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A case of duplication of the pituitary gland found by complaint of precocious puberty Sayuri Hakoda 1 1Department of Radiology University of Fukui Hospital Keyword: 重複下垂体 , DPG–plus症候群 , 思春期早発症 pp.403-407
Published Date 2024/5/10
DOI https://doi.org/10.18888/rp.0000002687
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We experienced a case of duplication of the pituitary gland(DPG)in an 8–year–old girl who presented with early onset of puberty. DPG is a rare disorder that has been reported in only about 50 cases. DPG is associated with a high rate of median structural abnormalities such as cleft palate and pharyngeal tumors, which are collectively referred to as DPG–plus syndrome. It can be fatal due to oral malformations, but otherwise endocrinologic manifestations, such as precocious puberty, can be problematic. It is considered necessary to search for a DPG when finding a median structural abnormality.


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