颗粒细胞瘤(Abrikossoff肿瘤):病例系列

Maria Regina Sposto , Cláudia Maria Navarro , Cleverton Roberto de Andrade
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引用次数: 30

摘要

本病例系列描述了三例未报道的罕见良性肿瘤,称为Abrikossoff肿瘤或颗粒细胞瘤(GCT)。这种间充质肿瘤明显起源于神经细胞或雪旺细胞,有良恶性两种形式。本文报告的所有病例均为口腔黏膜上独特的结节,来自结缔组织,发生于30至42岁的女性。GCT组织学显示大颗粒细胞成组排列,结缔组织巢状细胞分离假上皮瘤覆盖表面。这一特征可能被误解为鳞状细胞癌。恶性和良性GCT的区分是通过转移的存在来评估的,转移被认为是恶性肿瘤的唯一可靠标准。
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Granular cell tumour (Abrikossoff’s tumour): Case series

This case series describes three unreported cases of an uncommon benign neoplasm named Abrikossoff’s tumour or granular cell tumour (GCT). This mesenchymal neoplasm apparently arises from neural or Schwann cell origin with benign and malignant forms. All cases presented here were unique nodules on oral mucosa, coming out from the connective tissue, and occurring in women with age ranging from 30 to 42 years. The histological aspects of the GCT showed large granular cells arranged in groups and nests of connective tissue separating pseudoepitheliomatous overlying surface. This feature can possibly be misunderstood with squamous cell carcinoma. The differentiation between malignant and benign GCT is evaluated by the presence of metastases which is considered the only reliable criterion for malignancy.

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