Granular cell tumor of the lung and tracheobronchial tree: Two case-presentation with a review of the literature.

IF 0.9 Q4 ONCOLOGY Rare Tumors Pub Date : 2023-01-01 DOI:10.1177/20363613231187822
Yoldez Houcine, Mouna Mlika, Chirine Moussa, Houda Rouis, Emna Brahem, Olfa Ismail, Sonia Maȃlej, Faouzi El Mezni
{"title":"Granular cell tumor of the lung and tracheobronchial tree: Two case-presentation with a review of the literature.","authors":"Yoldez Houcine,&nbsp;Mouna Mlika,&nbsp;Chirine Moussa,&nbsp;Houda Rouis,&nbsp;Emna Brahem,&nbsp;Olfa Ismail,&nbsp;Sonia Maȃlej,&nbsp;Faouzi El Mezni","doi":"10.1177/20363613231187822","DOIUrl":null,"url":null,"abstract":"<p><p>Pulmonary granular cells tumors (CGT) are rare tumors, that derive from Schwann cells. In the tracheobronchial and pulmonary tree, they remain a diagnostic challenge. There are no well-established criteria to differentiate between benign, atypical, and malignant GCT. Moreover, its real frequency in the respiratory tract is still unknown. Here, we represent 2 cases of bronchial and lung GCTs. We aim to highlight the frequency of all clinicopathological characteristics of this rare tumor in the tracheobronchial and pulmonary tree location based on our cases and the available literature in a large systematic review.</p>","PeriodicalId":46078,"journal":{"name":"Rare Tumors","volume":null,"pages":null},"PeriodicalIF":0.9000,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/4c/ef/10.1177_20363613231187822.PMC10338731.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Rare Tumors","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1177/20363613231187822","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"ONCOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Pulmonary granular cells tumors (CGT) are rare tumors, that derive from Schwann cells. In the tracheobronchial and pulmonary tree, they remain a diagnostic challenge. There are no well-established criteria to differentiate between benign, atypical, and malignant GCT. Moreover, its real frequency in the respiratory tract is still unknown. Here, we represent 2 cases of bronchial and lung GCTs. We aim to highlight the frequency of all clinicopathological characteristics of this rare tumor in the tracheobronchial and pulmonary tree location based on our cases and the available literature in a large systematic review.

Abstract Image

Abstract Image

Abstract Image

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
肺及气管支气管树状颗粒细胞瘤:两例报告并文献复习。
肺颗粒细胞瘤(CGT)是一种罕见的肿瘤,起源于雪旺细胞。在气管支气管和肺部,它们仍然是一个诊断挑战。没有明确的标准来区分良性、非典型和恶性GCT。此外,其在呼吸道的真实频率尚不清楚。在这里,我们报告了2例支气管和肺部的gct。我们的目的是根据我们的病例和现有的文献,在一个大型的系统回顾中强调所有临床病理特征在气管支气管和肺树位置的罕见肿瘤的频率。
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
Rare Tumors
Rare Tumors ONCOLOGY-
CiteScore
1.50
自引率
0.00%
发文量
15
审稿时长
15 weeks
期刊最新文献
The efficacy of combination immunotherapy with ipilimumab plus nivolumab in metastatic myxofibrosarcoma. Surgical management of a chest wall osteosarcoma with pleural and lung invasion through en-bloc chest resection and complex reconstruction. Case report. Exploration of the causative gene in a case of multiple nevoid basal cell carcinoma: A case report. Comprehensive study of ancient schwannoma: Exploring histomorphological diversity and diagnostic challenges. Novel MEN1-associated retroperitoneal pleomorphic liposarcoma.
×
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