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颈部巨大血管平滑肌瘤1例并文献复习

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文章导航 > 临床耳鼻咽喉头颈外科杂志 > 2019 > 33(3): 280-282
周杰玉, 杨希之, 王振涛. 颈部巨大血管平滑肌瘤1例并文献复习[J]. 临床耳鼻咽喉头颈外科杂志, 2019, 33(3): 280-282. doi: 10.13201/j.issn.1001-1781.2019.03.023
引用本文: 周杰玉, 杨希之, 王振涛. 颈部巨大血管平滑肌瘤1例并文献复习[J]. 临床耳鼻咽喉头颈外科杂志, 2019, 33(3): 280-282. doi: 10.13201/j.issn.1001-1781.2019.03.023
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Giant angioleiomyoma of the neck:a rare tumor case and literature review[J]. J Clin Otorhinolaryngol Head Neck Surg, 2019, 33(3): 280-282. doi: 10.13201/j.issn.1001-1781.2019.03.023
Citation: Giant angioleiomyoma of the neck:a rare tumor case and literature review[J]. J Clin Otorhinolaryngol Head Neck Surg, 2019, 33(3): 280-282. doi: 10.13201/j.issn.1001-1781.2019.03.023
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颈部巨大血管平滑肌瘤1例并文献复习

    • 上海交通大学医学院附属第九人民医院耳鼻咽喉头颈外科 上海市耳鼻疾病转化医学重点实验室 上海交通大学医学院耳科学研究所(上海, 200011)

  • 基金项目:

    上海交通大学医学院附属第九人民医院基础研究助推计划资助 (No:JYZZ005)

详细信息
    通讯作者: 王振涛,E-mail:wangzhentaoo@hotmail.com

  • 中图分类号: R739.91

Giant angioleiomyoma of the neck:a rare tumor case and literature review

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    摘要
  • The patient was admitted of the chief complain "progressive snoring for two years, gradual enlargement of the neck neoplasm for six months".Specific examination indicated that bilateral cervical-mandibular margin to cervical root diffuse apophysis, most notably in the right thyroid plane.Posterior pharyngeal wall underwent an apophysis while no related vein engorgement was noticed.Ultrasound examination indicated that multiple hypoechoic nodules with calcification from posterior thyroid to submandibular.MRI examination indicated bilateral posterior pharyngeal plexus malformation.The patient was first treated with angiography and embolization in the department of interventional and followed by "cervical mass resection" in the department of otorhinolaryngology head and neck surgery.The tumor size was 11 cm×8 cm×3 cm.Histology of the tumor was angioleiomyoma with immunohistochemical results Desmin (+), SMA (+), CD31 (-), CD34 (+), Ki67 (+, 1%), Vimentin (+), D-240 (-), p53 (-).
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    • 参考文献(9)
  • [1]

    WOO K S, KIM S H, KIM H S, et al.Clinical experience with treatment of angioleiomyoma[J].Arch Plast Surg, 2014, 41:374-378.

    [2]

    LIU Y, LI B, LI L, et al.Angioleiomyomas in the head and neck:A retrospective clinical and immunohistochemical analysis[J].Oncol Lett, 2014, 8:241-247.

    [3]

    MATIAKIS A, KARAKOSTAS P, PAVLOU A M, et al.Angioleiomyoma of the oral cavity:a case report and brief review of the literature[J].J Korean Assoc Oral Maxillofac Surg, 2018, 44:136-139.

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    张鑫, 张书玲, 肖士卿.鼻前庭血管平滑肌瘤1例[J].临床耳鼻咽喉头颈外科杂志, 2010, 24 (10):476-476.

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    冯俊, 唐嗣泉, 赵冰琳, 等.喉血管平滑肌瘤1例[J].临床耳鼻咽喉头颈外科杂志, 2007, 21 (10):472-472.

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    SAKAI E, ASAI E, YAMAMOTO T.Acral calcified angioleiomyoma[J].Eur J Dermatol, 2010, 20:121-122.

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    DUBINA M, GOLDENBERG G.Viral-associated nonmelanoma skin cancers:a review[J].Am J Dermatopathol, 2009, 31:561-573.

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    朱国臣, 肖大江, 张永胜, 等.头颈部血管平滑肌瘤[J].中国耳鼻咽喉头颈外科, 2016, 23 (7):377-380.

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    RANJAN S, SINGH K T.Gingival angioleiomyomainfrequent lesion of oral cavity at a rare site[J].J Oral Maxillofac Pathol, 2014, 18:107-110.

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收稿日期:  2018-07-12

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