2(F-18)-fluoro-2-deoxy-D-glucose positron emission tomography is a sensitive tool for the detection of occult primary cancer (carcinoma of unknown primary syndrome) with head and neck lymph node manifestation
M. Jungehulsing et al., 2(F-18)-fluoro-2-deoxy-D-glucose positron emission tomography is a sensitive tool for the detection of occult primary cancer (carcinoma of unknown primary syndrome) with head and neck lymph node manifestation, OTO H N SUR, 123(3), 2000, pp. 294-301
BACKGROUND: The neck lymph nodes are a common site of metastases from carci
noma of unknown primary (CUP syndrome). 2(F-18)-fluoro-2-deoxy-D-glucose po
sitron emission tomography (18-FDG-PET) has been shown to be a sensitive to
ol for detecting primary malignant lesions as well as metastatic spread. We
have prospectively investigated the sensitivity of 18-FDG-PET in detecting
occult primary carcinomas with manifestation in the head and neck lymph no
des.
METHODS: From May 1994 to July 1998, in 723 patients a cancer of the head a
nd neck was diagnosed at the University of Cologne ENT outpatient clinic. T
he routinely performed staging procedures were chest radiography; full bloo
d count; cervical and liver ultrasound; endoscopy of the nasopharynx, oroph
arynx, hypopharynx, larynx, and esophagus; and laboratory analyses. After t
he staging workup, in 27 of 723 patients (3.7%) CUP syndrome had to be pres
umed because the primary cancer could not be detected. In these patients 18
-FDG-PET was performed, and images were reconstructed with a transmission-e
mission fusion technique.
RESULTS: In 7 of 27 patients (26%) 18-FDG-PET revealed an unknown primary:
in 2 a bronchial carcinoma, in 2 a nasopharyngeal carcinoma, in 1 a squamou
s cell carcinoma of the parotid gland, in 1 a squamous cell carcinoma of th
e hypopharynx, and in 1 a carcinoma of the tonsil. In 4 of 7 patients the o
ccult primary tumor was removed surgically. In 8 of 27 patients therapeutic
strategy was changed as a result of the 18-FDG-PET findings.
CONCLUSION: 18-FDG-PET should be performed in all patients with CUP syndrom
e after conventional diagnostic workup fails to identify the primary.