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气道神经鞘瘤1例

Primary tracheal neurilemmoma:one case report
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摘要 目的提高对气道神经鞘瘤的认识,减少对该病的误诊和漏诊。方法回顾我院收治的1例气道神经鞘瘤患者的病历资料,探讨对该病的诊断及病变特点。结果患者反复活动后气促1年,肺功能正常,胸部CT提示气道肿物。气管镜活检病理示气道慢性炎症。气管切开行肿物消融术,病理诊断为神经鞘瘤。结论气道神经鞘瘤临床表现不特异,不易早期诊断,临床易漏诊延误诊断,手术切除仍是治疗气道神经鞘瘤最有效的方法。 Objective To further investigate the pathogenesis of neurilemmoma and avoid misdiagnosis of neurilemmoma. Methods One case of tracheal neurilemmoma was reported, the diagnosis and features of neurilemmoma were discussed. Results The clinical manifestation of the patient was repeated shortness of breath after activities for one year. Lung function was normal. Chest CT showed airway tumor. Bronchoscopy biopsy revealed chronic airway inflammation. Tumor ablation was made after incision of trachea, pathological diagnosis result was neurilemmoma. Conclusions There are little of typical symptoms in neurilemmomas so that it is difficult to make early diagnosis, misdiagnosis always happens. Surgical resection is effective in the treatment of tracheal schwannoma.
出处 《国际呼吸杂志》 2016年第11期837-839,共3页 International Journal of Respiration
关键词 神经鞘瘤 气道 误诊 Neurilemrnoma Trachea Misdiagnosis
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  • 1Wolters PL, Martin S, Merker VL, et al. Patient-reported outcomes in neurofibromatosis and schwannomatosis clinical trials[J]. Neurology, 2013,81 (21) : $6-14. DOI: 10. 1212/01. wnl. 0000435747. 02780. bf. 被引量:1
  • 2Veno S, Duvnjak S, Eekardt J. Primary benign schwanomma in trachea[J]. Ugeskr Laeger, 2013,175(21) :1501-1502. 被引量:1
  • 3Kleihues P, Louis DN, Scheithauer BW, et al. The WHO classification of tumors of the nervous system [J]. J Neuropathol Exp Neurol, 2002, 61 (3): 215-229. DOI: 10. 1093/jnen/61.3. 215. 被引量:1
  • 4Uhlmann EJ, Plotkin SR. Neurofibromatoses [J]. Adv Exp Med Biol, 2012, 724: 266-277. DOI: 10. 1007/978-1-4614- 0653-2_20. 被引量:1
  • 5Smith MJ, Walker JA, Shen Y, et al. Expression of SMARCB1 (INI1) mutations in familial schwannomatosis [J]. Hum Mol Genet, 2012, 21 (24): 5239-5245. DOI: 10. 1093/hmg/dds370. 被引量:1
  • 6Asai K, Tani S, Mineharu Y, et al. Familial sehwannomatosis with a germline mutation of SMARCB1 in Japan [J]. Brain Tumor Pathol, 2015, 32 (3) :216-220. DOI: 10. 1007/s10014- 015-0213-9. 被引量:1
  • 7MacCollin M, Chiocca EA, Evans DG, et al. Diagnostic criteria for sehwannomatosis [J]. Neurology, 2005, 64 ( 11 ) : 18a8- 1845. 被引量:1
  • 8Le Rouzic O, Ramon PP, Bouchindhomme B, et al. Benign trachobronchial schwannoma treated by complete endoscopic resection followed by cryotherapy[J]. Rev Mal Respir, 2011, 28(1) :88-91.DOI:10. 1016/j.rmr. 2010.05.018. 被引量:1

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