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Recurrent glomangioma("true"glomus tumor)of the middle ear and mastoid 被引量:1
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作者 Adam C.Kaufman Jason A.Brant +2 位作者 Neil N.Luu Virginia A.LiVolsi Douglas C.Bigelow 《World Journal of Otorhinolaryngology-Head and Neck Surgery》 2019年第4期175-179,共5页
Objective:To review current literature and experience with glomangiomas,or true glomus tumors of the middle ear and mastoid as well asto report on the exceptionally rare case of a glomangiomastemming from the middle e... Objective:To review current literature and experience with glomangiomas,or true glomus tumors of the middle ear and mastoid as well asto report on the exceptionally rare case of a glomangiomastemming from the middle ear space with multiple recurrences.Methods:Review of existing world literature and description of personal experience with rare cases of a glomangioma of the middle ear and mastoid.Results:Review of existing literature revealed two cases of patients presenting with tinnitus and hearing loss refractory to medical management.Both patients were ultimately diagnosed with glomangioma on histopathology.Complete surgical excision is thought to be curative.Patient:A 36-year-old woman presented with a rare case of a glomangioma of the middle ear presenting with unilateral hearing loss.She was noted to have a mass behind the tympanic membrane.Imaging revealed a diffuse mass filling the mastoid air cells.Imaging characteristics and histology were consistent with a glomangioma.Intervention:Initial resection via mastoidectomy using a postauricular approach.The tympanic membrane was reconstructed with temporalis tissue.Follow-up revision tympanomas-toidectomy was performed upon recurrence of disease.The chorda tympani were sacrificed due to tumor involvement.The incus and head of the malleus were removed to gain better access to the tumor.The ossicular chain was reconstructed with a Goldenberg Total Ossicular Prosthesis.Main outcome measure:Recurrence of disease.Follow-up:In the 67 months since her most recent surgery,there has been no evidence of recurrence by CT or physical exam.Conclusion:Glomangioma of the middle ear represents an exceptionally rare entity that can present in a similar fashion to a paraganglioma. 展开更多
关键词 glomangioma Glomus tumor Glomuvenous malformation Middle ear tumor Unilateral hearing loss
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甲外多发性球血管瘤1例报道并文献复习 被引量:1
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作者 孔秀珍 张玲 +1 位作者 杨庆玲 步新娟 《罕少疾病杂志》 2007年第4期27-30,共4页
目的探讨球血管瘤的临床病理特点及诊断和鉴别诊断,以减少误诊。方法用回顾性方法分析1例发生于甲外部位的多发性球血管瘤并进行文献复习。结果多发性球血管瘤很少见,其临床症状与经典型血管球瘤相似,以疼痛为主。病理组织学上表现为其... 目的探讨球血管瘤的临床病理特点及诊断和鉴别诊断,以减少误诊。方法用回顾性方法分析1例发生于甲外部位的多发性球血管瘤并进行文献复习。结果多发性球血管瘤很少见,其临床症状与经典型血管球瘤相似,以疼痛为主。病理组织学上表现为其血管成分为较大的静脉,似海绵状血管瘤,瘤细胞沿血管内壁成层状排列或成簇聚集。治疗方法为手术切除。结论多发性球血管瘤是血管球瘤的一种少见类型,病理学上应与海绵状血管瘤和动静脉血管瘤等鉴别。 展开更多
关键词 球血管瘤 血管球瘤 血管瘤 指甲
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血管球瘤的光镜和电镜观察
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作者 王弘 刘文杰 《石河子大学学报(自然科学版)》 CAS 1992年第3期35-38,共4页
本文报道了7例血管球瘤的光镜和电镜观察结果。光镜下肿瘤组织由毛细血管网和围绕这些血管的肿瘤细胞群组成。电镜下肿瘤细胞主要具有平滑肌细胞的超微结构特征,毛细血管结构正常。
关键词 血管球瘤 光学显微镜 电子显微镜 超微结构
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右上肢单发球血管瘤1例
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作者 陈佳雯 陈文 +2 位作者 肖芷珣 彭佳美 纪超 《中国皮肤性病学杂志》 CAS CSCD 北大核心 2022年第7期836-838,共3页
患者男,50岁,右上肢蓝紫色丘疹10年。皮肤科情况:右上肢可见孤立蓝紫色丘疹,表面可见毛细血管扩张,周围可见红晕,压痛明显。手术切除后组织病理学为典型球血管瘤表现。甲外球血管瘤少见,本病例可为今后甲外球血管瘤的正确诊断提供帮助。
关键词 球血管瘤 甲外球血管瘤
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