Castleman disease as the great mimicker: the role of complex morpho-pathological evaluation.

IF 1.2 4区 医学 Q4 DEVELOPMENTAL BIOLOGY
Ionuţ Tănase, Caius Codruţ Sarafoleanu, Bogdan Mihail Cobzeanu, Alina Maria Georgescu, Constantin Ioan Busuioc, Dan Iovănescu, Florentina Carmen Badea
{"title":"Castleman disease as the great mimicker: the role of complex morpho-pathological evaluation.","authors":"Ionuţ Tănase, Caius Codruţ Sarafoleanu, Bogdan Mihail Cobzeanu, Alina Maria Georgescu, Constantin Ioan Busuioc, Dan Iovănescu, Florentina Carmen Badea","doi":"10.47162/RJME.65.4.03","DOIUrl":null,"url":null,"abstract":"<p><p>Castleman disease (CD) is a group of lymphoproliferative disorders characterized by abnormal enlargement of lymph nodes (LNs) and a wide range of symptoms. Only a few cases are found in the head and neck. Based on clinical presentation and evolution, the disease can be classified into two main subtypes: unicentric CD (UCD), characterized by the enlargement of a single LN or a single LN chain, and multicentric CD (MCD), characterized by the involvement of multiple LNs and regions, with more important systemic symptoms and a poor prognosis. CD is also known as \"the great mimicker\" and can be easily misdiagnosed, sharing similar clinical and imaging characteristics with other pathologies, mainly when it is found in the neck. A histopathological (HP) and immunohistochemical (IHC) correlation is essential in these cases to accurately diagnose and establish the proper treatment plan. In light of this, we present a rare case of a 15-year-old young female with a slowly expanding, isolated supraclavicular mass. An excisional biopsy was performed, and the results confirmed the presence of CD, hyaline-vascular type. As of this writing, there was no evidence of recurrence or new enlarged LNs. We also review CD's clinical and HP features and the diagnostic and treatment challenges it poses.</p>","PeriodicalId":54447,"journal":{"name":"Romanian Journal of Morphology and Embryology","volume":"65 4","pages":"575-581"},"PeriodicalIF":1.2000,"publicationDate":"2024-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Romanian Journal of Morphology and Embryology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.47162/RJME.65.4.03","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"DEVELOPMENTAL BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Castleman disease (CD) is a group of lymphoproliferative disorders characterized by abnormal enlargement of lymph nodes (LNs) and a wide range of symptoms. Only a few cases are found in the head and neck. Based on clinical presentation and evolution, the disease can be classified into two main subtypes: unicentric CD (UCD), characterized by the enlargement of a single LN or a single LN chain, and multicentric CD (MCD), characterized by the involvement of multiple LNs and regions, with more important systemic symptoms and a poor prognosis. CD is also known as "the great mimicker" and can be easily misdiagnosed, sharing similar clinical and imaging characteristics with other pathologies, mainly when it is found in the neck. A histopathological (HP) and immunohistochemical (IHC) correlation is essential in these cases to accurately diagnose and establish the proper treatment plan. In light of this, we present a rare case of a 15-year-old young female with a slowly expanding, isolated supraclavicular mass. An excisional biopsy was performed, and the results confirmed the presence of CD, hyaline-vascular type. As of this writing, there was no evidence of recurrence or new enlarged LNs. We also review CD's clinical and HP features and the diagnostic and treatment challenges it poses.

卡斯特曼病(CD)是一组淋巴细胞增生性疾病,以淋巴结异常肿大和多种症状为特征。只有少数病例发生在头颈部。根据临床表现和演变,该病可分为两大亚型:单中心 CD(UCD)和多中心 CD(MCD),前者以单个淋巴结或单个淋巴结链肿大为特征,后者以多个淋巴结和淋巴结区域受累为特征,伴有更重要的全身症状,预后较差。CD 也被称为 "伟大的模仿者",很容易被误诊,因为它与其他病变具有相似的临床和影像学特征,主要是在颈部发现时。在这些病例中,组织病理学(HP)和免疫组织化学(IHC)的相关性对于准确诊断和制定适当的治疗方案至关重要。有鉴于此,我们报告了一例罕见病例,患者是一名 15 岁的年轻女性,其锁骨上肿块缓慢扩大且孤立存在。我们对该病例进行了切除活检,结果证实其为透明-血管型 CD。截至本文撰写之时,没有证据表明该病复发或出现新的肿大 LN。我们还回顾了 CD 的临床和 HP 特征,以及它给诊断和治疗带来的挑战。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
1.70
自引率
20.00%
发文量
221
审稿时长
3-8 weeks
期刊介绍: Romanian Journal of Morphology and Embryology (Rom J Morphol Embryol) publishes studies on all aspects of normal morphology and human comparative and experimental pathology. The Journal accepts only researches that utilize modern investigation methods (studies of anatomy, pathology, cytopathology, immunohistochemistry, histochemistry, immunology, morphometry, molecular and cellular biology, electronic microscopy, etc.).
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信