Comprehensive Investigation of Angiogenesis, PASS Score and Immunohistochemical Factors in Risk Assessment of Malignancy for Paraganglioma and Pheochromocytoma

Author:

Milinkovic Marija1,Soldatovic Ivan2,Zivaljevic Vladan3,Bozic Vesna1,Zivotic Maja4ORCID,Tatic Svetislav4,Dundjerovic Dusko4ORCID

Affiliation:

1. Department of Pathology, University Clinical Center of Serbia, 11000 Belgrade, Serbia

2. Institute for Medical Statistics and Informatics, Faculty of Medicine, University of Belgrade, 11000 Belgrade, Serbia

3. Clinic for Endocrine Surgery, University Clinical Center of Serbia, 11000 Belgrade, Serbia

4. Institute of Pathology, Faculty of Medicine, University of Belgrade, 11000 Belgrade, Serbia

Abstract

A challenging task in routine practice is finding the distinction between benign and malignant paragangliomas and pheochromocytomas. The aim of this study is to conduct a comparative analysis of angiogenesis by assessing intratumoral microvascular density (MVD) with immunohistochemical (IHC) markers (CD31, CD34, CD105, ERG), and S100 immunoreactivity, Ki67 proliferative index, succinate dehydrogenase B (SDHB) expressiveness, tumor size with one the most utilized score Pheochromocytoma of Adrenal Gland Scales Score (PASS), using tissue microarray (TMA) with 115 tumor samples, 61 benign (PASS < 4) and 54 potentially malignant (PASS ≥ 4). We found no notable difference between intratumoral MVD and potentially malignant behavior. The group of potentially malignant tumors is significantly larger in size, has lower intratumoral MVD, and a decreased number of S100 labeled sustentacular cells. Both groups have low proliferative activity (mean Ki67 is 1.02 and 1.22, respectively). Most tumors maintain SDHB expression, only 6 cases (5.2%) showed a loss of expression (4 of them in PASS < 4 group and 2 in PASS ≥ 4). PASS score is easily available for assessment and complemented with markers of biological behavior to complete the risk stratification algorithm. Size is directly related to PASS score and malignancy. Intratumoral MVD is extensively developed but it is not crucial in evaluating the malignant potential.

Funder

Ministry of Education and Science of the Republic of Serbia

Publisher

MDPI AG

Reference62 articles.

1. Overview of the 2022 WHO Classification of Paragangliomas and Pheochromocytomas;Mete;Endocr. Pathol.,2022

2. Update on Adrenal Tumors in 2017 World Health Organisation (WHO) of Endocrine Tumours;Lam;Endocr. Pathol.,2017

3. Lloyd, R.V., Osamura, R.Y., Kloppel, G., and Rosai, J. (2017). WHO Classification of Tumours of Endocrine Organs: Pathology and Genetics of Tumours of Endocrine Organ, IARC Press. [4th ed.].

4. Inherited mutations in pheochromocytoma and paraganglioma: Why all patients should be offered genetic testing;Fishbein;Ann. Surg. Oncol.,2013

5. Pheochromocytoma and paraganglioma pathogenesis: Learning from genetic heterogeneity;Dahia;Nat. Rev. Cancer,2014

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3