左舌下腺原发性成釉细胞瘤1例报告
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摘要
本文报告1例原发于舌下腺的成釉细胞瘤患者。查体见该患者左侧口底相当于左舌下腺区一卵圆形肿物,影像学检查显示肿物位于左舌下腺区,未侵及下颌骨,上、下颌颌骨无明显异常。完善术前检查,明确无绝对禁忌证后手术治疗。组织学检查显示肿物与舌下腺密切相关,且符合成釉细胞瘤病理表现。术后7 d患者伤口愈合良好出院,术后随访5个月肿瘤无复发。
This paper described a patient who suffered from ameloblastoma in the sublingual gland. Clinical examination found an oval-shaped mass in the left floor of the mouth. Imaging examination revealed that the mass located in the left sublingual gland area and did not invade the mandible. Preoperative examinations confirmed that there were no surgical contraindications, then surgical removal of the tumor was performed, and there was no evidence of recurrence 5 months after surgery. Histological examination showed that the tumor was closely related to the sublingual gland, the final pathologic diagnosis was peripheral ameloblastoma.
This paper described a patient who suffered from ameloblastoma in the sublingual gland. Clinical examination found an oval-shaped mass in the left floor of the mouth. Imaging examination revealed that the mass located in the left sublingual gland area and did not invade the mandible. Preoperative examinations confirmed that there were no surgical contraindications, then surgical removal of the tumor was performed, and there was no evidence of recurrence 5 months after surgery. Histological examination showed that the tumor was closely related to the sublingual gland, the final pathologic diagnosis was peripheral ameloblastoma.
引文
[1]Philipsen HP,Reichart PA,Nikai H,et al.Peripheral ameloblastoma:biological profile based on 160 cases from the literature[J].Oral Oncol,2001,37(1):17-27.
[2]Braunstein E.Case report of an extraosseous adamantoblastoma[J].Oral Surg Oral Med Oral Pathol,1949,2(6):726-728.
[3]Klinar KL,McManis JC.Soft-tissue ameloblastoma.Report of a case[J].Oral Surg Oral Med Oral Pathol,1969,28(2):266-272.
[4]Ramnarayan K,Nayak RG,Kavalam AG.Peripheral ameloblastoma[J].Int J Oral Surg,1985,14(3):300-301.
[5]Woo SB,Smith-Williams JE,Sciubba JJ,et al.Peripheral ameloblastoma of the buccal mucosa:case report and review of the English literature[J].Oral Surg Oral Med Oral Pathol,1987,63(1):78-84.
[6]Shibata T,Kaneko N,Hokazono K,et al.An ameloblastoma-like neoplasm of the buccal mucosa.Report of a case[J].Int J Oral Maxillofac Surg,1990,19(4):203-204.
[7]Yamanishi T,Ando S,Aikawa T,et al.A case of extragingival peripheral ameloblastoma in the buccal mucosa[J].J Oral Pathol Med,2007,36(3):184-186.
[8]Isomura ET,Okura M,Ishimoto S,et al.Case report of extragingival peripheral ameloblastoma in buccal mucosa[J].Oral Surg Oral Med Oral Pathol Oral Radiol Endod,2009,108(4):577-579.
[9]Goda H,Nakashiro K,Ogawa I,et al.Peripheral ameloblastoma with histologically low-grade malignant features of the buccal mucosa:a case report with immunohistochemical study and genetic analysis[J].Int J Clin Exp Pathol,2015,8(2):2085-2089.
[10]单一旦,王国云.骨成釉细胞瘤的组织起源[J].国际口腔医学杂志,2006,33(4):272-274.
[11]Califano L,Naremonti P,Boscaino A,et al.Peripheral ameloblastoma:report of a case with malignant aspect[J].Br JOral Maxillofac Surg,1996,34(3):240-242.
[2]Braunstein E.Case report of an extraosseous adamantoblastoma[J].Oral Surg Oral Med Oral Pathol,1949,2(6):726-728.
[3]Klinar KL,McManis JC.Soft-tissue ameloblastoma.Report of a case[J].Oral Surg Oral Med Oral Pathol,1969,28(2):266-272.
[4]Ramnarayan K,Nayak RG,Kavalam AG.Peripheral ameloblastoma[J].Int J Oral Surg,1985,14(3):300-301.
[5]Woo SB,Smith-Williams JE,Sciubba JJ,et al.Peripheral ameloblastoma of the buccal mucosa:case report and review of the English literature[J].Oral Surg Oral Med Oral Pathol,1987,63(1):78-84.
[6]Shibata T,Kaneko N,Hokazono K,et al.An ameloblastoma-like neoplasm of the buccal mucosa.Report of a case[J].Int J Oral Maxillofac Surg,1990,19(4):203-204.
[7]Yamanishi T,Ando S,Aikawa T,et al.A case of extragingival peripheral ameloblastoma in the buccal mucosa[J].J Oral Pathol Med,2007,36(3):184-186.
[8]Isomura ET,Okura M,Ishimoto S,et al.Case report of extragingival peripheral ameloblastoma in buccal mucosa[J].Oral Surg Oral Med Oral Pathol Oral Radiol Endod,2009,108(4):577-579.
[9]Goda H,Nakashiro K,Ogawa I,et al.Peripheral ameloblastoma with histologically low-grade malignant features of the buccal mucosa:a case report with immunohistochemical study and genetic analysis[J].Int J Clin Exp Pathol,2015,8(2):2085-2089.
[10]单一旦,王国云.骨成釉细胞瘤的组织起源[J].国际口腔医学杂志,2006,33(4):272-274.
[11]Califano L,Naremonti P,Boscaino A,et al.Peripheral ameloblastoma:report of a case with malignant aspect[J].Br JOral Maxillofac Surg,1996,34(3):240-242.