@article{oai:soar-ir.repo.nii.ac.jp:00003706,
 author = {Yamazaki,  Masanori and Sato,  Ai and Nishio,  Shin-ichi and Takeda,  Teiji and Miyamoto,  Takahide and Katai,  Miyuki and Hashizume,  Kiyoshi},
 issue = {6},
 journal = {INTERNAL MEDICINE},
 month = {},
 note = {A 33-year-old woman was hospitalized for examination of edematous laryngopharynx. She was acromegalic. A pituitary adenoma with elevated serum levels of growth hormone (GH) and insulin-like growth factor-I (IGF-I) was detected, indicating acromegaly caused by GH-secreting pituitary adenoma. Multiple pigmented nevi were also noted without overt short stature and cubitus valgus. Chromosome analysis revealed that she had contracted Turner syndrome with 47,XXX/45,X/46,XX mosaicism. Transsphenoidal resection of the tumor decreased serum GH and IGF-I levels, but the edema was not improved. Both premature ovarian failure and hypertension appeared after surgery. This case may indicate the important relationships between GH/IGF-I and Turner syndrome., Article, INTERNAL MEDICINE. 48(6):447-453 (2009)},
 pages = {447--453},
 title = {Acromegaly Accompanied by Turner Syndrome with 47,XXX/45,X/46,XX Mosaicism},
 volume = {48},
 year = {2009}
}