Peripheral ameloblastoma

  • 文章类型: Case Reports
    未经证实:外周成釉细胞瘤(PA)的发生很少见。二极管激光对PA的切除是不常见的。
    UNASSIGNED:一名27岁女性患者在过去一年中出现无症状的后磨牙三角区肿块。
    未经证实:穿刺活检显示PA侵袭性。
    UNASSIGNED:在局部麻醉下使用二极管激光切除病灶。切除的标本显示了PA棘皮瘤变体的组织病理学特征。
    UNASSIGNED:患者随访两年,无任何复发证据。
    UASSIGNED:二极管激光是传统手术刀切除口腔内软组织病变的一种可接受的替代方法,然而,在PA的情况下,事实证明也不例外。
    UNASSIGNED: Occurrence of peripheral ameloblastoma (PA) is rare. Excision of PA by diode laser is infrequent.
    UNASSIGNED: A 27-year-old female patient presented with an asymptomatic mass on the retromolar trigone for the past one year.
    UNASSIGNED: Incisional biopsy showed aggressive PA.
    UNASSIGNED: The lesion was excised using a diode laser under local anaesthesia. The excised specimen revealed histopathological features of the acanthomatous variant of PA.
    UNASSIGNED: The patient was followed up for two years without any evidence of recurrence.
    UNASSIGNED: Diode laser is an acceptable alternative to conventional scalpel excision for intraoral soft tissue lesions, whereas, in the case of PA, it proves to be no exception.
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  • 文章类型: Case Reports
    成釉细胞瘤是相当常见的牙源性肿瘤,它们可以是骨内或牙龈周围的,这是罕见的发现骨内成釉细胞瘤与牙龈延伸。这里,我们报告了一个40岁的妇女,她在46颗牙齿的牙龈水平出现了外生性牙龈病变,该牙齿在咨询前01年因疼痛而被拔除。临床和放射学检查显示同一区域存在两个肿瘤。患者受益于牙龈肿瘤的切除和骨内肿瘤的摘除。组织病理学和免疫组织化学检查显示,各自的肿瘤是梭形细胞上皮和不同起源的腔内单囊性成釉细胞瘤,留下问题,寻找这两种肿瘤之间的关系。在手术治疗后的12个月随访期间,术后病程顺利。
    Ameloblastomas are quite frequent odontogenic tumors, they can be intraosseous or peripheral to the gum, it\'s rare to find an intraosseous ameloblastoma with gingival extension. Here, we report the case of a 40 years old woman who presented with an exophytic gingival lesion at the gum level of the 46 tooth that was extracted at a quack 01 years before her consultation due to pain in this area. Clinical and radiological examination revealed the presence of two tumors in the same area. The patient benefited from an excision of her gingival tumor and an enucleation of her intraosseous tumor. Histopathological and immunohistochemical examinations revealed that the respective tumors were a spindle cell epulis and an intraluminal unicystic ameloblastoma of different origins, leaving the question and search for the relationship between these two tumors. The postoperative course was uneventful during the 12-month follow-up period after surgical treatment.
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  • 文章类型: Case Reports
    Peripheral ameloblastoma (PA) is a rare benign peripheral odontogenic tumor arising in the gingiva and in the overlying mucosa of tooth-bearing areas of the jaws. Recent data suggestthat the recurrence rate is directly related to inadequate surgical excision. This case of a 71-year-old man reports a poorly delineated mass effecting the gum of the left mandibular canine-premolars area histologically corresponded to PA. In complement to clinical visual examination of such a poorly delineated, non-exophytic and non-dyschromic inflammatory lesion, medical infrared thermography (MIT) - a non-invasive, non-ionizing and real-time imaging technique - was used to optimize the soft tissue margins, and a marginal bone resection was performed. MIT has also been found to be a useful tool in monitoring the absence of diseased tissue crossing the excisional margins at the end of the operation to minimize the risk of recurrence. After two years of follow-up, no local recurrence was found.
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  • 文章类型: Case Reports
    Ameloblastomas are benign epithelial odontogenic neoplasms which are locally aggressive with an insidious growth pattern. Based on the clinical, radiographic, histopathology and behavioral and prognostic aspects, four variants of ameloblastoma are distinguished. They include solid/multicystic ameloblastoma, unicystic ameloblastoma (UA), peripheral ameloblastoma (PA) and desmoplastic ameloblastoma. UA and PA are two variants that have no clinical or radiological resemblance to each other. A case of simultaneous occurrence of these two lesions displaying an array of different histopathological entities together, with a note on pathological insight, has been reported in a 59-year-old adult male patient.
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    文章类型: Case Reports
    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.
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