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PET-CT for Evaluation of Spleen and Liver (18)F-FDG Diffuse Uptake Without Lymph Node Enlargement in Lymphoma

The aim of the study was to compare differences between lymphoma and inflammation as indicated by high diffuse uptake of (18)F-fluorodeoxyglucose ((18)F-FDG) in the spleen, liver, and bone marrow without increased (18)F-FDG uptake in the lymph nodes and without enlarged peripheral lymph nodes. Eight...

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Detalles Bibliográficos
Autores principales: Rao, Liangjun, Wang, Xiaoyan, Zong, Zhen, Chen, Zhifeng, Shi, Xinchong, Yi, Chang, Zhang, Xiangsong, Yang, Zhiyun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4902443/
https://www.ncbi.nlm.nih.gov/pubmed/27196500
http://dx.doi.org/10.1097/MD.0000000000003750
Descripción
Sumario:The aim of the study was to compare differences between lymphoma and inflammation as indicated by high diffuse uptake of (18)F-fluorodeoxyglucose ((18)F-FDG) in the spleen, liver, and bone marrow without increased (18)F-FDG uptake in the lymph nodes and without enlarged peripheral lymph nodes. Eighteen lymphoma patients and 14 inflammation patients were examined with (18)F-FDG positron emission tomography–computer tomography (PET-CT). All patients displayed high diffuse uptake of (18)F-FDG in the spleen, liver, and bone marrow without increased (18)F-FDG uptake in the lymph nodes and without enlarged peripheral lymph nodes. Our analyses compared the maximum standardized uptake values (SUVmax) of (18)F-FDG uptake ratios between the spleen/liver, the spleen/bone marrow, and the liver/bone marrow and further compared spleen sizes between lymphoma and inflammation patients. Using Student t test, no significant differences were found in the SUVmax ratios of spleen/liver and liver/bone marrow between the lymphoma and inflammation patients (t = 0.853, P = 0.401 > 0.05; t = 1.622, P = 0.115 > 0.05). However, the SUVmax ratio of the spleen/bone marrow of the lymphoma patients was significantly different from that of the inflammation patients (t = 2.426, P = 0.021 < 0.05). The spleen size between the lymphoma and inflammation patients was also significantly different (t = 2.911, P = 0.007 < 0.05). As indicated by (18)F-FDG PET-CT, our study demonstrated that lymphoma and inflammation patients displayed a few differences despite both having high diffuse uptake of (18)F-FDG in the spleen, liver, and bone marrow without enlarged peripheral lymph nodes and without increased (18)F-FDG uptake in lymph nodes.