Poljak Nikola Kolja, Kljajić Zlatko, Petricević Josko, Forempoher Gea, Simunić Marina Maras, Colović Zavisa, Kontić Mirko
University of Split, Split University Hospital Center, Department of Otorhinolaryngology, Split, Croatia.
Coll Antropol. 2013 Mar;37(1):301-4.
We report an extremely rare case and localization of polypoid angiomiofibroblastoma tumour, a case report and review of the world literature concerning angiomiofibroblastoma tumour. We present the case of a 74-year-old man who underwent left anterior and posterior ethmoidectomy with extirpation of tumour mass from left nasal cavity, epipharinx and left sphenoid sinus. The prognosis for this group of tumour is good and patient didn't receive any kind of therapy except surgical treatment. To our knowledge, this is a rare report in the world literature of polypoid angiomiofibroblastoma tumour of nasal cavity. This case indicates that angiomiofibroblastoma tumour of nasal cavity and paranasal sinuses is a rare disease including its localisation which otolaryngologists should be aware of and one which should be included in the differential diagnosis of tumours involving sinonasal tract.
我们报告了一例极其罕见的息肉样血管黏液纤维瘤病例及肿瘤定位，这是一篇关于血管黏液纤维瘤的病例报告并对世界文献进行了综述。我们呈现了一名74岁男性的病例，该患者接受了左前、后筛窦切除术，并从左鼻腔、鼻咽部和左蝶窦切除肿瘤肿块。这类肿瘤的预后良好，除手术治疗外，患者未接受任何其他治疗。据我们所知，这是世界文献中关于鼻腔息肉样血管黏液纤维瘤的罕见报告。该病例表明，鼻腔及鼻窦的血管黏液纤维瘤是一种罕见疾病，包括其定位，耳鼻喉科医生应予以关注，且应将其纳入鼻窦道相关肿瘤的鉴别诊断中。
