1.A Case of Vogt-Koyanagi-Harada Disease in a Patient With Graves Disease.
Je Hyun SEO ; Hyeong Gon YU ; Hum CHUNG
Korean Journal of Ophthalmology 2009;23(2):112-113
A case of Vogt-Koyanagi-Harada disease (VKH) that developed in a 36-year-old woman with Graves' disease was described. The patient was treated with Lugol's solution and presented with bilateral serous retinal detachment. She had also suffered from methimazole-induced hypersensitivity and steroid-induced myopathy. Fluorescein angiography showed multiple leakage points and a lumbar puncture revealed pleocytosis, which was compatible with VKH. High dose steroid pulse therapy was successful. Altered immune regulation associated with drug-induced hypersensitivity may contribute to the development of VKH in patients with Graves' disease.
Adult
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Coloring Agents/administration & dosage
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Diagnosis, Differential
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Dose-Response Relationship, Drug
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Drug Therapy, Combination
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Female
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Fluorescein Angiography
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Follow-Up Studies
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Fundus Oculi
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Glucocorticoids/administration & dosage
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Graves Disease/*complications/diagnosis/drug therapy
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Humans
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Immunosuppressive Agents/administration & dosage
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Injections, Intravenous
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Iodides/administration & dosage
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Ophthalmic Solutions/administration & dosage
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Uveomeningoencephalitic Syndrome/*complications/diagnosis/drug therapy
2.Graves' disease presenting with acute renal infarction.
Cho Ok BAEK ; Kyung Ae LEE ; Tae Sun PARK ; Heung Yong JIN
The Korean Journal of Internal Medicine 2014;29(6):825-826
No abstract available.
Anticoagulants/therapeutic use
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Antithyroid Agents/therapeutic use
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Graves Disease/*complications/diagnosis/drug therapy
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Humans
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Infarction/diagnosis/drug therapy/*etiology
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Kidney/*blood supply/radiography
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Male
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Middle Aged
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*Thyroid Gland/radionuclide imaging/ultrasonography
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Thyrotoxicosis/diagnosis/drug therapy/*etiology
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Tomography, X-Ray Computed
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Treatment Outcome
3.Neonatal hyperthyroidism: a case report and literature review.
Ning LI ; Xiao-Hua LI ; Ying-Min YAO
Journal of Southern Medical University 2013;33(10):1557-1559
We report a case of neonatal thyrotoxicosis with concurrent respiratory failure in an infant born to a mother with Graves' disease and review the published literature describing neonatal hyperthyroidism. The male infant who was born by spontaneous delivery at 35 weeks of gestational age presented with fever, tachycardia and tachypnea at rest on day 11 after birth, and developed severe apnea on day 14. Thyroid function studies revealed hyperthyroidism in the infant, and his mother was confirmed to have Grave's disease during pregnancy. Literature review showed that among the 33 infants with similar conditions, tachycardia, tachypnea and poor weight gain were the most distinct clinical features of congenital hyperthyroidism. Accurate diagnosis of Graves' disease in the mother during pregnancy and awareness of the clinical presentations of neonatal hyperthyroidism are key to reducing missed diagnosis or misdiagnosis of neonatal hyperthyroidism.
Antithyroid Agents
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therapeutic use
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Apnea
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etiology
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Female
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Graves Disease
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blood
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Humans
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Hyperthyroidism
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blood
;
complications
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diagnosis
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drug therapy
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Infant, Newborn
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Infant, Newborn, Diseases
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blood
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diagnosis
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drug therapy
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Infant, Premature
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Male
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Maternal-Fetal Exchange
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Pregnancy
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Pregnancy Complications
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blood
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Propylthiouracil
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therapeutic use
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Thyrotropin
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blood
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Thyroxine
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blood
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Triiodothyronine
;
blood
4.A Case of Autoimmune Hepatitis Combined with Graves' Disease.
Jong Hyun JHEE ; Hyun Ju KIM ; Wonseok KANG ; Sewha KIM ; Do Young KIM
The Korean Journal of Gastroenterology 2015;65(1):48-51
A 25-year-old woman presented with jaundice, palpitation, and weight loss of 5 kg during a period of 2 weeks. Laboratory tests showed elevated levels of liver enzymes (AST 1,282 IU/L, ALT 1,119 IU/L) and total bilirubin (6.4 mg/dL); negative for hepatitis virus infection; elevated serum levels of triiodothyronine (T3, 3.60 ng/dL), free thyroxine (fT4, 3.82 ng/dL), and lowered serum level of thyroid stimulating hormone (TSH, <0.025 microIU/mL); and positive for thyroid stimulating antibody and anti-mitochondrial antibody (AMA). The liver biopsy findings were consistent with autoimmune hepatitis (AIH). Accordingly, oral steroid therapy was started with 60 mg of prednisolone under the impression of AIH associated with Graves' disease. After a week of steroid therapy, the clinical manifestation showed significant improvement, with normalization of both liver and thyroid functions. Diagnosis of the liver condition of patients who present with hyperthyroidism and liver dysfunction is important, so that appropriate therapy can be promptly initiated.
Adult
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Alanine Transaminase/analysis
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Antibodies, Antinuclear/blood
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Aspartate Aminotransferases/analysis
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Bilirubin/blood
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Female
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Graves Disease/complications/*diagnosis/drug therapy
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Hepatitis, Autoimmune/complications/*diagnosis/drug therapy
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Humans
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Immunoglobulins, Thyroid-Stimulating/blood
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Liver/enzymology/metabolism/pathology
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Prednisolone/therapeutic use
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Steroids/therapeutic use
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Thyrotropin/blood