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颗粒细胞型成釉细胞瘤病例报告——一种罕见的组织学类型。

A case report on granular cell ameloblastoma - A rare histological entity.

作者信息

Mathew Anju

机构信息

Senior Lecturer, Oral Medicine and Radiology, Pushpagiri College of Dental Sciences, Perumthuruthy, Thiruvalla, Kerala, India.

出版信息

Indian J Radiol Imaging. 2020 Apr-Jun;30(2):225-228. doi: 10.4103/ijri.IJRI_145_19. Epub 2020 Jul 13.

Abstract

Granular cell ameloblastoma is a rare condition, accounting for 3.5% of all ameloblastoma cases that shows marked transformation in the cytoplasm of tumor cells, which are usually stellate reticulum-like cells. The transformed cells possess very coarse, granular eosinophilic cytoplasm. Granular cell ameloblastoma is aggressive in nature with a marked propensity for recurrence and can progress to metastasis. This article discusses a case report of a 35-year-old female patient diagnosed with granular cell ameloblastoma of the right mandible.

摘要

颗粒细胞成釉细胞瘤是一种罕见疾病,占所有成釉细胞瘤病例的3.5%,其肿瘤细胞(通常为星网状样细胞)的细胞质有明显改变。转化后的细胞具有非常粗糙的、嗜酸性颗粒状细胞质。颗粒细胞成釉细胞瘤本质上具有侵袭性,有明显的复发倾向,且可进展为转移。本文讨论了一例35岁女性患者被诊断为右下颌骨颗粒细胞成釉细胞瘤的病例报告。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dad4/7546283/bc1d8baf2eb7/IJRI-30-225-g001.jpg

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