Boninsegna Enrico, Zamboni Giulia A, Facchinelli Davide, Triantopoulou Charikleia, Gourtsoyianni Sofia, Ambrosetti Maria Chiara, Veneri Dino, Ambrosetti Achille, Pozzi Mucelli Roberto
Department of Radiology, Policlinico G. B. Rossi, University of Verona, Verona, Italy.
Department of Medicine, Section of Hematology, University of Verona, Verona, Italy.
Insights Imaging. 2018 Feb;9(1):17-24. doi: 10.1007/s13244-017-0585-y. Epub 2018 Jan 15.
To describe CT characteristics of primary pancreatic lymphoma (PPL), a rare disease with features in common with adenocarcinoma.
Fourteen patients were enrolled. CT: unenhanced scan, contrast-enhanced pancreatic and venous phases. Image analysis: tumour location; peri-pancreatic vessel encasement; necrosis; enlarged lymph nodes; fat stranding; enlarged bile duct and pancreatic duct; neoplasm longest dimension, volume and density.
Histopathological diagnoses: follicular non-Hodgkin lymphoma (5/14), diffuse large B-cell lymphoma (6/14) and high-grade B-cell lymphoma not otherwise specified (3/14). Six of 14 PPLs were located in the pancreatic head and 7/14 in the body-tail; 1/14 involved the whole gland. In 5/14 cases the superior mesenteric artery and vein were encased; splenic vein and artery encasement was depicted in 2 PPLs. Necrosis was present in 2/14. Enlarged retroperitoneal lymph nodes were found in 11 cases and fat stranding in all patients. The bile duct was dilated in six cases and the pancreatic duct in five. Mean neoplasm longest diameter and volume were 8.05 cm and 210.8 cm. Mean tumour attenuation values were 39.1 HU at baseline, 60.6 HU in the pancreatic phase and 71.4 HU in the venous phase.
PPL presents as a large mass lesion with delayed homogeneous enhancement; peri-pancreatic fat stranding and vessel encasement are present, without vascular infiltration. Pancreatic duct dilatation is rare.
• Primary pancreatic lymphoma (PPL) is a rare haematological disease • PPL presents imaging features in common with pancreatic carcinoma but also some distinctive findings • The majority of PPLs are large lesions with delayed homogeneous enhancement • Peri-pancreatic fat stranding and vessel encasement are common in PPL • Vascular infiltration and pancreatic duct dilatation are rare in PPL.
描述原发性胰腺淋巴瘤(PPL)的CT特征,这是一种与腺癌有共同特征的罕见疾病。
纳入14例患者。CT检查:平扫、胰腺期及静脉期增强扫描。图像分析:肿瘤位置;胰腺周围血管包绕情况;坏死;肿大淋巴结;脂肪间隙模糊;胆管及胰管扩张;肿瘤最长径、体积及密度。
组织病理学诊断:滤泡性非霍奇金淋巴瘤(5/14)、弥漫性大B细胞淋巴瘤(6/14)及未另行特指的高级别B细胞淋巴瘤(3/14)。14例PPL中,6例位于胰头,7例位于胰体尾部,1例累及全胰腺。14例中有5例肠系膜上动静脉被包绕,2例显示脾动静脉被包绕。14例中有2例存在坏死。11例发现腹膜后淋巴结肿大,所有患者均有脂肪间隙模糊。6例胆管扩张,5例胰管扩张。肿瘤平均最长径和体积分别为8.05 cm和210.8 cm³。肿瘤平均衰减值在平扫时为39.1 HU,胰腺期为60.6 HU,静脉期为71.4 HU。
PPL表现为较大的肿块性病变,强化延迟且均匀;存在胰腺周围脂肪间隙模糊及血管包绕,无血管浸润。胰管扩张少见。
•原发性胰腺淋巴瘤(PPL)是一种罕见的血液系统疾病 •PPL呈现出与胰腺癌共同的影像学特征,但也有一些独特表现 •大多数PPL为较大病变,强化延迟且均匀 •胰腺周围脂肪间隙模糊及血管包绕在PPL中常见 •PPL中血管浸润及胰管扩张少见