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[Successful control of hyper-cortisolemia due to ACTH-producing thyroid carcinoid by laparoscopic bilateral adrenalectomy : a case report].

Abstract
A 22-year-old man was referred to our hospital because of facial edema and increasing body weight. Under the diagnosis of Cushing syndrome due to an adrenocorticotropic (ACTH)-producing thyroid tumor, thyroidectomy with regional lymph node dissection was performed. Histopathological diagnosis was thyroid carcinoid. In spite of the operation, serum ACTH and cortisol concentrations increased again due to mediastinal lymph node metastasis. His hyper-cortisolemia was resistant to drug therapy. Then, laparoscopic bilateral adrenalectomy was performed. After the operation, hyper-cortisolemia and clinical symptoms markedly improved. An additional chemotherapy is implemented because of new metastasis in the mediastinum lymph nodes.
AuthorsYuta Kojima, Noritaka Kamimura, Hayato Yamamoto, Hiromi Murasawa, Akiko Okamoto, Atsushi Imai, Shingo Hatakeyama, Takahiro Yoneyama, Yasuhiro Hashimoto, Takuya Koie, Chikara Ohyama
JournalHinyokika kiyo. Acta urologica Japonica (Hinyokika Kiyo) Vol. 59 Issue 7 Pg. 419-22 (Jul 2013) ISSN: 0018-1994 [Print] Japan
PMID23945320 (Publication Type: Case Reports, English Abstract, Journal Article)
Chemical References
  • Adrenocorticotropic Hormone
Topics
  • Adrenalectomy
  • Adrenocorticotropic Hormone (biosynthesis)
  • Carcinoid Tumor (complications)
  • Cushing Syndrome (blood, etiology, surgery)
  • Humans
  • Laparoscopy
  • Lymph Node Excision
  • Male
  • Thyroid Neoplasms (complications)
  • Young Adult

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