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. Author manuscript; available in PMC: 2014 Aug 1.
Published in final edited form as: Clin Endocrinol (Oxf). 2013 May 6;79(2):170–177. doi: 10.1111/cen.12126

Table 1.

Lesion-based sensitivity of 18F-FDOPA PET across different tumour locations in relation to genotype.

A Parasympathetic (HNPGL and parasympathetic thoracic) B Adrenal C Sympathetic Extra-adrenal (Abdominal and sympathetic thoracic) All locations
Number of PGL/PHEO 109 [57/52] 49 [16/33] 37 [17/20] 195 [90/105]
Per-lesion sensitivity 107 (98.2%) [96.5%/100%] 46 (93.9%) [93.8%/93.9%] 26 (70.3%) [47.1%/90%] 179 (91.8%) [86.7%/96.2%]
Genotype of 18F-FDOPA negative tumours 1 SDHD, 1 sporadic 3 SDHD 7 SDHD
4 SDHB
1 sporadic [1/0]
11 SDHD [8/3]
4 SDHB [3/1]

Results of the two series are detailed ([Timone/NIH]) just below the pooled results.

*

The SDHD-related vagal PGL was millimetric and located just below another highly avid PGL of the vagus nerve.

**

The sporadic carotid body tumour was mainly fibrotic, with a minimal residual volume of neuroendocrine tissue.

18F-FDOPA PET was more sensitive in parasympathetic PGL than in sympathetic PGL. A vs B vs C: P<0.001, A vs B: P=0.173, A vs C: P<0.001, B vs C: P=0.006, A vs B+C: P<0.001 (Fisher’s exact test).