Suppr超能文献

颅骨原发性成釉细胞瘤的恶性转化:病例报告及当前文献综述

Malignant transformation of primary ameloblastoma of skull: case report and review of current literature.

作者信息

Xu Haitong, Tan Jialiang, Fu Dongxiang

机构信息

Department of Neurosurgery, Guangdong Sanjiu Brain Hospital, Guangzhou, China.

出版信息

Front Oncol. 2024 Mar 21;14:1365625. doi: 10.3389/fonc.2024.1365625. eCollection 2024.

Abstract

BACKGROUND

Since 1964, there has been a scarcity of reported cases of primary ameloblastoma (AM) or ameloblastic carcinoma (AMCa) of the skull. The clinical presentation and distinctive features of this uncommon condition at specific anatomical sites remain unclear. We report a case of malignant transformation of a primary AM of the skull situated in the frontal-temporal-parietal region and highlight its similarities to other cases reported in the literature.

CLINICAL PRESENTATION

A 53-year-old female patient presented with a 20-day history of headaches and bilateral lower limb weakness for 10 days. Physical examination revealed slow and unsteady gait. An occupying lesion was observed in the right frontal-temporal-parietal region of the skull on the Cranial imaging. A right cranial bone tumor margin expansion resection was performed. The patient's motor functions recovered normally after surgery. Postoperative imaging examinations showed10 tumor resection. Follow-up imaging examinations showed tumor recurrence. The patient underwent resection of the recurrent tumor. Postoperative pathological analysis revealed malignant transformation of the AM.Follow-up imaging examinations showed tumor recurrence again. The patient was admitted for stereotactic radiotherapy. Follow-up imaging examinations demonstrated no evidence of tumor recurrence and subsequent chest CT revealed no signs of metastasis.

CONCLUSION

Primary AM or AMCa of the skull is increasingly being described in the literature, but detailed reports on the malignant transformation of primary AM of the skull are lacking. The pathogenesis of this condition remains unclear. Aggressive treatment and close follow-up may be crucial for preventing disease recurrence and malignant transformation.

摘要

背景

自1964年以来,颅骨原发性成釉细胞瘤(AM)或成釉细胞癌(AMCa)的报道病例稀少。这种罕见疾病在特定解剖部位的临床表现和独特特征仍不明确。我们报告一例位于额颞顶区的颅骨原发性AM恶变病例,并强调其与文献中报道的其他病例的相似性。

临床表现

一名53岁女性患者,有20天头痛病史,双侧下肢无力10天。体格检查显示步态缓慢且不稳。头颅影像学检查发现颅骨右额颞顶区有占位性病变。行右颅骨肿瘤边缘扩大切除术。术后患者运动功能恢复正常。术后影像学检查显示肿瘤切除。随访影像学检查显示肿瘤复发。患者接受复发性肿瘤切除术。术后病理分析显示AM恶变。随访影像学检查再次显示肿瘤复发。患者入院接受立体定向放射治疗。随访影像学检查未发现肿瘤复发迹象,随后胸部CT显示无转移迹象。

结论

文献中对颅骨原发性AM或AMCa的描述越来越多,但缺乏关于颅骨原发性AM恶变的详细报道。这种疾病的发病机制仍不清楚。积极治疗和密切随访对于预防疾病复发和恶变可能至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ff9/10991779/7d618b68d2b1/fonc-14-1365625-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验