Vasudevan Vijeev, Kumar Yella Ravi, Chavva Prathyusha, Naina S
Department of Oral Medicine and Radiology, Krishnadevaraya College of Dental Sciences, Bengaluru, Karnataka, India.
Indian J Dent Res. 2016 May-Jun;27(3):334-8. doi: 10.4103/0970-9290.186229.
Plasmablastic Lymphoma of oral cavity is an aggressive rare form of Non Hodgkin's Lymphoma which is an Acquired Immuno Deficiency Syndrome defining condition. Head and neck region is the second most common area for extranodal NHL's primarily involving gingiva and palate, which often presents as a diagnostic problem. We report a case of PBL in a 19 year old female patient later diagnosed as Human Immunodeficiency Virus (HIV) positive. She presented with expanding painful ulceroproliferative lesion involving left mandible and gingiva of 20 days duration. Histopathological examination and immunohistochemical analysis confirmed the diagnosis. Uncommon discovery of multiple bony lesions in whole body CT and hypercalcemia raise a question about Multiple Myeloma (MM). Literature showed very few cases with osteolytic lesions and none of the cases reported multiple bone lesions in skull. Our case report stresses the importance of differentiating this extremely rare case of PBL with skull lesions from MM.
口腔浆母细胞淋巴瘤是一种侵袭性的罕见非霍奇金淋巴瘤,是获得性免疫缺陷综合征的定义性病症。头颈部是结外非霍奇金淋巴瘤的第二常见部位,主要累及牙龈和腭部,这常常带来诊断难题。我们报告一例19岁女性浆母细胞淋巴瘤患者,该患者后来被诊断为人类免疫缺陷病毒(HIV)阳性。她表现为累及左下颌骨和牙龈的进行性疼痛性溃疡增生性病变,病程20天。组织病理学检查和免疫组化分析确诊了该病例。全身CT发现罕见的多处骨质病变以及高钙血症引发了关于多发性骨髓瘤(MM)的疑问。文献显示溶骨性病变的病例极少,且没有病例报告颅骨出现多处骨质病变。我们的病例报告强调了将这种极为罕见的伴有颅骨病变的浆母细胞淋巴瘤病例与多发性骨髓瘤相鉴别的重要性。