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患者输尿管癌腹膜后转移致 Russell 体性十二指肠炎。

Russell body duodenitis in a patient with retroperitoneal metastasis of ureteral cancer.

机构信息

Department of Pathology, Teikyo University School of Medicine, Tokyo 173-8605, Japan.

出版信息

World J Gastroenterol. 2013 Jan 7;19(1):125-8. doi: 10.3748/wjg.v19.i1.125.

Abstract

Russell bodies are globular and eosinophilic inclusion bodies in the cytoplasm of mature plasma cells. Plasma cells whose cytoplasm is filled with Russell bodies are designated as Mott cells. Russell body duodenitis (RBD) is a unique form of chronic duodenitis that is characterized by infiltration of numerous Mott cells. RBD is very rare; only two cases have been reported to date. In this paper, we report a case of RBD in a patient with retroperitoneal metastasis of ureteral cancer. A 77-year-old man was admitted to our hospital complaining of appetite loss, vomiting, and upper abdominal distension. He had undergone left nephroureterectomy for ureteral cancer 4 years earlier. Upper digestive tract endoscopy revealed edema, stenosis, and punctate redness of the mucosa of the duodenum, and a biopsy was performed. Histological analysis showed that numerous Mott cells had infiltrated the lamina propria mucosae, and the condition was diagnosed as RBD. A mass lesion in the retroperitoneum adjacent to the duodenum was detected by abdominal computed tomography, and was diagnosed as metastatic urothelial carcinoma by biopsy. It is possible that chemokines produced by tumor cells caused RBD in this case.

摘要

Russell 小体是成熟浆细胞细胞质中的球形嗜酸性包涵体。细胞质充满 Russell 小体的浆细胞被称为 Mott 细胞。Russell 体性十二指肠炎(RBD)是一种独特的慢性十二指肠炎形式,其特征为大量 Mott 细胞浸润。RBD 非常罕见;迄今为止仅报告了两例。本文报告了一例发生在输尿管癌腹膜后转移患者中的 RBD。一名 77 岁男性因食欲减退、呕吐和上腹胀来我院就诊。他在 4 年前因输尿管癌接受了左肾输尿管切除术。上消化道内镜检查显示十二指肠黏膜水肿、狭窄和点状发红,并进行了活检。组织学分析显示大量 Mott 细胞浸润固有膜黏膜,诊断为 RBD。腹部计算机断层扫描发现与十二指肠相邻的腹膜后有肿块病变,经活检诊断为转移性尿路上皮癌。肿瘤细胞产生的趋化因子可能导致了本例 RBD。

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本文引用的文献

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Isolated Russell body duodenitis.
Dig Dis Sci. 2011 Jul;56(7):2202-4. doi: 10.1007/s10620-010-1559-9. Epub 2011 Jan 14.
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