Clinical and immunohistochemical characteristics of pheochromocytomas

A. M. Morozova, O. G. Tsygankova, E. Yurova, N. A. Torokhtiy, K. Stegniy, T. A. Kulakova, R. Goncharuk, M. Dmitriev
{"title":"Clinical and immunohistochemical characteristics of pheochromocytomas","authors":"A. M. Morozova, O. G. Tsygankova, E. Yurova, N. A. Torokhtiy, K. Stegniy, T. A. Kulakova, R. Goncharuk, M. Dmitriev","doi":"10.14341/serg12759","DOIUrl":null,"url":null,"abstract":"BACKGROUND. Currently, pheochromocytomas are classified as malignant tumors (WHO 2017), which means that special postoperative tactics are required for patients with different risks of pheochromocytoma aggressiveness.AIM. Assess the predictors of malignant potential of pheochromocytomas using the GAPP and PASS scales.MATERIALS AND METHODS. From 2016 to 2021, 24 patients diagnosed with pheochromocytoma, age from 18 to 81 years (median 50.4+-3.3), were hospitalized at the Primorsky Regional Center for Diabetes and Endocrine Diseases, 21 of them were women and 3 were men. Hormone producing adenoma in the right adrenal gland was found in 13 patients (54.2%), on the left in 8 (33.3%) cases, bilateral pheochromocytoma — in 3 (12.5%) cases. Clinical manifestation: a sharp increase in systolic blood pressure of more than 200 mmHg accompanied by crises, tachycardia was detected in 14 patients, the rest of the clinical symptoms were nonspecific: persistent arterial hypertension, as well as general weakness. The sizes of the revealed formations varied from — 1.1x1.6x1.6 cm to — 7.7x10.6x8.5 cm. (median 37+-1.2). The diagnosis was confirmed by standard examinations. All patients underwent unilateral adrenalectomy at the Surgery Center of the FEFU Medical Center, using two main methods: retroperitoneoscopy and laparoscopy. After the operation, histological and immunohistochemical studies were performed. The analysis of immunohistochemical studies was carried out. The expression of Ki67, Chromogranin A, Synaptophysin was determined. Since it is currently impossible to absolutely accurately determine the malignant potential of pheochromocytomas, the PASS and GAPP scores have been introduced into clinical practice. A retrospective analysis of the cytological material of patients operated on in 2020 and 2021 was carried out.RESULTS. According to the PASS scale, more than 4 points were detected in 7 out of 10 patients. GAPP scores ranged from 0 to 2 in 3 out of 10 people; 3-6 points for 5; more than 7 points in 2 patients. At the same time, the results of the calculation on both scales in 100% of cases correspond to each other, which makes it possible to identify patients with moderate and high malignant potential.CONCLUSION. The results obtained confirm the need to use additional tools in clinical practice to determine the prognosis in a particular patient, which means it will allow developing an algorithm for dispensary observation, the timing of the follow-up examination.","PeriodicalId":30783,"journal":{"name":"Endokrinnaia khirurgiia","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2022-12-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Endokrinnaia khirurgiia","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.14341/serg12759","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

