首页> 外文期刊>Journal of Oral and Maxillofacial Surgery >Multiple myeloma presenting as mandibular ill-defined radiolucent lesion with numb chin syndrome: a case report.
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Multiple myeloma presenting as mandibular ill-defined radiolucent lesion with numb chin syndrome: a case report.

机译:多发性骨髓瘤表现为下颌不明确的放射线透明病变伴麻木下巴综合征:一例病例报告。

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摘要

Multiple myeloma is a malignant neoplasm of plasma cells that is characterized by the production of pathologic M proteins, bone lesions, kidney disease, hyperviscosity, and hypercalcemia. Human leukocyte antigen studies suggest a genetic predisposition to the disease, which occurs equally in both genders, most often in patients aged older than 50 years. Anemia and skeletal pain are the most common presenting symptoms, and bone pain is caused by bone lysis that may result either directly from accumulation of tumor cells or indirectly from osteoclast-activating factors secreted by the malignant myeloma cells. Multiple myeloma manifestations of the head and neck are common but usually occur in the late stages of the disease; mandibular involvement with multiple myeloma as the initial presenting sign of the disease is extremely rare. In this case report we present a unique case of multiple myeloma with mandibular radiolucent lesion as the first sign of the disease.
机译:多发性骨髓瘤是浆细胞的恶性肿瘤,其特征在于产生病理性M蛋白,骨骼损伤,肾脏疾病,高粘度和高钙血症。人类白细胞抗原研究表明,这种疾病的遗传易感性,男女均相同,多数情况下年龄超过50岁。贫血和骨骼疼痛是最常见的症状,骨骼疼痛是由骨溶解引起的,其可能直接由肿瘤细胞的积累引起,也可能由恶性骨髓瘤细胞分泌的破骨细胞活化因子间接引起。头颈部多发性骨髓瘤表现很常见,但通常发生在疾病的晚期。下颌累及多发性骨髓瘤是该病的最初表现,极为罕见。在本病例报告中,我们介绍了一个独特的多发性骨髓瘤病例,其下颌放射线透明病变是该疾病的首发征兆。

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