Paraganglioma of maxillary sinus associated with Addison’s disease mimicking a vascular tumour: A case report

Sami A Alkindy
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引用次数: 1

Abstract

Paraganglioma of the nasal and paranasal sinuses are quite rare neuroendocrine tumours, usually hormonally inactive, presentingas nasal polyps with or without epistaxis. We present a rare case of a 23 year old male, with Addison’s disease, who was referredfrom endocrinology department with a complaint of right nasal blockage associated with recurrent epistaxis. A provisionalclinical diagnosis of vascular tumour was made, Computed tomography and MRI suggested hemangioma /inverted papilloma.However, biopsy reported a highly vascular tissue mimicking angiofibroma, further immunostaining studies with Synaptophysinand S-100 confirmed the diagnosis of Paraganglioma. This rare tumour in the paranasal sinuses may mimic vascular tumour andcan only be confirmed with histopathological immunostains studies. According to our knowledge, this is first case reported to beassociated with Addison’s disease in the English literature.
上颌窦副神经节瘤合并Addison病(血管性肿瘤)1例
鼻窦和副鼻窦神经节瘤是一种罕见的神经内分泌肿瘤,通常为激素活性低下,表现为鼻息肉,伴或不伴鼻出血。我们报告一例罕见的23岁男性艾迪生病患者,从内分泌科转诊,主诉右鼻阻塞伴复发性鼻出血。初步临床诊断为血管瘤,ct及MRI提示为血管瘤/内翻性乳头状瘤。然而,活检报告了高度血管性组织模拟血管纤维瘤,进一步用synaptophysin和S-100免疫染色研究证实了副神经节瘤的诊断。这种罕见的肿瘤发生在鼻窦,可能与血管肿瘤相似,只能通过组织病理学免疫染色研究来证实。据我们所知,这是英国文献中第一例与艾迪生病相关的病例。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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