Otto Mario, Shulkin Barry L, Kundu Mondira, Sandlund John T, Snyder Scott E, Metzger Monika L
Department of Oncology, St Jude Children's Research Hospital, Memphis, TN, USA.
J Pediatr Hematol Oncol. 2012 Apr;34(3):232-5. doi: 10.1097/MPH.0b013e3182281c54.
Inflammatory pseudotumors (IPTs) are rare, enigmatic lesions that may develop as a late manifestation of a reparative process. We describe the case of a teenager with primary mediastinal subtype of diffuse large B-cell lymphoma who developed an IPT at the site of the original lymphoma, mimicking relapse of disease on positron emission tomography/computed tomography imaging. This is the first report of IPT in a teenager with mediastinal lymphoma. This case is an important reminder of the limitations of positron emission tomography/computed tomography imaging in patients with lymphoma and stresses the importance of histologic confirmation of suspected treatment failure or relapse.
炎性假瘤(IPTs)是罕见的、难以解释的病变,可能作为修复过程的晚期表现而出现。我们描述了一例弥漫性大B细胞淋巴瘤原发性纵隔亚型的青少年病例,该患者在原淋巴瘤部位出现了炎性假瘤,在正电子发射断层扫描/计算机断层扫描成像上表现为疾病复发。这是青少年纵隔淋巴瘤患者中炎性假瘤的首例报告。该病例有力地提醒了淋巴瘤患者正电子发射断层扫描/计算机断层扫描成像的局限性,并强调了对疑似治疗失败或复发进行组织学确认的重要性。