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颌骨颗粒细胞成釉细胞瘤。两例细针穿刺细胞学报告。

Granular cell ameloblastoma of the jaw. A report of two cases with fine needle aspiration cytology.

作者信息

Deshpande A, Umap P, Munshi M

机构信息

Department of Pathology, Government Medical College, Nagpur, Maharashtra, India.

出版信息

Acta Cytol. 2000 Jan-Feb;44(1):81-5. doi: 10.1159/000326231.

Abstract

BACKGROUND

Fine needle aspiration cytology (FNAC) of jaw tumors has not been studied extensively. Ameloblastomas are jaw tumors that show a wide morphologic spectrum and thus may pose some diagnostic difficulties. Of the many types, granular cell ameloblastoma (GCA) is an uncommon variant that possesses distinctive features. To the best of our knowledge, there have been no previous reports on the cytologic findings of GCA. We present two cases diagnosed by FNAC.

CASES

Two cases of GCA were diagnosed on cytology and subsequently confirmed on histology. Both patients presented with a large, lytic jaw tumor. FNAC smears showed characteristic granular cells along with spindle and basaloid cells.

CONCLUSION

Although GCAs are rare tumors, they possess distinctive features that permit an accurate diagnosis, provided that this entity is kept in mind. This tumor has to be differentiated from cystic odontogenic lesions, epulis and granular cell myoblastoma. An accurate preoperative diagnosis also helps the surgeon to plan more extensive surgery as these tumors show a great propensity for malignant change and metastases.

摘要

背景

颌骨肿瘤的细针穿刺细胞学检查(FNAC)尚未得到广泛研究。成釉细胞瘤是一种颌骨肿瘤,其形态谱广泛,因此可能存在一些诊断困难。在众多类型中,颗粒细胞成釉细胞瘤(GCA)是一种具有独特特征的罕见变体。据我们所知,此前尚无关于GCA细胞学表现的报道。我们报告两例经FNAC诊断的病例。

病例

两例GCA经细胞学诊断,随后经组织学证实。两名患者均表现为颌骨的巨大溶骨性肿瘤。FNAC涂片显示特征性的颗粒细胞以及梭形细胞和基底样细胞。

结论

尽管GCA是罕见肿瘤,但只要考虑到这一实体,它们具有可准确诊断的独特特征。该肿瘤必须与囊性牙源性病变、龈瘤和颗粒细胞成肌细胞瘤相鉴别。准确的术前诊断也有助于外科医生规划更广泛的手术,因为这些肿瘤具有很高的恶变和转移倾向。

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