上颌窦副神经节瘤合并Addison病(血管性肿瘤)1例

Sami A Alkindy
{"title":"上颌窦副神经节瘤合并Addison病(血管性肿瘤)1例","authors":"Sami A Alkindy","doi":"10.5430/JST.V7N1P7","DOIUrl":null,"url":null,"abstract":"Paraganglioma of the nasal and paranasal sinuses are quite rare neuroendocrine tumours, usually hormonally inactive, presentingas nasal polyps with or without epistaxis. We present a rare case of a 23 year old male, with Addison’s disease, who was referredfrom endocrinology department with a complaint of right nasal blockage associated with recurrent epistaxis. A provisionalclinical diagnosis of vascular tumour was made, Computed tomography and MRI suggested hemangioma /inverted papilloma.However, biopsy reported a highly vascular tissue mimicking angiofibroma, further immunostaining studies with Synaptophysinand S-100 confirmed the diagnosis of Paraganglioma. This rare tumour in the paranasal sinuses may mimic vascular tumour andcan only be confirmed with histopathological immunostains studies. According to our knowledge, this is first case reported to beassociated with Addison’s disease in the English literature.","PeriodicalId":17174,"journal":{"name":"Journal of Solid Tumors","volume":"209 1","pages":"7"},"PeriodicalIF":0.0000,"publicationDate":"2016-09-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"Paraganglioma of maxillary sinus associated with Addison’s disease mimicking a vascular tumour: A case report\",\"authors\":\"Sami A Alkindy\",\"doi\":\"10.5430/JST.V7N1P7\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Paraganglioma of the nasal and paranasal sinuses are quite rare neuroendocrine tumours, usually hormonally inactive, presentingas nasal polyps with or without epistaxis. We present a rare case of a 23 year old male, with Addison’s disease, who was referredfrom endocrinology department with a complaint of right nasal blockage associated with recurrent epistaxis. A provisionalclinical diagnosis of vascular tumour was made, Computed tomography and MRI suggested hemangioma /inverted papilloma.However, biopsy reported a highly vascular tissue mimicking angiofibroma, further immunostaining studies with Synaptophysinand S-100 confirmed the diagnosis of Paraganglioma. This rare tumour in the paranasal sinuses may mimic vascular tumour andcan only be confirmed with histopathological immunostains studies. According to our knowledge, this is first case reported to beassociated with Addison’s disease in the English literature.\",\"PeriodicalId\":17174,\"journal\":{\"name\":\"Journal of Solid Tumors\",\"volume\":\"209 1\",\"pages\":\"7\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2016-09-13\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Solid Tumors\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.5430/JST.V7N1P7\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Solid Tumors","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.5430/JST.V7N1P7","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1

摘要

鼻窦和副鼻窦神经节瘤是一种罕见的神经内分泌肿瘤,通常为激素活性低下,表现为鼻息肉,伴或不伴鼻出血。我们报告一例罕见的23岁男性艾迪生病患者,从内分泌科转诊,主诉右鼻阻塞伴复发性鼻出血。初步临床诊断为血管瘤,ct及MRI提示为血管瘤/内翻性乳头状瘤。然而,活检报告了高度血管性组织模拟血管纤维瘤,进一步用synaptophysin和S-100免疫染色研究证实了副神经节瘤的诊断。这种罕见的肿瘤发生在鼻窦,可能与血管肿瘤相似,只能通过组织病理学免疫染色研究来证实。据我们所知,这是英国文献中第一例与艾迪生病相关的病例。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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
Paraganglioma of maxillary sinus associated with Addison’s disease mimicking a vascular tumour: A case report
Paraganglioma of the nasal and paranasal sinuses are quite rare neuroendocrine tumours, usually hormonally inactive, presentingas nasal polyps with or without epistaxis. We present a rare case of a 23 year old male, with Addison’s disease, who was referredfrom endocrinology department with a complaint of right nasal blockage associated with recurrent epistaxis. A provisionalclinical diagnosis of vascular tumour was made, Computed tomography and MRI suggested hemangioma /inverted papilloma.However, biopsy reported a highly vascular tissue mimicking angiofibroma, further immunostaining studies with Synaptophysinand S-100 confirmed the diagnosis of Paraganglioma. This rare tumour in the paranasal sinuses may mimic vascular tumour andcan only be confirmed with histopathological immunostains studies. According to our knowledge, this is first case reported to beassociated with Addison’s disease in the English literature.
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
期刊最新文献
Description of multiparametric targeting techniques for stereotactic arrhythmia radioablation in refractory ventricular tachycardia: A quaternary medical center experience Prognostic significance of pretreatment inflammatory biomarkers in non-metastatic breast cancer Prognostic significance of SOX2 and GPC3 in Ameloblastoma and its malignant counterpart (Ameloblastic Carcinoma) Tumor stroma ratio as a parameter for prognosis and clinicopathological behavior of oral squamous cell carcinoma: A retrospective cohort study A pilot study to evaluate the efficacy of PEC blocks in minimising chronic post-mastectomy pain
×
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