Tateishi Ukihide, Terauchi Takashi, Inoue Tomio, Tobinai Kensei
Department of Radiology, Yokohama City University Graduate School of Medicine, Yokohama, Kanagawa, Japan.
Abdom Imaging. 2010 Apr;35(2):232-40. doi: 10.1007/s00261-009-9516-9. Epub 2009 Apr 16.
Nodal involvement of abdominal lymphatic pathways occurs in a number of histologic subtypes of malignant lymphoma. The histologic diagnosis of abnormal uptake in abdominal lymphatic pathways includes mainly non-Hodgkin lymphoma with B-cell lineage and Hodgkin lymphoma. Initial involvement of pelvic and retroperitoneal lymphatic pathways can result from a variety of underlying non-Hodgkin's lymphoma: follicular lymphoma, diffuse large B-cell lymphoma, marginal zone B-cell lymphoma of mucosa-associated lymphoid tissue (MALT) type, and mantle cell lymphoma. The diagnosis of these clinical entities requires various imaging techniques, including fluorine-18-fluorodeoxyglucose ((18)FDG) positron emission tomography/computed tomography (PET/CT), computed tomography, (67)Gallium scintigraphy, and magnetic resonance imaging (MRI). Specific symptoms of these diseases are often lacking, but intense (18)FDG accumulation on PET/CT may be a marker of disease activity. Interpretation of the presence of and the specific pattern of (18)FDG uptake may obviate the need for invasive biopsy. However, distinction of abnormal uptake is often difficult to determine because focal accumulation of (18)FDG in the urinary tract or intestine mimics nodal involvement in the pelvic and retroperitoneal lymphatic pathways. In this review, specific conditions causing nodal involvement of pelvic and retroperitoneal lymphatic pathways in patients with malignant lymphoma that may impact diagnostic and treatment decisions are highlighted.
腹部淋巴途径的淋巴结受累见于多种组织学亚型的恶性淋巴瘤。腹部淋巴途径异常摄取的组织学诊断主要包括B细胞系非霍奇金淋巴瘤和霍奇金淋巴瘤。盆腔和腹膜后淋巴途径的初始受累可由多种潜在的非霍奇金淋巴瘤引起:滤泡性淋巴瘤、弥漫性大B细胞淋巴瘤、黏膜相关淋巴组织(MALT)型边缘区B细胞淋巴瘤和套细胞淋巴瘤。这些临床实体的诊断需要多种成像技术,包括氟-18-氟脱氧葡萄糖((18)FDG)正电子发射断层扫描/计算机断层扫描(PET/CT)、计算机断层扫描、(67)镓闪烁扫描和磁共振成像(MRI)。这些疾病通常缺乏特异性症状,但PET/CT上强烈的(18)FDG积聚可能是疾病活动的标志物。对(18)FDG摄取的存在及特定模式的解读可能无需进行侵入性活检。然而,异常摄取的鉴别往往很难确定,因为(18)FDG在泌尿道或肠道的局灶性积聚可模拟盆腔和腹膜后淋巴途径的淋巴结受累。在本综述中,重点介绍了恶性淋巴瘤患者中导致盆腔和腹膜后淋巴途径淋巴结受累的特定情况,这些情况可能会影响诊断和治疗决策。