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Malignant ameloblastoma in an 8-year-old child with metastasis to the lung: case report with a clinicopathologic analysis

机译:一名8岁儿童转移至肺部的恶性成釉细胞瘤:病例报告及临床病理分析

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Ameloblastomas are rare tumors of odontogenic origin, accounting for 1% of all oral tumors. They are benign, but locally highly aggressive tumors. We report here the unusual case of an 8-year-old patient with multicystic mandibular ameloblastoma, who was submitted to surgery for two relapses in six years and metastasized to the lung two years after initial surgery. The first lesion, diagnosed as follicular ameloblastoma, was treated conservatively with enucleation and curettage. Two years later the tumor relapsed into multicystic granular form. A marginal conservative resection was performed, keeping the basilar contour of the mandible, due to the age of the patient. Three months later, on a routine follow-up examination, a lung metastasis was detected with no signs of tumor in the mandibular bone and the patient was submitted to upper right lobectomy. Three years later a new recurrent tumor was detected in the alveolar process and another marginal resection was performed. Histologically, the tumor showed the follicular growth pattern. After a disease-free period of over five years, the patient was again submitted to surgery for mandibular reconstruction. The mandibular bony defect was filled with iliac bone blocks and four dental implants. He underwent oral rehabilitation with an implant-supported overdenture. With a follow-up period of 22 years since first surgery, the patient is currently free of disease.
机译:成釉细胞瘤是牙源性起源的罕见肿瘤,占所有口腔肿瘤的1%。它们是良性的,但局部高度侵袭性的肿瘤。我们在这里报告了8例多囊下颌成纤维细胞瘤患者的不寻常病例,该患者在六年内接受了两次手术复发,并在初次手术后两年转移到肺部。第一个病变被诊断为滤泡性成釉细胞瘤,采用摘除术和刮除术保守治疗。两年后,肿瘤复发为多囊性颗粒状。由于患者的年龄,进行了边缘保守性切除,保留了下颌骨的基底轮廓。三个月后,在常规的随访检查中,检测到肺转移,下颌骨中无肿瘤迹象,患者被送至右上叶切除术。三年后,在肺泡过程中发现了新的复发性肿瘤,并进行了另一次边缘切除。在组织学上,肿瘤显示出卵泡生长模式。经过五年的无病期后,患者再次接受下颌骨重建手术。下颌骨缺损充满了bone骨骨块和四个牙科植入物。他接受了植入物支持的覆盖义齿的口腔修复。自首次手术以来的22年随访期,患者目前没有疾病。

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