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罗萨达-多夫曼病:乳腺受累-病例报告及文献复习。

Rosai-Dorfman Disease: Breast Involvement-Case Report and Literature Review.

机构信息

Department of Obstetrics and Gynecology, Filantropia Clinical Hospital of Obstetrics and Gynecology, 11-13 Ion Mihalache Bvd, 011171 Bucharest, Romania.

Department of General Surgery, Emergency University Hospital, 169 Independentei Street, 050098 Bucharest, Romania.

出版信息

Medicina (Kaunas). 2021 Oct 27;57(11):1167. doi: 10.3390/medicina57111167.

Abstract

: Rosai-Dorfman disease (RDD) is a type of histiocytosis that usually appears in young adults or children as bilateral cervical lymphadenopathy, but extranodal involvement in not uncommon. Although the pathogenesis is not entirely elucidated, recent studies showed a possible neoplastic process. : Our manuscript presents a rare case of Rosai-Dorfman disease of the breast, the management of this rare case, and a literature review. There are few cases reported of RDD of the breast (around 90 globally reported cases); the data is poor, and the management not yet standardized for these cases. The case reported here shows the importance of correct breast investigation, breast imaging, and ultrasound-guided biopsy that provided an accurate diagnosis and guided further management. : Although RDD of the breast was rarely presented as bilateral disease in other case reports, our case showed bilateral breast disease with the suspicion of breast cancer on imaging. Pathology and immunohistochemistry were of critical importance and showed a specific pattern for histiocytosis. A multidisciplinary approach was taken into consideration for these cases in order to establish the approach. Some patients underwent surgery, but watchful waiting and close follow-up were the preferred approach. : RDD of the breast is a rare form of histiocytosis, with fewer than 100 globally published cases. Although the management of this disease is not established yet by guidelines, a follow-up approach should be enough for these patients, and surgery might be overtreatment. Mortality from RDD is very low due to comorbidities. A multidisciplinary team decision is important, and abstinence might significantly benefit these patients.

摘要

罗萨达-多夫曼病(RDD)是一种组织细胞增生症,通常在年轻人或儿童中表现为双侧颈部淋巴结病,但也常见结外受累。虽然发病机制尚未完全阐明,但最近的研究表明可能存在肿瘤过程。

我们的手稿介绍了一例罕见的乳腺罗萨达-多夫曼病,这些罕见病例的治疗方法以及文献复习。全球报告的 RDD 乳腺病例(约 90 例)较少;数据不足,这些病例的管理尚未标准化。本报告中的病例表明正确的乳腺检查、乳腺成像和超声引导活检的重要性,这些检查提供了准确的诊断并指导了进一步的管理。

虽然其他病例报告中罕见的 RDD 乳腺表现为双侧疾病,但我们的病例表现为双侧乳腺疾病,影像学上怀疑为乳腺癌。病理学和免疫组织化学具有重要意义,显示出组织细胞增生的特定模式。为了确定治疗方法,考虑采用多学科方法治疗这些病例。一些患者接受了手术,但观察等待和密切随访是首选方法。

乳腺 RDD 是一种罕见的组织细胞增生症,全球发表的病例少于 100 例。虽然该疾病的管理尚未由指南确立,但对于这些患者,随访方法应该足够,手术可能是过度治疗。由于合并症,RDD 的死亡率非常低。多学科团队的决策很重要,节制可能会使这些患者显著受益。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4493/8624438/835d8611fd92/medicina-57-01167-g001.jpg

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