minocycline has been researched along with Graves-Disease* in 2 studies
2 other study(ies) available for minocycline and Graves-Disease
Article | Year |
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Minocycline-induced drug hypersensitivity syndrome followed by multiple autoimmune sequelae.
Drug hypersensitivity syndrome (DHS) is a severe, multisystem adverse drug reaction that may occur following the use of numerous medications, including anticonvulsants, sulfonamides, and minocycline hydrochloride. Long-term autoimmune sequelae of DHS have been reported, including hypothyroidism.. A 15-year-old female adolescent developed DHS 4 weeks after starting minocycline therapy for acne vulgaris. Seven weeks later she developed autoimmune hyperthyroidism (Graves disease), and 7 months after discontinuing minocycline therapy she developed autoimmune type 1 diabetes mellitus. In addition, she developed elevated titers of several markers of systemic autoimmune disease, including antinuclear, anti-Sjögren syndrome A, and anti-Smith antibodies.. Minocycline-associated DHS may be associated with multiple autoimmune sequelae, including thyroid disease, type 1 diabetes mellitus, and elevated markers of systemic autoimmunity. Long-term follow-up is needed in patients with DHS to determine the natural history of DHS-associated sequelae. Topics: Acne Vulgaris; Adolescent; Anti-Bacterial Agents; Autoimmune Diseases; Diabetes Mellitus, Type 1; Drug Hypersensitivity; Female; Graves Disease; Humans; Minocycline | 2009 |
Pyoderma gangrenosum with secondary pyarthrosis following propylthiouracil.
The association of pyoderma gangrenosum and arthritic symptoms is well documented. We present a rarely reported variant of this in a 44-year-old woman with pyoderma gangrenosum and bilateral large purulent effusions of her knees. She had no evidence of underlying rheumatoid arthritis or a specific seronegative spondyloarthropathy. Of note she had a history of Graves' disease for which she had been treated with propylthiouracil for 3 years and on investigation at this presentation had a markedly elevated perinuclear antineutrophil cytoplasm antibody (P-ANCA) level with specificities for IgM myeloperoxidase, IgG elastase and IgG lactoferrin. We believe this patient had pyoderma gangrenosum with secondary sterile pyarthrosis and a P-ANCA precipitated by propylthiouracil. Topics: Adult; Antibodies, Antineutrophil Cytoplasmic; Antimetabolites; Arthritis, Reactive; Female; Graves Disease; Humans; Minocycline; Prednisolone; Propylthiouracil; Pyoderma Gangrenosum; Skin | 1999 |