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(18)F-FDG PET/CT imaging findings in anaplastic large cell lymphoma, a rare subtype of lymphoma

OBJECTIVE: To investigate the (18)F-FDG PET/CT imaging manifestations for anaplastic large cell lymphoma (ALCL), a rare subtype of T/NK cell lymphoma. METHODS: Fifty patients with ALCL, including 32 anaplastic lymphoma kinase (ALK)-positive patients and 18 ALK-negative patients, were enrolled. The p...

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Detalles Bibliográficos
Autores principales: Jiang, Yanping, Wang, Lijuan, Zhou, Wenlan, Gu, Jiamei, Tian, Ying, Dong, Ye, Fu, Lilan, Wu, Hu-bing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6954597/
https://www.ncbi.nlm.nih.gov/pubmed/31924270
http://dx.doi.org/10.1186/s40644-019-0278-5
Descripción
Sumario:OBJECTIVE: To investigate the (18)F-FDG PET/CT imaging manifestations for anaplastic large cell lymphoma (ALCL), a rare subtype of T/NK cell lymphoma. METHODS: Fifty patients with ALCL, including 32 anaplastic lymphoma kinase (ALK)-positive patients and 18 ALK-negative patients, were enrolled. The positive detection, maximal standardized uptake value (SUV(max)), and distribution of nodal and extranodal involvement were recorded and analysed. Fifty patients with diffuse large B cell lymphoma (DLBCL) were collected as a control group. RESULTS: ALCL lesions were demonstrated to be (18)F-FDG-avid tumours with a mean SUVmax of 19.4 ± 12.6. Most (76%) ALCL patients presented with stage III-IV disease, and nodal and extranodal involvement occurred in 74.0 and 72.0% of the patients, respectively. ALCL and DLBCL showed many similarities in tumour stage, (18)F-FDG uptake and tumour involvement (P > 0.05), although the preferred extranodal organs of involvement (bone and the gastrointestinal tract, respectively) were different (P < 0.05). Compared to ALK-negative lesions, a higher uptake of (18)F-FDG was found in the ALK-positive lesions (SUVmax: 22.1 ± 14.3 vs. 15.1 ± 6.6, t = 2.354, P = 0.023). ALK-positive ALCL was more likely to involve the lymph nodes than ALK-negative ALCL (84.3% vs. 55.5%, χ(2) = 4.973, P = 0.043), while ALK-negative ALCL was more prone to involve the extranodal organs compared to ALK-positive ALCL (88.9% vs. 62.5%, χ(2) = 3.979, P = 0.046). CONCLUSION: The present study demonstrated that ALCL is a systemic (18)F-FDG-avid lymphoma with many imaging manifestations similar to DLBCL on PET/CT. The present study also showed that ALK expression actually influenced tumour (18)F-FDG uptake and lesion distribution. These findings may be useful to improve the understanding of the biological characteristics of ALCL.