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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
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pubmed:dateCreated |
1989-5-26
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pubmed:abstractText |
Computer-assisted tomography (CT) with 2 mm axial sections and reconstructions was carried out in 31 children affected by GH deficiency (GHD): 18 with idiopathic complete isolated GHD, 3 with idiopathic partial isolated GHD, 2 with idiopathic panhypopituitarism, 4 with isolated acquired GHD and 4 with acquired panhypopituitarism. Density in the intrasellar area on CT corresponded to that of cerebrospinal fluid in 13/20 cases with idiopathic hypopituitarism and in 2/8 cases with acquired hypopituitarism. The overall incidence of primary empty sella syndrome (PESS) in the GH deficient patients studied was thus over 48%, while in children without endocrine dysfunction, it was only 5/213 (2.4%). It is concluded that PESS is more frequent in childhood than assumed until now and that it is frequently associated with GHD.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Feb
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pubmed:issn |
0018-022X
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
43
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
295-301
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pubmed:dateRevised |
2004-11-17
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pubmed:meshHeading |
pubmed-meshheading:2785096-Adolescent,
pubmed-meshheading:2785096-Adult,
pubmed-meshheading:2785096-Child,
pubmed-meshheading:2785096-Child, Preschool,
pubmed-meshheading:2785096-Craniopharyngioma,
pubmed-meshheading:2785096-Dwarfism, Pituitary,
pubmed-meshheading:2785096-Empty Sella Syndrome,
pubmed-meshheading:2785096-Female,
pubmed-meshheading:2785096-Growth Hormone,
pubmed-meshheading:2785096-Histiocytosis, Langerhans-Cell,
pubmed-meshheading:2785096-Humans,
pubmed-meshheading:2785096-Hypopituitarism,
pubmed-meshheading:2785096-Male,
pubmed-meshheading:2785096-Pituitary Neoplasms
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pubmed:year |
1989
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pubmed:articleTitle |
High frequency of empty sella syndrome in children with growth hormone deficiency.
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pubmed:affiliation |
Clinica Pediatrica, Ospedale Infantile Burlo Garofolo, Università di Trieste, Italy.
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pubmed:publicationType |
Journal Article
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