Sarcoidosis in children
Identifieur interne : 003417 ( Main/Exploration ); précédent : 003416; suivant : 003418Sarcoidosis in children
Auteurs : P. J. Robinson [Australie] ; A. Olinsky [Australie]Source :
- Journal of Paediatrics and Child Health [ 1034-4810 ] ; 1986-11.
English descriptors
- Teeft :
- Abnormal liver function tests, Anorexia, Biopsy, Characteristic granulomas, Chest radiograph, Clinical course, Clinical picture, Corticosteroid, Corticosteroid therapy, Hepatomegaly, Hypercalcaemia, Laboratory investigations, Lung biopsy, Lung disease, Lymphadenopathy, Melbourne, Node, Normal range, Olinsky, Paediatric, Paediatric patients, Paediatric sarcoidosis, Peripheral lymphadenopathy, Previous studies, Radiograph, Royal hospital, Sarcoidosis, Serial measurements, Serum enzyme activity, Skin biopsy, Steroid, Steroid therapy, System involvement, Thoracic medicine, Tissue biopsies, Tissue biopsy, Weight loss.
Abstract
Abstract Eight patients with sarcoidosis seen at the Royal Children's Hospital, Melbourne, during the past 10 years were reviewed. Five of the eight patients came form non‐metropolitan areas. The major presenting symptoms were cough, fatigue and weight loss; peripheral lymphadenopathy and hepatomegaly were common. None of the patients had eye or central nervous system involvement. Seven patients had bilateral hilar adenopathy on chest radiography and six had parenchymal lung changes. Angiotensin converting enzyme was measured in six patients and was elevated in all, while hypercalcaemia was present in three patients. Five patients had a tissue biopsy showing the characteristic non‐caseating granulomas. Corticosteroid therapy was used for four patients and was given for hypercalcaemia in three patients and for severe restrictive lung disease in one patient.
Url:
DOI: 10.1111/j.1440-1754.1986.tb02150.x
Affiliations:
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Le document en format XML
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<term>Biopsy</term>
<term>Characteristic granulomas</term>
<term>Chest radiograph</term>
<term>Clinical course</term>
<term>Clinical picture</term>
<term>Corticosteroid</term>
<term>Corticosteroid therapy</term>
<term>Hepatomegaly</term>
<term>Hypercalcaemia</term>
<term>Laboratory investigations</term>
<term>Lung biopsy</term>
<term>Lung disease</term>
<term>Lymphadenopathy</term>
<term>Melbourne</term>
<term>Node</term>
<term>Normal range</term>
<term>Olinsky</term>
<term>Paediatric</term>
<term>Paediatric patients</term>
<term>Paediatric sarcoidosis</term>
<term>Peripheral lymphadenopathy</term>
<term>Previous studies</term>
<term>Radiograph</term>
<term>Royal hospital</term>
<term>Sarcoidosis</term>
<term>Serial measurements</term>
<term>Serum enzyme activity</term>
<term>Skin biopsy</term>
<term>Steroid</term>
<term>Steroid therapy</term>
<term>System involvement</term>
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<front><div type="abstract" xml:lang="en">Abstract Eight patients with sarcoidosis seen at the Royal Children's Hospital, Melbourne, during the past 10 years were reviewed. Five of the eight patients came form non‐metropolitan areas. The major presenting symptoms were cough, fatigue and weight loss; peripheral lymphadenopathy and hepatomegaly were common. None of the patients had eye or central nervous system involvement. Seven patients had bilateral hilar adenopathy on chest radiography and six had parenchymal lung changes. Angiotensin converting enzyme was measured in six patients and was elevated in all, while hypercalcaemia was present in three patients. Five patients had a tissue biopsy showing the characteristic non‐caseating granulomas. Corticosteroid therapy was used for four patients and was given for hypercalcaemia in three patients and for severe restrictive lung disease in one patient.</div>
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