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胰腺及腹膜后浆细胞瘤的检测有助于诊断多发性骨髓瘤:一例报告

The Detection of Pancreatic and Retroperitoneal Plasmacytoma Helped to Diagnose Multiple Myeloma: A Case Report.

作者信息

Utsumi Tatsuya, Sasajima Junpei, Goto Takuma, Fujibayashi Shugo, Dokoshi Tatsuya, Sakatani Aki, Tanaka Kazuyuki, Nomura Yoshiki, Ueno Nobuhiro, Kashima Shin, Inaba Yuhei, Inamura Junki, Shindo Motohiro, Moriichi Kentaro, Fujiya Mikihiro, Kohgo Yutaka

机构信息

From the Division of Gastroenterology and Hematology/Oncology, Department of Medicine, Asahikawa Medical University, Asahikawa, Hokkaido, Japan.

出版信息

Medicine (Baltimore). 2015 Jul;94(27):e914. doi: 10.1097/MD.0000000000000914.

Abstract

Multiple myeloma is characterized by the neoplastic proliferation of a single clone of plasma cells producing a monoclonal protein. However, the involvement of pancreas is a rare event. We herein report a rare case of pancreatic plasmacytoma, which was detected before the diagnosis of multiple myeloma.An 83-year-old male was referred to our hospital for further evaluation of obstructive jaundice and a pancreatic mass. A contrast-enhanced computed tomography (CT) scan revealed solid masses with homogenous enhancement in the pancreatic head and retroperitoneum. The histological findings of the retroperitoneal mass obtained by CT-guided biopsy showed multiple sheets of atypical plasma cells, which were positively immunostained for CD79a, CD138, and the κ light chain. Serum immunoelectrophoresis detected M-component of immunoglobulin A-κ, and the histological findings of the bone marrow revealed an abnormally increased number of atypical plasma cells with irregular nuclei and cytoplasmic vacuolation. The patient was therefore diagnosed to have multiple myeloma involving the pancreas and retroperitoneum. Although chemotherapy was performed, the patient died 6 months after the diagnosis.The pancreatic plasmacytoma was detected before the multiple myeloma in the present case. It is difficult to diagnose a pancreatic plasmacytoma without a history of multiple myeloma and related disease.

摘要

多发性骨髓瘤的特征是产生单克隆蛋白的单个浆细胞克隆的肿瘤性增殖。然而,胰腺受累是一种罕见情况。我们在此报告一例罕见的胰腺浆细胞瘤病例,该病例在多发性骨髓瘤诊断之前被检测到。一名83岁男性因阻塞性黄疸和胰腺肿块被转诊至我院作进一步评估。增强计算机断层扫描(CT)显示胰头和腹膜后有均匀强化的实性肿块。CT引导下活检获取的腹膜后肿块组织学检查发现有多片非典型浆细胞,其CD79a、CD138和κ轻链免疫染色呈阳性。血清免疫电泳检测到免疫球蛋白A-κ的M成分,骨髓组织学检查发现非典型浆细胞数量异常增加,细胞核不规则,细胞质有空泡形成。因此,该患者被诊断为多发性骨髓瘤累及胰腺和腹膜后。尽管进行了化疗,但患者在诊断后6个月死亡。在本病例中,胰腺浆细胞瘤在多发性骨髓瘤之前被检测到。没有多发性骨髓瘤及相关疾病病史的情况下,很难诊断胰腺浆细胞瘤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6104/4603181/08ad0dddabfb/medi-94-e0914-g001.jpg

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