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胰腺导管腺癌和神经内分泌瘤碰撞瘤——罕见病例报告。

Pancreatic collision tumor of ductal adenocarcinoma and neuroendocrine tumor-A rare case report.

机构信息

Department of Pathology, Kalinga Institute of Medical Sciences, Bhubaneswar, Odisha, India.

Department of Surgical Gastroenterology, Kalinga Institute of Medical Sciences, Bhubaneswar, Odisha, India.

出版信息

Indian J Pathol Microbiol. 2021 Jun;64(Supplement):S172-S174. doi: 10.4103/IJPM.IJPM_735_19.

Abstract

A collision tumor is composed of two adjacent histological distinct neoplasms without the histological admixture of cell types in the same organ or tissue. It is rare in pancreas. Herein we report an unusual case of a mixed malignant neuroendocrine tumor (NET) and ductal adenocarcinoma of pancreas in a 24 year old male who presented with history abdomen pain. A clinicoradiological diagnosis of chronic calcific pancreatitis with carcinoma body of pancreas was made. Distal pancreaticosplenectomy specimen showed a grey white, nodular growth measuring 2 x 2 x 1.2 cm on the cut surface of pancreas. Histopathology revealed a composite tumor consisting of ductal and neuroendocrine origin. Immunohistochemistry showed complementary staining for CK7 in adenocarcinoma and chromogranin A in NET areas confirming a collision tumor. Accurate evaluation of the radiologic pointers, histomorphologic evaluation to recognize and quantitate the individual components, appropriate immunohistochemical evaluation and correlation is essential for diagnosis.

摘要

碰撞瘤由两个相邻的组织学上截然不同的肿瘤组成,而同一器官或组织中没有细胞类型的组织学混合。它在胰腺中很少见。在此,我们报告一例罕见的 24 岁男性胰腺混合性恶性神经内分泌肿瘤(NET)和导管腺癌病例,该患者有腹痛病史。临床放射学诊断为慢性钙化性胰腺炎伴胰体部癌。远端胰脾切除术标本显示胰腺切面有灰白色、结节状生长,大小为 2x2x1.2cm。组织病理学显示由导管和神经内分泌起源组成的复合肿瘤。免疫组织化学显示腺癌中 CK7 的互补染色和 NET 区域中嗜铬粒蛋白 A 的染色,证实为碰撞瘤。准确评估放射学指标、识别和量化单个成分的组织形态学评估、适当的免疫组织化学评估和相关性对于诊断至关重要。

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