ID | 111531 |
Title Alternative | Familial pituitary tumors
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Author |
Yoshimoto, Katsuhiko
The University of Tokushima
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Saito, Shiro
The University of Tokushima
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Keywords | MEN 1
Familial pituitary adenomas
Acromegaly
Prolactinoma
Allelic deletion
11q13
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Content Type |
Journal Article
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Description | Familial pituitary tumors are relatively rare. Most commonly, they occur as a part of multiple endocrine neoplasia type 1 (MEN 1). However, familial pituitary adenomas unrelated MEN 1 (familial pituitary adenomas) are extremely rare. In review of MEN 1 in Japan, 60% of the patients with MEN 1 had pituitary tumors. Only 45 cases of familial pituitary adenomas have been reported from 20 families. In our review of familial pituitary adenomas, 30 (67%) of 45 reported cases are acromegaly or gigantism. This incidence is much higher than 28% in MEN 1 patients with pituitary tumors. Allelic deletions at 11q13 were identified in MEN 1 associated pituitary adenomas and familial pituitary adenomas in two gigantism brothers.
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Journal Title |
Japanese journal of clinical medicine
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ISSN | 00471852
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NCID | AN00198641
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Publisher | 日本臨牀社
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Volume | 53
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Issue | 11
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Start Page | 2691
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End Page | 2696
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Published Date | 1995-11
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EDB ID | |
FullText File | |
language |
jpn
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TextVersion |
Publisher
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departments |
Oral Sciences
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