Gupta S C, Tewarson S L, Malhotra M
Dept. Of ENT, S.R.N. Hospital, M.L.N. Medical College, 211 002 Allahabad, India.
Indian J Otolaryngol Head Neck Surg. 2006 Apr;58(2):196-8. doi: 10.1007/BF03050789.
Maxillary sinus is a rare site for the occurrence of haemangioendothelioma. The present case is being reported in a 45 year old Hindu Male. The main complaint ware bilateral nasal obstruction und a mass protruding from he right nostril along with episodes of headache, vomiting and nasal bleeding. The. C.T. scan showed evidence of erosion of bony walls of maxillary antrum with intracranial extension of the tumor. There was no evidence of regional lymph nodes or distance metastasis. Histology of the tissue revealed a highly cellular and vascular tumor the diagnosis of haemangioendothelioma of the maxillary sinus retiform variety was established.
上颌窦是血管内皮瘤发生的罕见部位。本病例报告的是一名45岁的印度教男性。主要症状为双侧鼻塞、右鼻孔有肿物突出,伴有头痛、呕吐和鼻出血。CT扫描显示上颌窦骨壁有侵蚀,肿瘤向颅内扩展。没有区域淋巴结或远处转移的证据。组织学检查显示为高度细胞性和血管性肿瘤,确诊为上颌窦网状型血管内皮瘤。