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Primary Maxillofacial Large B-Cell Lymphoma in Immunocompetent Patients: Report of 5 Cases

机译:免疫功能正常的原发性颌面部大B细胞淋巴瘤5例报告

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摘要

Lymphomas of the oral cavity represent 5% of all lymphomas. They usually occur in immunocompromised patients. Lymphoma arising within a single bone, without visceral or lymph node involvement, is known as primary intraosseous lymphoma. It is a rare condition and constitutes 3.1% of malignant bone tumors and 5% of extranodal lymphomas. Primary lymphoma of the jaw is seldom seen and it is often misdiagnosed. Clinically, the manifestations are usually similar to an odontogenic tumor, cyst, or infection. Radiographically it appears as a radiolucent area that may mimic endodontic lesion, periodontal pathology, or odontogenic cyst or tumor. The initial presentation is commonly followed by multiple unnecessary extractions and/or root canal treatments. We present five cases of rare primary lymphoma of the maxillofacial complex, four of them intraosseous.
机译:口腔淋巴瘤占所有淋巴瘤的5%。它们通常发生在免疫功能低下的患者中。在没有内脏或淋巴结累及的情况下,单个骨骼内产生的淋巴瘤被称为原发性骨内淋巴瘤。它是一种罕见病,占恶性骨肿瘤的3.1%和结外淋巴瘤的5%。很少见到下颌原发性淋巴瘤,并且经常被误诊。临床上,这些表现通常类似于牙源性肿瘤,囊肿或感染。影像学上它表现为射线可透区域,可模仿牙髓病变,牙周病理或牙源性囊肿或肿瘤。最初的表现通常是在进行多次不必要的拔牙和/或根管治疗之后。我们介绍了5例罕见的颌面部复杂原发性淋巴瘤,其中4例为骨内性。

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