinically distinct variant of pancreatic ductal adenocarcinoma (PDAC), exhibiting a characteristic component of reactive osteoclast-like giant cells admixed with neoplastic mononuclear cells. Sommers and Meissner first described it in 1954 as an “unusual carcinoma of the pancreas”. Later it acquired many different names. In 2010, the WHO classified these tumors as a variant of PDAC under the heading of “undifferentiated carcinoma with osteoclast-like giant cells”. Here we describe the first case of pancreatic mixed neuroendocrine-non-neuroendocrine neoplasms (MiNEN) composed of UCOGC and pancreatic neuroendocrine tumor (NET), which occurred in a 78-year-old man with biliary colic and pancreatitis. The mass did not respond to the chemotherapy, and he soon developed liver metastasis from the NET component, and unfortunately, the patient passed away 10 months later. Since UCOGC is extremely rare, and its association with NET has not been reported yet, our case expands the knowledge regarding its unusual presentation and poor prognosis.
机译:胰腺样胰腺样巨细胞(UcoGC)的胰腺的未分化癌是一种极其罕见的形​​态学和胰腺导管腺癌(PDAC)的临床上不同的变体,其表现出与肿瘤单核细胞混合的反应性破骨细胞样巨细胞的特征组分。 Sommers和Meissner首先将1954年描述为“胰腺的异常癌”。后来它获得了许多不同的名称。在2010年,将这些肿瘤分类为PDAC的变体,该肿瘤在“未分化的癌巨型细胞的未分化癌”中的含量。在这里,我们描述了由UcoGC和胰腺神经内分泌肿瘤(网)组成的第一种胰腺混合神经内分泌 - 非神经内分泌肿瘤(Minen)的案例,该胰腺神经内分泌肿瘤(净)发生在一名78岁的患有胆道和胰腺炎的78岁男性中。质量没有响应化疗,并且很快就开始了来自网组件的肝脏转移,不幸的是,患者在10个月后通过了。由于Ucogc非常罕见,尚未报告其与网的关联尚未报告,我们的案例扩大了有关其不寻常呈现和预后不良的知识。

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