WordNet

present at birth but not necessarily hereditary; acquired during fetal development (同)inborn, innate
of or derived from the cortex of the adrenal glands
abnormal increase in number of cells

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Steroid profiling by gas chromatography-mass spectrometry and high performance liquid chromatography-mass spectrometry for adrenal diseases.

McDonald JG, Matthew S, Auchus RJ.SourceDepartment of Molecular Genetics, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Hormones & cancer.Horm Cancer.2011 Dec;2(6):324-32.
The ability to measure steroid hormone concentrations in blood and urine specimens is central to the diagnosis and proper treatment of adrenal diseases. The traditional approach has been to assay each steroid hormone, precursor, or metabolite using individual aliquots of serum, each with a separate
PMID 22170384

Primary bimorphic adrenocortical disease: cause of hypercortisolism in McCune-Albright syndrome.

Carney JA, Young WF, Stratakis CA.SourceDepartment of Laboratory Medicine and Pathology, Division of Endocrinology, Diabetes, Nutrition and Metabolism, Mayo Clinic, 200 First Street SW, Rochester, MN 55905, USA. carney.aidan@mayo.edu
The American journal of surgical pathology.Am J Surg Pathol.2011 Sep;35(9):1311-26.
McCune-Albright syndrome (polyostotic fibrous dysplasia, café-au-lait skin spots, and precocious puberty) is a genetically mosaic disorder with populations of mutant and normal cells in affected organs. Cushing syndrome, a rare feature of the condition, usually affects infants and is the result of
PMID 21836496

A Male Case of Nonclassical 21-hydroxylase Deficiency First Manifested in His Sixties with Adrenocortical Incidentaloma

NIGAWARA TAKESHI,KAGEYAMA KAZUNORI,SAKIHARA SATORU,TAKAYASU SHINOBU,KAWAHARA MASAYUKI,IMAI ATSUSHI,OHYAMA CHIKARA,USUI TAKESHI,SASANO HIRONOBU,SUDA TOSHIHIRO
Endocrine journal 55(2), 291-297, 2008-04-01
NAID 10021265503

A Male Case of Nonclassical 21-hydroxylase Deficiency First Manifested in His Sixties with Adrenocortical Incidentaloma

NIGAWARA Takeshi,KAGEYAMA Kazunori,SAKIHARA Satoru,TAKAYASU Shinobu,KAWAHARA Masayuki,IMAI Atsushi,OHYAMA Chikara,USUI Takeshi,SASANO Hironobu,SUDA Toshihiro
Endocrine Journal 55(2), 291-297, 2008
… Nonclassical form of 21-hydroxylase deficiency (NC 21OHD) as a frequent variant on the milder end of the disease spectrum has been widely acknowledged, but its potential contribution to adrenocortical tumorigenesis has not been fully elucidated. … We report a 66-year old male case of bilateral adrenocortical incidentaloma, associated with partial 21OHD without any episodes of hypoadrenocorticism in his past history. …
NAID 130004443391

Evaluation of Hypothalamo-Pituitary-Adrenocortical Function in Children by Human Corticotropin-Releasing Hormone (MCI-028) Test.

TANAKA TOSHIAKI,HIBI ITSURO,SHIMIZU NAOKATA,IMURA HIROO,TANAKA KOSHI,FUKATA JUNICHI,FUJIEDA KENJI,ICHIMURA TOHJU,KURIBAYASHI TAKEO,ITO KATSUMI,SUWA SEIZO,TACHIBANA KATSUHIKO,KATO KIYOHIKO,OHTA MASANORI,YANAIHARA NOBORU
Endocrine Journal 40(5), 581-589, 1993
… A dose of 1.5μg/kg of MCI-028, human corticotropin-releasing hormone (hCRH), was administered intravenously to 38 children with non-endocrine short stature with normal function in the hypothalamo-pituitary-adrenocortical axis and to 71 children with a disorder in the same axis. …
NAID 130003549380