rdf:type |
|
lifeskim:mentions |
|
pubmed:issue |
43
|
pubmed:dateCreated |
1996-12-10
|
pubmed:abstractText |
A 29-year-old woman was found to have arterial hypertension (175/115 mm Hg). The 24-hour profile showed no diurnal cortisol variations with normal concentrations and 24-hour urinary cortisol was normal. 14 months later there was definite hypercortisolism with discrete Cushing signs and no amenorrhoea. She also had signs of depression.
|
pubmed:language |
ger
|
pubmed:journal |
|
pubmed:citationSubset |
IM
|
pubmed:chemical |
|
pubmed:status |
MEDLINE
|
pubmed:month |
Oct
|
pubmed:issn |
0012-0472
|
pubmed:author |
|
pubmed:issnType |
Print
|
pubmed:day |
25
|
pubmed:volume |
121
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
1321-4
|
pubmed:dateRevised |
2006-11-15
|
pubmed:meshHeading |
pubmed-meshheading:8964212-Adrenal Cortex,
pubmed-meshheading:8964212-Adrenal Cortex Diseases,
pubmed-meshheading:8964212-Adrenalectomy,
pubmed-meshheading:8964212-Adult,
pubmed-meshheading:8964212-Blood Pressure,
pubmed-meshheading:8964212-Cushing Syndrome,
pubmed-meshheading:8964212-Diagnosis, Differential,
pubmed-meshheading:8964212-Female,
pubmed-meshheading:8964212-Humans,
pubmed-meshheading:8964212-Hydrocortisone,
pubmed-meshheading:8964212-Magnetic Resonance Imaging,
pubmed-meshheading:8964212-Melanoma,
pubmed-meshheading:8964212-Shoulder,
pubmed-meshheading:8964212-Skin Neoplasms
|
pubmed:year |
1996
|
pubmed:articleTitle |
[Primary pigmented nodular adrenocortical dysplasia. A rare cause of Cushing's syndrome].
|
pubmed:affiliation |
Medizinische Universitätsklinik, Abteilung IV (Nephrologie), Institut der Universität, Freiburg.
|
pubmed:publicationType |
Journal Article,
English Abstract,
Case Reports
|