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1.
Nefrologia ; 24(4): 376-9, 2004.
Article in Spanish | MEDLINE | ID: mdl-15455500

ABSTRACT

A 33 year old female was admitted to the hospital to study aedema and bocio, A nephrotic syndrome was diagnosed and the renal biopsy demonstrated membranous glomerulonephritis, stage II. She was also diagnosed of Hashimoto's autoinmmune thyroiditis: TSH (41.5 uUl/ml), T4 (0.07 ng/dl), antithyroglobuline (1/2560) and antimicrosome (1/6400). Four year latter she was diagnosed of autoinmmune pancreatitis, without evidence of diabetes mellitus or exocrine pancreatic insufficiency. Eight years latter she was diagnosed of primary autoimmune suprarrenal insufficiency: basal cortisol: 2.7 mcg/dl, post ACTH estimulated cortisol: 5.6 mcg/dl, antinuclear antibody (1/160) and antiparietal (1/320). We present a pluriglandular autoimmune syndrome with membranous glomerulonephritis, thyroiditis, pancreatitis and suprarrenal insufficiency. To the best of our knowledge this complex syndrome has not been previously described.


Subject(s)
Adrenal Insufficiency/complications , Autoimmune Diseases/complications , Glomerulonephritis, Membranous/complications , Pancreatitis/complications , Thyroiditis, Autoimmune/complications , Adrenal Insufficiency/immunology , Adult , Antibody Specificity , Autoantibodies/blood , Autoantibodies/immunology , Chronic Disease , Female , Humans , Nephrotic Syndrome/etiology , Pancreatitis/immunology
2.
Rev Esp Enferm Dig ; 96(9): 667, 2004 Sep.
Article in Spanish | MEDLINE | ID: mdl-15643715
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