Rosai-Dorfman病伴发阑尾和直肠肿块并伴有igg4阳性浆细胞的独特表现

IF 0.6 Q4 ONCOLOGY Case Reports in Oncological Medicine Pub Date : 2020-10-09 eCollection Date: 2020-01-01 DOI:10.1155/2020/8814871
Jenna J Poldemann, Benjamin H Hinrichs, Abouelmagd Makramalla
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摘要

rossai - dorfman病(RDD),或窦性组织细胞增多症伴大量淋巴结病,是一种罕见的非朗格汉斯细胞性组织细胞增多症。我们报告一例69岁男性阑尾和直肠并发肿块的病例,他接受了ct引导下的经皮活检。组织病理学诊断为RDD伴igg4阳性浆细胞。它被认为是RDD的一个子集,与igg4相关疾病具有相似的特征,表明这两种疾病存在一些重叠。由于胃肠道RDD占结外疾病的不到1%,因此认识到这一实体以指导治疗非常重要。我们回顾胃肠道RDD的表现、诊断和治疗,并讨论可能与igg4相关疾病的重叠。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Unique Presentation of Rosai-Dorfman Disease as Concomitant Appendiceal and Rectal Masses with IgG4-Positive Plasma Cells Diagnosed by Core Needle Biopsy.

Rosai-Dorfman disease (RDD), or sinus histiocytosis with massive lymphadenopathy, is a rare non-Langerhans cell histiocytosis. We report a case of a 69-year-old male with concurrent appendiceal and rectal masses who underwent CT-guided percutaneous biopsy. Histopathology confirmed a diagnosis of RDD with IgG4-positive plasma cells. It is believed to be a subset of RDD that shares similar features with IgG4-related disease suggesting some overlap of the two diseases. Because gastrointestinal RDD accounts for less than 1% of extranodal disease, it is important to recognize this entity in order to guide management. We review the presentation, diagnosis, and treatment of gastrointestinal RDD and discuss the possible overlap with IgG4-related disease.

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来源期刊
自引率
0.00%
发文量
11
审稿时长
16 weeks
期刊介绍: Case Reports in Oncological Medicine is a peer-reviewed, Open Access journal that publishes case reports and case series related to breast cancer, lung cancer, gastrointestinal cancer, skin cancer, head and neck cancer, paediatric oncology, neurooncology as well as genitourinary cancer.
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