Distinctive FDG and FES accumulation pattern of two tamoxifen-treated patients with endometrial hyperplasia
Distinctive FDG and FES accumulation pattern of two tamoxifen-treated patients with endometrial hyperplasia
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DOI:
10.1007/s12149-007-0075-2
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发表时间:
2008
影响因子:
2.6
通讯作者:
T. Tsujikawa;H. Okazawa;Y. Yoshida;T. Mori;Masato Kobayashi;T. Tsuchida;Y. Fujibayashi
中科院分区:
文献类型:
--
作者:
T. Tsujikawa;H. Okazawa;Y. Yoshida;T. Mori;Masato Kobayashi;T. Tsuchida;Y. Fujibayashi
16α-[18F]Fluoro-17β-estradiol (FES) is an estrogen receptor (ER) ligand used for the detection of ER-positive malignant tumors such as breast cancer. We recently reported the feasibility of combined FES-and 2-[18F]fluoro-2-deoxy-D-glucose (FDG)-positron emission tomography (PET) scans for the differential diagnosis of endometrial tumors. ER expression measured by FES-PET was preserved in endometrial hyperplasia, whereas ERs were assumed to be reduced in endometrial carcinoma with accelerated glucose metabolism measured by FDG-PET. We report two postmenopausal patients under suspicion of endometrial carcinoma on the basis of cytology and/or magnetic resonance imaging (MRI), who were on tamoxifen treatment since undergoing surgery for breast cancer. Pelvic MRI suggested endometrial carcinomas, whereas FDG-and FES-PET showed no abnormal tracer accumulation. A postoperative histopathologic examination revealed that the lesions were endometrial hyperplasias with no malignant findings. FES-PET enables us to evaluate the ERα expression of endometrium noninvasively, whereas the evaluation of ER expression using FES-PET requires careful attention regarding the influence of hormonal therapy because tamoxifen greatly affects FES accumulation of even endometrial hyperplasia, which should be an FES-avid lesion.