RESUMO
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.
Assuntos
Insuficiência Adrenal/complicações , Doenças Autoimunes/complicações , Glomerulonefrite Membranosa/complicações , Pancreatite/complicações , Tireoidite Autoimune/complicações , Insuficiência Adrenal/imunologia , Adulto , Especificidade de Anticorpos , Autoanticorpos/sangue , Autoanticorpos/imunologia , Doença Crônica , Feminino , Humanos , Síndrome Nefrótica/etiologia , Pancreatite/imunologiaRESUMO
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