不寻常的大块硬化性血管瘤样结节变

iRadiology Pub Date : 2024-10-26 DOI:10.1002/ird3.103
Maoli Xu, Zhibing Ruan
{"title":"不寻常的大块硬化性血管瘤样结节变","authors":"Maoli Xu,&nbsp;Zhibing Ruan","doi":"10.1002/ird3.103","DOIUrl":null,"url":null,"abstract":"<p>A 23-year-old man was admitted to the hospital after a physical examination revealed a space-occupying lesion in the spleen that had been present for over 2 months. The patient reported no significant symptoms, and laboratory tests showed no abnormalities. Abdominal computed tomography (CT) and abdominal magnetic resonance imaging scans identified a large soft tissue mass in the spleen, measuring 7.1 cm × 5.4 cm × 6.6 cm. A laparoscopic splenectomy was performed. During the procedure, the mass was observed to be dark red, encapsulated, and of medium consistency. Histological examination revealed destruction of the spleen's red and white pulp structure, with notable infiltration of lymphocytes, plasma cells, and histiocytes. Additionally, fibrous tissue hyperplasia and hyalinosis were present, with lobulated nodules forming in certain areas. Immunohistochemical staining results were positive for Vim, CD31, CD4, CD8, CD20, CD3, CD68, SMA, and IgG. The final pathological diagnosis was sclerosing hemangiomatoid nodular transformation of the spleen (sinus lacunar type; Figure 1).</p><p><b>Maoli Xu</b>: Writing—original draft (equal). <b>Zhibing Ruan</b>: Supervision (equal).</p><p>The authors declare that they have no conflicts of interest.</p><p>Not applicable.</p><p>The patient provided written informed consent at the time of entering this study.</p>","PeriodicalId":73508,"journal":{"name":"iRadiology","volume":"2 5","pages":"522-523"},"PeriodicalIF":0.0000,"publicationDate":"2024-10-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/ird3.103","citationCount":"0","resultStr":"{\"title\":\"An unusual large mass of sclerosing angiomatoid nodular transformation\",\"authors\":\"Maoli Xu,&nbsp;Zhibing Ruan\",\"doi\":\"10.1002/ird3.103\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>A 23-year-old man was admitted to the hospital after a physical examination revealed a space-occupying lesion in the spleen that had been present for over 2 months. The patient reported no significant symptoms, and laboratory tests showed no abnormalities. Abdominal computed tomography (CT) and abdominal magnetic resonance imaging scans identified a large soft tissue mass in the spleen, measuring 7.1 cm × 5.4 cm × 6.6 cm. A laparoscopic splenectomy was performed. During the procedure, the mass was observed to be dark red, encapsulated, and of medium consistency. Histological examination revealed destruction of the spleen's red and white pulp structure, with notable infiltration of lymphocytes, plasma cells, and histiocytes. Additionally, fibrous tissue hyperplasia and hyalinosis were present, with lobulated nodules forming in certain areas. Immunohistochemical staining results were positive for Vim, CD31, CD4, CD8, CD20, CD3, CD68, SMA, and IgG. The final pathological diagnosis was sclerosing hemangiomatoid nodular transformation of the spleen (sinus lacunar type; Figure 1).</p><p><b>Maoli Xu</b>: Writing—original draft (equal). <b>Zhibing Ruan</b>: Supervision (equal).</p><p>The authors declare that they have no conflicts of interest.</p><p>Not applicable.</p><p>The patient provided written informed consent at the time of entering this study.</p>\",\"PeriodicalId\":73508,\"journal\":{\"name\":\"iRadiology\",\"volume\":\"2 5\",\"pages\":\"522-523\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-10-26\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://onlinelibrary.wiley.com/doi/epdf/10.1002/ird3.103\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"iRadiology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/ird3.103\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"iRadiology","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/ird3.103","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

一名 23 岁的男子因体检发现脾脏出现占位性病变两个多月而入院。患者无明显症状,实验室检查也未发现异常。腹部计算机断层扫描(CT)和腹部磁共振成像扫描发现脾脏内有一个巨大的软组织肿块,大小为 7.1 厘米 × 5.4 厘米 × 6.6 厘米。患者接受了腹腔镜脾脏切除术。在手术过程中,观察到肿块呈暗红色、包裹状,稠度适中。组织学检查显示,脾脏的红髓和白髓结构遭到破坏,淋巴细胞、浆细胞和组织细胞明显浸润。此外,还出现纤维组织增生和透明变性,某些区域形成分叶状结节。免疫组化染色结果显示,Vim、CD31、CD4、CD8、CD20、CD3、CD68、SMA 和 IgG 均呈阳性。最终病理诊断为脾脏硬化性血管瘤样结节变(窦腔型;图 1):徐茂莉:写作-原稿(等同)。阮志兵:指导(等同):作者声明无利益冲突。不适用。患者在参与本研究时提供了书面知情同意书。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

An unusual large mass of sclerosing angiomatoid nodular transformation

An unusual large mass of sclerosing angiomatoid nodular transformation

A 23-year-old man was admitted to the hospital after a physical examination revealed a space-occupying lesion in the spleen that had been present for over 2 months. The patient reported no significant symptoms, and laboratory tests showed no abnormalities. Abdominal computed tomography (CT) and abdominal magnetic resonance imaging scans identified a large soft tissue mass in the spleen, measuring 7.1 cm × 5.4 cm × 6.6 cm. A laparoscopic splenectomy was performed. During the procedure, the mass was observed to be dark red, encapsulated, and of medium consistency. Histological examination revealed destruction of the spleen's red and white pulp structure, with notable infiltration of lymphocytes, plasma cells, and histiocytes. Additionally, fibrous tissue hyperplasia and hyalinosis were present, with lobulated nodules forming in certain areas. Immunohistochemical staining results were positive for Vim, CD31, CD4, CD8, CD20, CD3, CD68, SMA, and IgG. The final pathological diagnosis was sclerosing hemangiomatoid nodular transformation of the spleen (sinus lacunar type; Figure 1).

Maoli Xu: Writing—original draft (equal). Zhibing Ruan: Supervision (equal).

The authors declare that they have no conflicts of interest.

Not applicable.

The patient provided written informed consent at the time of entering this study.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
×
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