BACKGROUND. Currently, pheochromocytomas are classified as malignant tumors (WHO 2017), which means that special postoperative tactics are required for patients with different risks of pheochromocytoma aggressiveness.AIM. Assess the predictors of malignant potential of pheochromocytomas using the GAPP and PASS scales.MATERIALS AND METHODS. From 2016 to 2021, 24 patients diagnosed with pheochromocytoma, age from 18 to 81 years (median 50.4+-3.3), were hospitalized at the Primorsky Regional Center for Diabetes and Endocrine Diseases, 21 of them were women and 3 were men. Hormone producing adenoma in the right adrenal gland was found in 13 patients (54.2%), on the left in 8 (33.3%) cases, bilateral pheochromocytoma — in 3 (12.5%) cases. Clinical manifestation: a sharp increase in systolic blood pressure of more than 200 mmHg accompanied by crises, tachycardia was detected in 14 patients, the rest of the clinical symptoms were nonspecific: persistent arterial hypertension, as well as general weakness. The sizes of the revealed formations varied from — 1.1x1.6x1.6 cm to — 7.7x10.6x8.5 cm. (median 37+-1.2). The diagnosis was confirmed by standard examinations. All patients underwent unilateral adrenalectomy at the Surgery Center of the FEFU Medical Center, using two main methods: retroperitoneoscopy and laparoscopy. After the operation, histological and immunohistochemical studies were performed. The analysis of immunohistochemical studies was carried out. The expression of Ki67, Chromogranin A, Synaptophysin was determined. Since it is currently impossible to absolutely accurately determine the malignant potential of pheochromocytomas, the PASS and GAPP scores have been introduced into clinical practice. A retrospective analysis of the cytological material of patients operated on in 2020 and 2021 was carried out.RESULTS. According to the PASS scale, more than 4 points were detected in 7 out of 10 patients. GAPP scores ranged from 0 to 2 in 3 out of 10 people; 3-6 points for 5; more than 7 points in 2 patients. At the same time, the results of the calculation on both scales in 100% of cases correspond to each other, which makes it possible to identify patients with moderate and high malignant potential.CONCLUSION. The results obtained confirm the need to use additional tools in clinical practice to determine the prognosis in a particular patient, which means it will allow developing an algorithm for dispensary observation, the timing of the follow-up examination.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
嗜铬细胞瘤的临床及免疫组织化学特征
背景。目前,嗜铬细胞瘤被归类为恶性肿瘤(世界卫生组织2017),这意味着对于具有不同嗜铬细胞癌侵袭性风险的患者需要特殊的术后策略。目标。使用GAPP和PASS量表评估嗜铬细胞瘤恶性潜能的预测因素。材料和方法。从2016年到2021年,24名被诊断为嗜铬细胞瘤的患者在普里莫尔斯基糖尿病和内分泌疾病区域中心住院,年龄从18岁到81岁(中位数50.4+-3.3),其中21人为女性,3人为男性。13例(54.2%)右侧肾上腺出现激素分泌腺瘤,8例(33.3%)左侧肾上腺出现激素生成腺瘤,3例(12.5%)双侧嗜铬细胞瘤。临床表现:收缩压急剧升高超过200毫米汞柱并伴有危象,14名患者检测到心动过速,其余临床症状为非特异性:持续性动脉高压,以及全身无力。显示的地层大小从-1.1x1.6x1.6厘米到-7.7x10.6x8.5厘米不等(中位数37+/-1.2)。通过标准检查证实了诊断。所有患者在联邦医学院外科中心接受了单侧肾上腺切除术,主要采用两种方法:后腹腔镜和腹腔镜。术后进行组织学和免疫组织化学研究。进行免疫组化研究分析。检测Ki67、嗜铬粒蛋白A、突触素的表达。由于目前无法绝对准确地确定嗜铬细胞瘤的恶性潜能,PASS和GAPP评分已被引入临床实践。对2020年和2021年手术患者的细胞学资料进行了回顾性分析。结果。根据PASS量表,10名患者中有7名检测到4分以上。每10个人中有3个人的GAPP得分在0到2之间;3-6分,5分;超过7分2例。同时,在100%的病例中,两种量表的计算结果相互对应,这使得识别具有中度和高度恶性潜能的患者成为可能。结论。所获得的结果证实了在临床实践中需要使用额外的工具来确定特定患者的预后,这意味着它将允许开发一种用于药房观察和后续检查时间的算法。
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 去求助
来源期刊
自引率
0.00%
发文量
4
审稿时长
6 weeks
期刊最新文献
Insulinoma: analysis of prevalence and incidence in the world In memory of Bondarenko Vladimir Olegovich (07.06.1960–15.08.2022) To the 120th anniversary of the birth of Professor Oleg Vladimirovich Nikolaev (1903–1980) Thyroid functional autonomy — sclerotherapy and radioactive iodine therapy: case report Non-recurrent laryngeal nerve in thyroid and parathyroid surgery
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1