Immunohistochemical Analysis of Endothelial Cells in Vascular Transformation of Lymph Node Sinuses: Vascular or Lymphatic Differentiation?

作者
Basma Basha,Eric D. Hsi
出处
期刊:Applied Immunohistochemistry & Molecular Morphology [Lippincott Williams & Wilkins]
卷期号:27 (6): 482-489 被引量:12
标识
DOI:10.1097/pai.0000000000000661
摘要

INTRODUCTION: Vascular transformation of sinuses (VTS) is an uncommon and benign lesion, defined by conversion of lymph node sinuses into complex, anatomizing and endothelial-lined channels. Despite the name of VTS, which implies a change in differentiation from lymphatic to vascular endothelium, very few studies have systematically examined VTS with modern immunohistochemical markers commonly used in clinical laboratories. It is unclear whether endothelial cells in VTS display pure vascular or lymphatic differentiation, or both. DESIGN: A total of 11 cases with a diagnosis of VTS (identified in the tissue archives of the Cleveland Clinic between 1992 and 2015) were reviewed and confirmed. Twenty cases of benign lymph nodes without specific diagnoses were used as control tissues. Immunohistochemical stains were performed on formalin-fixed, paraffin-embedded lymph node tissue using an automated immunohistochemistry platform with antibodies against CD31, CD34, D2-40, and ERG. Positivity in the VTS lesions was defined as distinct expression in the appropriate cell compartment in ≥20% of cells. In control cases, staining was evaluated in both vascular and lymphatic channels-vascular structures were identified by presence of red cells or well-formed vascular walls and lymphatics by anatomic location and absence of vascular features. RESULTS: In the VTS lesions, D2-40 expression was absent in the lesional endothelial cells of 5/11 (45%) cases. In the cases lacking D240 expression, uninvolved lymphatic endothelium maintained expression. CD34 expression was also seen in 6/11 (54%), CD31 was seen in 10/11 (90%), and ERG expression was seen in all cases. In all the control cases, D240 expression was exclusively seen in lymphatic endothelial cells and not seen in vascular endothelial cells (eg, vascular channels in the hilum). CD34 was weakly positive in the lymphatic endothelium of only 7/20 (35%) control cases, but expressed in 20/20 (100%) control cases in the vascular endothelium. 20/20 (100%) of control cases showed expression of CD31 and ERG in both vascular and lymphatic endothelium. CONCLUSION: VTS lesional endothelial cells demonstrate patterns of vascular markers that show mixed blood vascular and lymphatic features. There appears to be a degree of alignment toward endothelial differentiation with decreased expression of D2-40 in some cases.

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
1秒前
2秒前
2秒前
桐桐应助掏粪男孩采纳,获得10
3秒前
QwQ完成签到,获得积分10
3秒前
陈老师耶发布了新的文献求助10
3秒前
不爱吃西瓜关注了科研通微信公众号
4秒前
6秒前
杨乃彬完成签到,获得积分10
7秒前
shirleen完成签到,获得积分10
7秒前
852应助禹宛白采纳,获得10
8秒前
无花果应助feifei采纳,获得30
8秒前
张欢馨应助feifei采纳,获得10
8秒前
叮叮当当当完成签到 ,获得积分10
9秒前
9秒前
橘皮乌龙完成签到,获得积分10
10秒前
陶陶发布了新的文献求助10
11秒前
r93527005完成签到,获得积分10
11秒前
13秒前
慕青应助李Xinyao_29采纳,获得10
13秒前
13秒前
14秒前
14秒前
张欢馨应助保守的迫击炮采纳,获得10
14秒前
15秒前
Akim应助无敌小行星采纳,获得30
15秒前
QwQ发布了新的文献求助10
15秒前
15秒前
烟花应助掏粪男孩采纳,获得10
16秒前
17秒前
17秒前
17秒前
言瓒发布了新的文献求助30
17秒前
Danmer发布了新的文献求助10
17秒前
搜集达人应助科研通管家采纳,获得10
17秒前
17秒前
cdercder应助科研通管家采纳,获得10
17秒前
17秒前
Lucas应助科研通管家采纳,获得10
18秒前
852应助科研通管家采纳,获得10
18秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Römisch-Germanische Forschungen 1000
China Pluperfect I: Epistemology of Past and Outside in Chinese Art 520
Matrix Methods in Data Mining and Pattern Recognition Second Edition 510
The fast track to determining transfer functions of linear circuits: The student guide 500
The Analytical and Numerical Solution of Electric and Magnetic Fields 500
Green Fire Retardants for Polymeric Materials 400
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 内科学 物理 复合材料 催化作用 细胞生物学 无机化学 光电子学 物理化学 电极 基因
热门帖子
关注 科研通微信公众号,转发送积分 7617029
求助须知:如何正确求助?哪些是违规求助? 9192384
关于积分的说明 19699911
捐赠科研通 7189502
什么是DOI,文献DOI怎么找? 3271994
关于科研通互助平台的介绍 2434749
邀请新用户注册赠送积分活动 2266986