Endocrinology and Metabolism (Mar 2015)

Multiple Myeloma in a Patient with Acromegaly

  • Yu Mi Kang,
  • Jong Han Choi,
  • Min Jung Lee,
  • Ari Ahn,
  • Chan-Jeoung Park,
  • Kiju Chang,
  • Seyoung Seo,
  • Sun In Hong,
  • Min-Seon Kim

DOI
https://doi.org/10.3803/EnM.2015.30.1.110
Journal volume & issue
Vol. 30, no. 1
pp. 110 – 115

Abstract

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Acromegaly is a slowly progressing condition resulting from excess growth hormone (GH), generally caused by a GH-secreting pituitary adenoma. Cancer is the third most common cause of mortality in patients with acromegaly, and insulin-like growth factor 1 (IGF-1) is known to influence tumor formation by increasing cell proliferation and inhibiting apoptosis. Multiple myeloma (MM) is a plasma cell neoplasm, and previous studies have suggested the possible role of IGF-1 in its development of MM. However, no cases of acromegaly accompanied with MM have been reported in Asia to date. We here report the case of a 58-year-old woman with acromegaly accompanied with MM who presented with longstanding acromegalic manifestations resulting from a GH-secreting pituitary adenoma and also exhibited anemia, a reversed albumin/globulin ratio, and plasmacytosis on bone marrow examination. Because IGF-1 has been suggested to play an important role in the development and progression of MM, the patient promptly underwent surgical removal of the pituitary adenoma via a transsphenoidal approach. Since there is currently no consensus on therapeutic guidelines and suggested prognosis for MM with acromegaly, long-term follow-up of such cases is needed.

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