首页> 外文期刊>Journal of the Pancreas >Undifferentiated (Anaplastic) Carcinoma of the Pancreas with Osteoclast-Like Giant Cells Showing Various Degree of Pancreas Duct Involvement. A Case Report and Literature Review
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Undifferentiated (Anaplastic) Carcinoma of the Pancreas with Osteoclast-Like Giant Cells Showing Various Degree of Pancreas Duct Involvement. A Case Report and Literature Review

机译:胰腺未分化(变性)癌,具有破骨细胞样巨细胞,显示不同程度的胰腺导管受累。病例报告及文献复习

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Context Undifferentiated (anaplastic) carcinomaof the pancreas with osteoclast-like giant cells is exceedingly rare. The prognosisof undifferentiated carcinoma is worse than that of poorly differentiated ductaladenocarcinoma of the pancreas; however, undifferentiated carcinoma with osteoclast-likegiant cells might have a more favorable prognosis. Case report We reportthe case of undifferentiated carcinoma of the pancreas with osteoclast-like giantcells, showing an intraductal growth pattern with various degree of pancreas ductinvolvement in the different areas. As a result, we were able to demonstrate theentire spectrum of changes, ranging from the early, minimal intraluminal growthto the partial or complete occlusion of the branches of the main pancreatic duct,and finally invasion and formation of the large necrotic/degenerated cysts. ConclusionsOur findings support the epithelial origin of undifferentiated carcinoma of thepancreas with osteoclast-like giant cells. In early stages, the affected pancreaticduct epithelium was intermingled with nonepithelial component and had an immunoprofiledistinctive from the epithelial lining of the uninvolved (normal) pancreatic ducts.Distinctive immunoprofile (CK 5/6, p63 and p53 positive) of the epithelial componentand p63 and p53 positivity of the nonepithelial component should be explained andfurther investigated in the similar cases. Our findings support prior assertionsthat undifferentiated carcinoma of the pancreas with osteoclast-like giant cellsmay develop from carcinoma in situ within the main pancreatic duct or its branches.
机译:背景破骨细胞样巨细胞胰腺未分化(变性)癌极为罕见。未分化癌的预后要好于胰腺低分化导管腺癌的预后。然而,具有破骨细胞样细胞的未分化癌的预后可能更好。病例报告我们报道了破骨细胞样巨细胞未分化的胰腺癌病例,显示了不同区域内胰管受累程度不同的导管内生长模式。结果,我们能够证明整个变化范围,从早期,最小的腔内生长到主要或胰管分支的部分或完全闭塞,最后是大坏死/变性囊肿的侵入和形成。结论我们的发现支持破骨细胞样巨细胞胰腺未分化癌的上皮起源。在早期阶段,受影响的胰管上皮与非上皮成分混合在一起,其免疫谱与未受累(正常)胰管的上皮内膜区分开。上皮成分与p63和p53的独特免疫谱(CK 5/6,p63和p53阳性)在类似情况下,应解释并进一步研究非上皮成分的阳性。我们的发现支持先前的断言,即具有破骨细胞样巨细胞的胰腺未分化癌可能是从主胰管或其分支内原位癌发展而来的。

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