18F-FDG PET Imaging Features of Patients With Autoimmune Lymphoproliferative Syndrome. (December 2019)

• Record Type: Journal Article
• Authors: Carrasquillo, Jorge A.; Chen, Clara C.; Price, Susan; Whatley, Millie; Avila, Nilo A.; Pittaluga, Stefania; Jaffe, Elaine S.; Rao, V. Koneti
• Is Part Of: Clinical nuclear medicine. Volume 44:Number 12(2019)
• Publication Date: 2019-12
• Subjects: ALPS -- autoimmune lymphoproliferative disorder -- fluorodeoxyglucose -- lymphoma; Nuclear medicine -- Periodicals; Radioisotope scanning -- Periodicals; Nuclear Medicine -- Periodicals; 616.07575
• DOI: 10.1097/RLU.0000000000002816
• Languages: English
• ISSNs: 0363-9762

Abstract

Abstract : Introduction: Autoimmune lymphoproliferative syndrome (ALPS) is a rare immune dysregulatory condition, usually presenting in childhood with massive lymphadenopathy, splenomegaly, and an increased incidence of lymphoma. Methods to differentiate between benign ALPS adenopathy and lymphoma are needed. To this end, we evaluated the usefulness of FDG PET. Methods: We prospectively evaluated 76 ALPS/ALPS-like patients including F S-7– a ssociated s urface antigen ( FAS ) germline mutation with (n = 4) and without lymphoma (n = 50), FAS -somatic (n = 6), ALPS-unknown (n = 6), and others (n = 10) who underwent FDG PET. Uptakes in 14 nodal sites, liver, and spleen were determined. Results: In 76 ALPS patients, FDG PET showed uptake in multiple nodal sites in all but 1 patient. The highest SUVmax values in FAS mutation without lymphoma, FAS mutation with lymphoma, FAS somatic, ALPS-unknown, and other genetic mutations were a median (range) 9.2 (4.3–25), 16.2 (10.7–37.2), 7.6 (4.6–18.1), 11.5 (4.8–17.2), and 5.5 (0–15.3), respectively. Differences between uptake in the FAS group with and without lymphoma were statistically significant, but overlapped, making discrimination between individuals with/without lymphoma impossible. The spleen:liver uptake ratio was greater than 1 in 82% of patients. Conclusions: While statistically significant differences were observed in FAS mutation ALPS with and without lymphoma, the significant overlap in FDG uptake and visual appearance in many patients prevents discrimination between patients with and without lymphoma. Similar patterns of FDG biodistribution were noted between the various ALPS subgroups.