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Multiple congenital oral granular cell tumours in a newborn black female: a case report

机译:新生儿黑人女性多发性先天性口腔颗粒细胞瘤1例

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Introduction Congenital oral granular cell tumour of the newborn is an uncommon benign tumour of uncertain origin. The typical clinical appearance is of a single nodule occurring on the anterior maxillary ridge. In 10% of cases there are multiple lesions. The occurrence of congenital epulis in non-Caucasians is rare. Case presentation Two firm pedunculated nodular lesions were noticed in the mouth of a 3-day-old black female: one on the anterior maxillary ridge and the other further posteriorly in the midline of the palate. Both lesions were excised when the baby was nine days old. Microscopic examination of the lesions showed densely packed round to oval cells with abundant granular eosinophilic cytoplasm and uniform nuclei. The diagnosis was congenital granular cell tumour. Conclusion Congenital oral granular cell tumour occurs almost exclusively in Caucasian newborns but also rarely in black infants. The parents should be assured of the benign nature and the simple treatment of the condition.
机译:引言新生儿先天性口腔颗粒细胞瘤是一种来源不明的罕见良性肿瘤。典型的临床表现是上颌前terior上出现单个结节。在10%的病例中有多个病变。在非高加索人中,先天性ep骨的发生很少。病例介绍一名三天大的黑人女性的嘴中发现了两个牢固的带蒂结节性病变:一个位于上颌前ridge,另一个位于上the中线。婴儿九天大时,两个病变都被切除。病变的显微镜检查显示,卵圆形细胞密集地包裹着,具有丰富的嗜酸性粒细胞质和均匀的细胞核。诊断为先天性粒细胞瘤。结论先天性口腔颗粒细胞瘤几乎只发生在白种人新生儿中,但很少发生在黑人婴儿中。应该确保父母的良性和对疾病的简单治疗。

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