Symptomatic Rathke's Cleft Cyst Coexisting with Central Diabetes Insipidus and Hypophysitis: Case Report.
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Accession number;99A0439798
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| Title;Symptomatic Rathke's Cleft Cyst Coexisting with Central Diabetes Insipidus and Hypophysitis: Case Report. |
| Author;
HAMA S
(Hiroshima Univ. School Of Medicine, Hiroshima, Jpn)
ARITA K
(Hiroshima Univ. School Of Medicine, Hiroshima, Jpn)
TOMINAGA A
(Hiroshima Univ. School Of Medicine, Hiroshima, Jpn)
YOSHIKAWA M
(Hiroshima Univ. School Of Medicine, Hiroshima, Jpn)
EGUCHI K
(Hiroshima Univ. School Of Medicine, Hiroshima, Jpn)
SUMIDA M
(Hiroshima Univ. School Of Medicine, Hiroshima, Jpn)
INAI K
(Hiroshima Univ. School Of Medicine, Hiroshima, Jpn)
NISHISAKA T
(Hiroshima Univ. School Of Medicine, Hiroshima, Jpn)
KURISU K
(Hiroshima Univ. School Of Medicine, Hiroshima, Jpn)
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Journal Title;Endocr J
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Journal Code:F0625A
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ISSN:0918-8959
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VOL.46;NO.1;PAGE.187-192(1999)
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| Figure&Table&Reference;FIG.3, TBL.2, REF.20 |
| Pub. Country;Japan |
| Language;English |
| Abstract;We describe a 48-year-old female with acute of central diabetes insipidus followed by mild anterior pituitary dysfunction. Magnetic resonance imaging(MRI) revealed enlargement of the hypophysis-infundibulum accompanied by a cystic component. She underwent a transsphenoidal exploration of the sella turcica. Histological examination showed foreign body type xanthogranulomatous inflammation in the neurohypophysis which might have been caused by rupture of a Rathke's cleft cyst. The MRI abnormalities and anterior pituitary dysfunction improved after a short course of corticosteroid administration, but the diabetes insipidus persisted. The histological findings in this case indicated the site of RCC rupture and the direction of the progression of RCC induced neurohypophysitis and adenohypophysitis. (author abst.) |
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