Osteomalacia revealing celiac disease and primary biliary cirrhosis-related Fanconi syndrome in a patient with systemic sclerosis

Détails

ID Serval
serval:BIB_F6F8BCAD3980
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
Osteomalacia revealing celiac disease and primary biliary cirrhosis-related Fanconi syndrome in a patient with systemic sclerosis
Périodique
Clin Exp Rheumatol
Auteur⸱e⸱s
Terrier B., Fakhouri F., Berezne A., Bouldouyre M. A., Guilpain P., Sogni P., Terris B., Noel L. H., Guillevin L., Mouthon L.
ISSN
0392-856X (Print)
ISSN-L
0392-856X
Statut éditorial
Publié
Date de publication
2008
Volume
26
Numéro
3
Pages
467-70
Langue
anglais
Notes
Terrier, B
Fakhouri, F
Berezne, A
Bouldouyre, M-A
Guilpain, P
Sogni, P
Terris, B
Noel, L-H
Guillevin, L
Mouthon, L
eng
Case Reports
Italy
Clin Exp Rheumatol. 2008 May-Jun;26(3):467-70.
Résumé
Systemic sclerosis (SSc) may affect the gastrointestinal tract and cause very rarely malabsorption syndrome related to bacterial overgrowth. Malabsorption syndrome may be responsible for weight loss, diarrhea, osteomalacia, and iron and vitamins deficiency. We report the case of a SSc patient who developed osteomalacia caused by the combination of two exceptional conditions in the setting of SSc: celiac disease (CD) and primary biliary cirrhosis (PBC)-related Fanconi syndrome. Oral prednisone with angiotensin-converting enzyme inhibitors, was initiated because of active lesions of tubulitis, and led to the complete regression of bone pains, and by the improvement of renal function and regression of the features of proximal tubulopathy. Thus, in the presence of vitamin deficiencies in a patient with SSc, together with a search for malabsorption syndrome secondary to bacterial overgrowth, CD and/or PBC-associated Fanconi syndrome should be investigated.
Mots-clé
Adult, Celiac Disease/*complications/diagnosis, Fanconi Syndrome/*complications/diagnosis, Female, Humans, Liver Cirrhosis, Biliary/*complications/diagnosis, Osteomalacia/diagnosis/*etiology, Scleroderma, Systemic/*complications
Pubmed
Création de la notice
01/03/2022 11:18
Dernière modification de la notice
02/03/2022 7:36
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