https://scholars.lib.ntu.edu.tw/handle/123456789/526051
Title: | Adrenoleukodystrophy initially diagnosed as idiopathic Addison's disease in two patients: The importance of early testing | Authors: | WUH-LIANG HWU YIN-HSIU CHIEN Liang J.-S. WANG-TSO LEE Wang P.-J. WEN-YU TSAI |
Issue Date: | 2003 | Journal Volume: | 102 | Journal Issue: | 7 | Start page/Pages: | 510-513 | Source: | Journal of the Formosan Medical Association | Abstract: | Childhood cerebral X-linked adrenoleukodystrophy (X-ALD) is a rare neurodegenerative disease typically presenting from age 4 to 8 years in males. We report 2 cases of X-ALD in boys. The diagnosis of Addison's disease was made before the development of neurological symptoms in both cases. The first patient had hyperpigmentation of the lips and an adrenocoricotropic hormone (ACTH) level higher than 1250 pg/mL when he was 7 years 3 months old. The initial diagnosis was Addison's disease, but X-ALD was diagnosed at age 8 years 8 months, when his motor and mental function deteriorated. The second boy had hypoglycemia, skin pigmentation, and an ACTH level of 1086 pg/mL when he was 4 years 6 months old, but the diagnosis was changed from Addison's disease to X-ALD owing to deterioration in speech at age 7 years. Since both bone marrow transplantation and Lorenzo's oil are beneficial only at the early stage of disease and idiopathic Addison's disease is very rare in children, it is important to test for very-long-chain fatty acids in boys suspected of having Addison's disease. |
URI: | https://www.scopus.com/inward/record.uri?eid=2-s2.0-0346270254&partnerID=40&md5=b46d062ddfd3a2b9e4e317df77c50357 https://scholars.lib.ntu.edu.tw/handle/123456789/526051 |
ISSN: | 0929-6646 | SDG/Keyword: | corticosteroid; corticotropin; cortisone; fludrocortisone; Lorenzo oil; very long chain fatty acid; Addison disease; adrenoleukodystrophy; article; bone marrow transplantation; case report; childhood disease; corticotropin blood level; degenerative disease; diagnostic procedure; diagnostic test; diagnostic value; disease severity; early diagnosis; human; hyperpigmentation; hypoglycemia; idiopathic disease; lip; male; mental function; motor performance; onset age; school child; skin pigmentation; speech; symptomatology; treatment indication; X chromosome linkage; Addison Disease; Adrenoleukodystrophy; Age of Onset; Child; Child, Preschool; Diagnosis, Differential; Humans; Male |
Appears in Collections: | 醫學系 |
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