Diagnostic utility of <SUP>68</SUP>Ga- citrate and <SUP>18</SUP>F-FDG PET/CT in sarcoidosis patients


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Tetikkurt C., Yanardag H., Sayman B. H., Bilir M., Tetikkurt S., Bilgic S., ...More

MONALDI ARCHIVES FOR CHEST DISEASE, vol.90, no.4, pp.729-737, 2020 (ESCI) identifier identifier identifier

  • Publication Type: Article / Article
  • Volume: 90 Issue: 4
  • Publication Date: 2020
  • Doi Number: 10.4081/monaldi.2020.1509
  • Journal Name: MONALDI ARCHIVES FOR CHEST DISEASE
  • Journal Indexes: Emerging Sources Citation Index (ESCI), Scopus, EMBASE, MEDLINE, Directory of Open Access Journals
  • Page Numbers: pp.729-737
  • Bursa Uludag University Affiliated: No

Abstract

Sarcoidosis is a chronic granulomatous disease of unknown etiology. The disease most commonly involves the lungs and the mediastinal lymph nodes while extrapulmonary organs such as the skin, eye, liver or spleen may also be comprised. Many imaging modalities have been used for the clinical evaluation of sarcoidosis patients, but all have been found to have certain drawbacks for a reliable diagnostic assessment due to the equivocal diagnostic results. This study was designed to determine the clinical trenchancy of simultaneous Ga-68-citrate PET/CT [Positron emission tomography with Ga-68-citrate (Ga-68-citrate PET/CT)] and F-18-FDG PET/CT [Positron emission tomography with 2-deoxy-2-[fluorine-18] fluoro-D-glucose (F-18-FDG PET/CT)] imaging in sarcoidosis patients. The main goal was to evaluate sarcoidosis patients with respect to diagnosis, disease activity and organ involvement. A total of eight sarcoidosis patients with a comorbid disease suspicion were included in the study. Conventional clinical parameters used for the diagnosis and the activity of sarcoidosis including clinical, laboratory and computed tomography (CT) manifestations were compared with the Ga-68-citrate PET/CT findings. Concurrent F-18-FDG PET/CT was performed to verify the granulomatous inflammation of sarcoidosis and to determine coexisting malignant or other inflammatory diseases. Our study results revealed that Ga-68-citrate PET/CT imaging appears to be highly useful for the diagnosis, activity assessment and extrapulmonary organ involvement in sarcoidosis. Another crucial finding was the detection of extrapulmonary organ disease that are exceptionally involved, almost inaccessible by biopsy and that could not be otherwise displayed by other conventional imaging modalities. The third hallmark was the identification of a clinically asymptomatic and occult malignancy accompanying sarcoidosis that would not be detected in any way if synchronous F-18-FDG PET/CT had not been performed. Simultaneous application of Ga-68-citrate and (18)FFDG PET/CT may provide extremely useful data for the clinical evaluation of sarcoidosis patients in terms of the primary disease diagnosis, activity state, extrapulmonary organ involvement unachievable for biopsy and revealing occult malignant disorders that may coexist with sarcoidosis.