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Sinonasal ameloblastoma: A case report focusing on histogenesis and related morphological characteristics

机译:Sinonasal Ameloblastoma:一种案例报告,重点是组织生理学和相关形态特征

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Sinonasal ameloblastoma is an extremely rare neoplasm. Herein we present a case of sinonasal ameloblastoma and discuss its histogenesis and related morphological characteristics. An 80 years-old Japanese male had a polypoid mass initially diagnosed as a nasal polyp. A prior biopsy was interpreted as a salivary gland-type tumor and he was therefore referred to a regional general hospital for surgical removal of the lesion. Preoperative contrast-enhanced magnetic resonance imaging revealed a space-occupying lesion in the right nasal cavity and the right maxillary sinus with poor contrast enhancement. Histopathological findings revealed that the tumor consisted of follicular/plexiform-like cell nests with peripheral palisading, extending continuously to the adjacent mucosa. A recurrent polypoid mass accompanied by bone destruction of the maxillary sinus was found two years after the surgery, but it was left untreated. Although sinonasal ameloblastoma remains under-recognized, its characteristics, including its histopathological features, need to be more widely known to allow its correct diagnosis and adequate management.
机译:Sinonasal Ameloblastoma是一个极其稀有的肿瘤。在此,我们提出了Sinonasal Ameloblastoma的情况,并讨论其组织发生和相关形态特征。一个80岁的日本男性有息肉质量最初被诊断为鼻息肉。以前的活检被解释为唾液腺型肿瘤,因此他被称为区域综合医院,用于手术去除病变。术前对比度增强的磁共振成像显示出右侧鼻腔和右上颌窦的空间占据病变,其对比度增强差。组织病理学发现揭示了肿瘤由具有外周调出的卵泡/斑块状的细胞巢组成,连续向相邻的粘膜延伸。在手术后两年发现伴有上颌窦的骨破坏的复杂息肉质量,但它被留下了未经处理。虽然Sinonasal Ameloblastoma仍然不公认,但其特征包括其组织病理学特征,需要更广为人知,允许其正确的诊断和适当的管理。

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