A Case of a TSH-secreting Pituitary Adenoma Associated with Evans' Syndrome.

نویسندگان

  • Atsushi Yasuda
  • Toshiro Seki
  • Masayuki Oki
  • Atsushi Takagi
  • Chie Inomoto
  • Naoya Nakamura
  • Hideki Atsumi
  • Tanefumi Baba
  • Mitsunori Matsumae
  • Noriko Sasaki
  • Yasuo Suzuki
  • Masafumi Fukagawa
چکیده

We present a case of a TSH-secreting pituitary adenoma (TSHoma) associated with Evans' syndrome. A 30-year-old woman was referred to our hospital due to purpura and ecchymoses on her limb and body and epistaxis. Evans' syndrome was diagnosed based on idiopathic thrombocytopenic purpura and autoimmune hemolytic anemia. She had a history of malocclusion and thyroid gland enlargement 4 years prior to admission. Endocrinological tests and magnetic resonance imaging also revealed that this patient had hyperthyroidism due to the TSHoma and that this adenoma concomitantly secreted GH. Recently, several cases of Evans' syndrome were associated with hyperthyroidism caused by autoimmune thyroid disease, such as Graves' disease, suggesting that these 2 conditions may have a common immunological basis. To the best of our knowledge, there is no case report of Evans' syndrome associated with hyperthyroidism due to TSHoma. Our report suggests that the excess of thyroid hormone itself promotes autoimmunity in Evans' syndrome. Thus, early treatment for hyperthyroidism is necessary in TSHomas because of the possibility that thyroid hormone normalization may prevent the development of Evans' syndrome.

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عنوان ژورنال:
  • The Tokai journal of experimental and clinical medicine

دوره 40 2  شماره 

صفحات  -

تاریخ انتشار 2015