Cholestatic syndrome as initial manifestation of pancreatic metastasis of papillary thyroid carcinoma: case report and review
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Arch Endocrinol Metab.
Abstract
Most papillary thyroid carcinomas (PTC) harbor excellent prognosis. Although rare, distant metastases
normally occur in lungs and/or bones. Here we describe a rare case of pancreatic metastasis
presenting with rapid onset cholestatic syndrome. A literature review was also performed. A 73-year old man with a high risk PTC was submitted to total thyroidectomy (TT) followed by radioiodine
therapy. After initial therapy, he persisted with progressive rising serum thyroglobulin levels but with
no evidence of structural disease. Recently, the patient presented with a rapid onset and progressive
cholestatic syndrome. A 4 cm lesion in pancreas was identified, with echoendoscopy fine-needle
aspiration biopsy (FNAB) confirming a pancreatic metastasis from PTC. The patient was submitted
to a successful pancreaticoduodenectomy. Pancreatic metastases of PTC are rare and few long-term
follow-up data are available to guide management. Fourteen cases were former reported, mean age
was 65.7 years-old with mean time between PTC and pancreatic metastasis diagnosis of 7.9 years.
Nine of them had another distant metastasis, nine were diagnosed by FNAB and just two received
sorafenib.
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p. 1-6.: tab. p&b,
Citation
TRAMONTIN, Mariana Yoshii et al. Cholestatic syndrome as initial manifestation of pancreatic metastasis of papillary thyroid carcinoma: case report and review. Arch Endocrinol Metab., v. 64, n. 2, p. 1-6, 2020.