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Congruence of Ga-68 Dotanoc positron emission tomography-computed tomography and metaiodobenzylguanidine scan in a patient of metastatic medullary thyroid carcinoma
Address for correspondence: Dr. Arvind Krishnamurthy, Department of Surgical Oncology, Cancer Institute (WIA), 36, Sardar Patel Road, Adyar, Chennai - 600 020, Tamil Nadu, India. E-mail: drarvindkrishnamurthy@yahoo.co.in
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Sir,
A 45-year-old man with no co-morbid conditions, presented to us with multiple right sided neck nodes and mass abdomen of 6 months duration. He had undergone a total thyroidectomy for medullary carcinoma thyroid (MTC) elsewhere in 2004. Clinical examination revealed a vague nodularity along the thyroidectomy scar and multiple right sided neck nodes along levels II, III and IV, the largest level III node measuring 3 cm × 2 cm. He also has a non-tender, nodular hepatomegaly, which was palpable 6 cm below the right costal margin. The baseline serum levels of calcitonin and carcinoembryonic antigen (CEA) were elevated at 4745 pg/ml and 7050 ng/ml, respectively. His 24 h urinary metanephrine levels were within normal limits (1.3 mg/day). Aspiration cytology from the right level III node, ultrasound guided biopsy from the liver on correlation with the histopathology slides confirmed a diagnosis of metastatic MTC.
A Ga-68 Dotanoc somatostatin analog positron emission tomography-computed tomograph (PET-CT) scan and a I-131 metaiodobenzylguanidine (MIBG) scan were done as a part of the metastatic evaluation. Ga-68 accumulation was seen in the following regions; residual thyroid gland, multiple cervical and superior mediastinal lymph nodes, multiple lesions in the liver, largest 8.2 cm × 8 cm in segment VIII and right iliac bone measuring 2.2 cm × 1.7 cm [Figure 1].

The MIBG scan showed metabolically active uptakes in bilateral cervical and superior mediastinal lymph nodes, the liver and the right side of pelvis anatomically corresponding to the uptakes seen in the Ga-68 Dotanoc PET-CT [Figure 2]. The MIBG scan and the Ga-68 Dotanoc PET-CT scan [Figure 3] showed a near total congruence. This is supposedly a very rare phenomenon as the uptakes in the MIBG scan and the traditional somatostatin scintigraphic scans are reported to be mutually independent of one another.[1–3] The patient was not keen on considering experimental therapies with targeted agents. He is presently asymptomatic and is on follow up for more than 2 years with stable disease after two ablations (100 and 65 mCi) with I-131 MIBG therapy. The levels of serum calcitonin decreased to 1038 and 758 pg/ml after the first and second ablations, respectively.


MTC which accounts for 4% of thyroid carcinomas originates from neuroendocrine parafollicular C cells and is known to secrete calcitonin and CEA. Conventional radiological modalities such as ultrasound, computerized tomography, and magnetic resonance imaging are used for detecting recurrences following total thyroidectomy in MTC. However, metastatic MTC is known to escape detection by the above modalities, despite the presence of persistently elevated serum calcitonin levels.
Numerous radio-pharmaceuticals are currently being used for detecting recurrences and distant metastases from MTC such as I-131 MIBG, technetium (Tc)-99m dimercaptosuccinyl acid and Tc-99m methoxyisobutylisonitril, fluorodeoxyglycose (FDG) PET-CT and 3,4-dihydroxy-6-F-18 fluoro-L-phenylalanin (F-18-DOPA PET-CT) with varying sensitivities and specificities. Somatostatin receptors are present in MTCs; however, their distribution is heterogeneous making traditional somatostatin receptor scintigraphy of limited usefulness for detection of metastatic MTC. However, the Ga-68 somatostatin analogue Dotanoc PET-CT has been reported to be useful in the detection of neuroendocrine tumors; its use in detecting recurrent/metastatic MTC patients is promising.[4] Our case also shows Ga-68 Dotanoc PET-CT to be a useful complementary imaging modality in detection of recurrent/metastatic disease in patients with MTC, additionally its congruence with the MIBG scan uptakes needs to be further studied.
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