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185 results for

Subacute Lymphocytic Thyroiditis

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181. Childhood and Congenital Hypothyroidism

function can occur. [ ] If treatment is delayed, spasticity, gait problems and dysarthria and profound mental disability may result. Poor self-esteem and depression are amongst several factors that lead to a poorer quality of life in patients who have been treated for CH. [ ] A high index of suspicion with careful questioning is required to pick up on these aspects. Acquired childhood hypothyroidism The most common cause of childhood hypothyroidism is lymphocytic thyroiditis, also known (...) be iatrogenic (eg, treatment for hyperthyroidism). Rarer causes include acute suppurative thyroiditis and subacute non-suppurative thyroiditis (de Quervain's disease). Subclinical hypothyroidism (SH) in children This is quite common in children and adolescents. It is a remitting process with a low risk of evolution toward overt hypothyroidism. See separate article . Did you find this information useful? Thanks for your feedback! Why not subscribe to the newsletter? Email address * We'd love to send you our

2008 Mentor

182. thyroiditis

thyroiditis thyroiditis - General Practice Notebook This site is intended for healthcare professionals General Practice Notebook | Medical search thyroiditis The most common and well characterised forms of thyroiditis are: Hashimoto's or autoimmune thyroiditis De Quervains or subacute granulomatous thyroiditis subacute lymphocytic or painless thyroiditis Riedel's thyroiditis Less common and less characterised forms are: acute or infective thyroiditis infiltrative thyroiditis e.g. sarcoidosis

2010 GP Notebook

183. ACC/AHA/ESC 2006 Guidelines for Management of Patients With Ventricular Arrhythmias and the Prevention of Sudden Cardiac Death Rheumatic disease . . 782 Endocarditis 782 8.4.2. In?ltrative cardiomyopathies . 783 Sarcoidosis 783 Amyloidosis 783 Fabry disease 783 Hemochromatosis 783 8.4.3. Endocrine disorders and diabetes 783 Introduction. 783 Thyroid disorders 784 Pheochromocytoma 784 Acromegaly . 784 Primary aldosteronism, addison disease, hyperparathyroidism, and hypoparathyroidism . . . . . . 784 Diabetes 784 8.4.4

2006 European Society of Cardiology

184. Paraneoplastic autoimmune optic neuritis with retinitis defined by CRMP-5-IgG. (PubMed)

autopsied patient had predominantly CD8(+) T lymphocytes infiltrating optic nerve and spinal cord. Eleven patients had confirmed small-cell carcinoma; 1 had imaging evidence of lung cancer; 3 had renal or thyroid carcinoma. Full-length CRMP-5 protein was identified in normal retina and optic nerve by Western blot analyses. Photoreceptor cells, retinal ganglion cells, and nerve fibers exhibited CRMP-5-specific immunoreactivity. In summary, CRMP-5-IgG defines a paraneoplastic ophthalmological entity (...) Paraneoplastic autoimmune optic neuritis with retinitis defined by CRMP-5-IgG. Autoantibodies have defined two paraneoplastic visual disorders related to small-cell lung carcinoma: retinopathy ("CAR"-IgG [23kDa, recoverin]) and optic neuritis collapsin response-mediated protein 5 (CRMP-5-IgG [62kDa]). Among 16 patients with CRMP-5-IgG and optic neuritis (aged 52-74 years; all smokers, 9 women), we documented coexisting retinitis in 5. None had CAR-IgG. Fifteen had subacute vision loss, swollen

2003 Annals of Neurology

185. Painful Hashimoto's thyroiditis as an indication for thyroidectomy: clinical characteristics and outcome in seven patients. (PubMed)

Painful Hashimoto's thyroiditis as an indication for thyroidectomy: clinical characteristics and outcome in seven patients. Patients with chronic lymphocytic thyroiditis, or Hashimoto's thyroiditis (HT), usually present with goiter, hypothyroidism, or both. Thyroid pain and tenderness are rare and suggest an alternative diagnosis of subacute granulomatous thyroiditis or other forms of thyroiditis. We report seven patients with painful HT who had temporary or no relief from L-thyroxine (...) replacement or steroid treatment and required surgical intervention for unremitting pain. Antithyroid antibodies were elevated in all except one patient, in whom fine-needle aspiration and surgical pathology were diagnostic of HT. All patients underwent either a subtotal or near-total thyroidectomy. Pathology showed lymphocytic thyroiditis in all specimens, with varying degrees of fibrosis. Giant cells and granulomas characteristic of subacute thyroiditis were not seen. After surgery, four patients

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2003 Journal of Clinical Endocrinology and Metabolism

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