Goda Hiroyuki, Nakashiro Kohichi, Ogawa Ikuko, Takata Takashi, Hamakawa Hiroyuki
Department of Oral and Maxillofacial Surgery, Ehime University Graduate School of Medicine Ehime, Japan.
Center of Oral Clinical Examination, Hiroshima University Hospital Hiroshima, Japan.
Int J Clin Exp Pathol. 2015 Feb 1;8(2):2085-9. eCollection 2015.
Peripheral ameloblastoma (PA), a rare and unusual variant of odontogenic tumors, comprises about 1% of all ameloblastomas. PA is an exophytic growth localized to the soft tissues overlying the tooth-bearing areas of the jaws, and the initial diagnosis is often fibrous epulis. PA with histologically low-grade malignant features is extremely rare. We report a case of peripheral ameloblastoma with histologically low-grade malignant features in a 69-year-old woman that presented with a hemorrhage from a tumor on the right buccal mucosa. The tumor was surgically removed by blunt dissection, with no evidence of recurrence after two years and six months. After the case presentation, microscopic and genetic findings are discussed.
外周型成釉细胞瘤(PA)是一种罕见且特殊的牙源性肿瘤变体,约占所有成釉细胞瘤的1%。PA是一种外生性生长,局限于颌骨牙列区上方的软组织,最初诊断常为纤维性龈瘤。具有组织学低级别恶性特征的PA极为罕见。我们报告一例69岁女性外周型成釉细胞瘤,具有组织学低级别恶性特征,表现为右侧颊黏膜肿瘤出血。肿瘤通过钝性分离手术切除,术后两年零六个月无复发迹象。病例报告后,对微观和基因发现进行了讨论。