Concurrent papillary thyroid cancer with pituitary ACTH-secreting tumor

  • Sheng Fong Kuo
  • , Jeng Yeou Chen
  • , Wen Yu Chuang
  • , Shih Ming Jung
  • , Fu Chen Chang
  • , Jen Der Lin*
  • *Corresponding author for this work

Research output: Contribution to journalJournal Article peer-review

1 Scopus citations

Abstract

Concomitant thyroid cancer with pituitary tumor is uncommon. This study reports a case of advanced papillary thyroid carcinoma with pituitary adrenocorticotropic hormone (ACTH)-secreting tumor. A 58-year-old male patient had thyroid cancer in 1991 and presented with headache caused by pituitary tumor with apoplexy in 1993. Due to hypopituitarism, the patient underwent radioactive iodide (131I) for detection and treatment of metastatic thyroid cancer after the use of recombinant human thyroid-stimulating hormone (rhTSH) in 2000. During follow-up for thyroid cancer, 201thallium scan proved to be an effective tool for detecting metastatic thyroid cancer in the patient without pituitary TSH reserve. Pituitary ACTH-secreting tumor was confirmed in 2001 based on the high serum ACTH level and positive immunohistochemical stain for ACTH. The patient had no Cushingoid features. Moreover, serum ACTH levels were 337 and 232 pg/mL with normal serum cortisol and urine-free cortisol. Although the patient underwent three operations and a total of 370 mCi 131I therapy for recurrent thyroid cancer, the cancer continued to progress. Finally, the patient died of pneumonia with septic shock 12 years after the diagnosis of thyroid cancer.

Original languageEnglish
Pages (from-to)330-335
Number of pages6
JournalJournal of the Formosan Medical Association
Volume106
Issue number4
DOIs
StatePublished - 04 2007

Keywords

  • Papillary thyroid carcinoma
  • Pituitary ACTH-secreting tumor
  • Preclinical Cushing's disease
  • Silent corticotroph adenoma
  • hallium scan

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