TY - JOUR
T1 - 18F-FDG PET/CT in the management of patients with post-transplant lymphoproliferative disorder
AU - Takehana, Christopher S.
AU - Twist, Clare J.
AU - Mosci, Camila
AU - Quon, Andrew
AU - Mittra, Erik
AU - Iagaru, Andrei
PY - 2014/3
Y1 - 2014/3
N2 - Objectives: Post-transplant lymphoproliferative disorder (PTLD) is a rare but serious complication in transplant patients. Although fluorine-18 2-fluoro-2-deoxyglucose PET and computed tomography (18F-FDG PET/CT) has been used for the evaluation and management of patients with PTLD, its utility has yet to be documented. We were therefore prompted to review our experience with 18F-FDG PET/CT in PTLD. Materials and methods: We retrospectively reviewed the records of consecutive patients who had undergone 18F-FDG PET/CT for evaluation of PTLD from January 2004 to June 2012 at our institution. 18F-FDG PET/CT scans were compared with other imaging modalities performed concurrently. A chart review of pertinent clinical information was also conducted. Results: A total of 30 patients were identified (14 female and 16 male; 1.7-76.7 years of age, average: 23.8 years). Twenty-seven participants had biopsy-proven PTLD and another three had been treated for PTLD because of high clinical suspicion of disease and positive 18F-FDG PET/CT findings in the absence of histological diagnosis. Eighty-three percent of these PTLD patients had extranodal involvement. In 57% of the cases, 18F-FDG PET/CT detected occult lesions not identified on other imaging modalities or suggested PTLD in equivocal lesions. The more aggressive PTLD histological subtypes demonstrated higher SUVmax compared with the less aggressive subtypes. Conclusion: 18F-FDG PET/CT is beneficial in the diagnostic evaluation of patients with PTLD. 18F-FDG PET/CT has the ability to detect occult lesions not identified on other imaging modalities, particularly extranodal lesions. In addition, 18F-FDG PET/CT may predict the PTLD subtype, as the lesions with higher pathologic grade presented with significantly higher SUV max compared with the less aggressive forms.
AB - Objectives: Post-transplant lymphoproliferative disorder (PTLD) is a rare but serious complication in transplant patients. Although fluorine-18 2-fluoro-2-deoxyglucose PET and computed tomography (18F-FDG PET/CT) has been used for the evaluation and management of patients with PTLD, its utility has yet to be documented. We were therefore prompted to review our experience with 18F-FDG PET/CT in PTLD. Materials and methods: We retrospectively reviewed the records of consecutive patients who had undergone 18F-FDG PET/CT for evaluation of PTLD from January 2004 to June 2012 at our institution. 18F-FDG PET/CT scans were compared with other imaging modalities performed concurrently. A chart review of pertinent clinical information was also conducted. Results: A total of 30 patients were identified (14 female and 16 male; 1.7-76.7 years of age, average: 23.8 years). Twenty-seven participants had biopsy-proven PTLD and another three had been treated for PTLD because of high clinical suspicion of disease and positive 18F-FDG PET/CT findings in the absence of histological diagnosis. Eighty-three percent of these PTLD patients had extranodal involvement. In 57% of the cases, 18F-FDG PET/CT detected occult lesions not identified on other imaging modalities or suggested PTLD in equivocal lesions. The more aggressive PTLD histological subtypes demonstrated higher SUVmax compared with the less aggressive subtypes. Conclusion: 18F-FDG PET/CT is beneficial in the diagnostic evaluation of patients with PTLD. 18F-FDG PET/CT has the ability to detect occult lesions not identified on other imaging modalities, particularly extranodal lesions. In addition, 18F-FDG PET/CT may predict the PTLD subtype, as the lesions with higher pathologic grade presented with significantly higher SUV max compared with the less aggressive forms.
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U2 - 10.1097/MNM.0000000000000050
DO - 10.1097/MNM.0000000000000050
M3 - Article
C2 - 24296883
AN - SCOPUS:84893759583
SN - 0143-3636
VL - 35
SP - 276
EP - 281
JO - Nuclear Medicine Communications
JF - Nuclear Medicine Communications
IS - 3
ER -