Dentinogenic Ghost Cell Tumor: A Rare Case Report in Maxillary Sinus

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Abstract

Ghost Cell Tumors (GCT) are a class of lesions that can exist in the form of a cyst or solid neoplastic tumor, and in terms of behavior, they can be benign, locally invasive, or metastatic. They are identified by the presence of ame-loblastic epithelium, ghost cell, and calcification. These lesions are mostly prevalent in the lower jaw, anterior mandible area. They are distributed equally between the male and female population in the second, sixth, and eighth decades of life. Since the recurrence rate is very low, it seems that a conservative approach is sufficient for most cases. Here, we present a rare case of dentinogenic ghost cell tumor in the left sinus of a 32-year-old male patient. It is temporarily diagnosed through clinical findings and .radiographic scan, and later on, confirmed via histology
上颌窦牙本质源性鬼细胞瘤1例
鬼细胞瘤(Ghost Cell Tumors, GCT)是一类以囊肿或实体性肿瘤形式存在的病变,从行为上看,它们可以是良性的、局部侵袭性的或转移性的。它们可以通过母细胞上皮、鬼影细胞和钙化来鉴别。这些病变多见于下颚、下颌骨前部。在人生的第二、第六和第八个十年,它们在男性和女性之间平均分布。由于复发率很低,似乎保守的方法是足够的,对大多数情况下。在此,我们报告一个罕见的32岁男性左鼻窦牙本质源性鬼细胞肿瘤病例。它是通过临床表现和x线扫描暂时诊断出来的,后来通过组织学证实
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