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Subacute Lymphocytic Thyroiditis

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181. Hyperthyroidism

disease, toxic solitary and multinodular goiters usually do not remit. Inflammatory thyroid disease (thyroiditis) includes subacute granulomatous thyroiditis, Hashimoto thyroiditis, and , a variant of Hashimoto thyroiditis. Hyperthyroidism is more common in subacute granulomatous thyroiditis and results from destructive changes in the gland and release of stored hormone, not from increased synthesis. Hypothyroidism may follow. Inappropriate TSH secretion is a rare cause. Patients with hyperthyroidism (...) of the Endocrine System Which of the following hormones regulates gene function and interacts with receptors inside cells? Antidiuretic hormone Growth hormone Thyroid hormone Thyrotropin-releasing hormone NEWS & VIDEOS Endogenous Testosterone Linked to Cardiovascular Disease THURSDAY, March 7, 2019 (HealthDay News) -- In men, endogenous testosterone may have a causal role in thromboembolism, heart failure, and myocardial infarction, according to a study published... 3D Model Female Endocrine System Video

2013 Merck Manual (19th Edition)

182. Paraneoplastic Syndromes

thyroid carcinoma), and thyroid-stimulating hormone (from gestational choriocarcinoma). PTHRP causes hypercalcemia and its associated symptoms (polyuria, dehydration, constipation, muscle weakness); calcitonin causes a fall in the serum calcium level, leading to muscle twitching and cardiac arrhythmias. GI paraneoplastic syndromes Watery diarrhea with subsequent dehydration and electrolyte imbalances may result from tumor-related secretion of prostaglandins or vasoactive intestinal peptide. Implicated (...) or cell lines. Neurologic paraneoplastic syndromes Several types of peripheral neuropathy are among the neurologic paraneoplastic syndromes. Cerebellar syndromes and other central neurologic paraneoplastic syndromes also occur. Peripheral neuropathy is the most common neurologic paraneoplastic syndrome. It is usually a distal sensorimotor polyneuropathy that causes mild motor weakness, sensory loss, and absent distal reflexes. Subacute sensory neuropathy is a more specific but rare peripheral

2013 Merck Manual (19th Edition)

183. List of cutaneous conditions

symmetric lipomatosis of Launois–Bensaude, Madelung's disease) (centrifugal lipodystrophy, lipodystrophia centrifugalis abdominalis infantalis) (erythema nodosum migrans, subacute migratory panniculitis of Vilanova and Piñol, subacute nodular migratory panniculitis) (popsicle panniculitis) (Berardinelli–Seip syndrome) (Köbberling–Dunnigan syndrome) (Ferreira–Marques lipoatrophia) (semicircular lipoatrophy) (chronic panniculitis with lipomembranous changes, hypodermitis sclerodermiformis, sclerosing (...) : Endocrine conditions often present with cutaneous findings as the interacts with the in many ways. (acanthosis nigricans type I) (acanthosis nigricans type III) (acral acanthotic anomaly) (ANOTHER syndrome) (ovarian SAHA syndrome) (acanthosis nigricans type II) (HAIR-AN syndrome) (Wermer syndrome) (multiple endocrine neoplasia type 2A, pheochromocytoma and amyloid-producing medullary thyroid carcinoma, PTC syndrome, Sipple syndrome) (mucosal neuromata with endocrine tumors, multiple endocrine neoplasia

2012 Wikipedia

184. ACC/AHA/ESC 2006 Guidelines for Management of Patients With Ventricular Arrhythmias and the Prevention of Sudden Cardiac Death

8.4.1.2. Rheumatic disease . . 782 8.4.1.3. Endocarditis 782 8.4.2. In?ltrative cardiomyopathies . 783 8.4.2.1. Sarcoidosis 783 8.4.2.2. Amyloidosis 783 8.4.2.3. Fabry disease 783 8.4.2.4. Hemochromatosis 783 8.4.3. Endocrine disorders and diabetes 783 8.4.3.1. Introduction. 783 8.4.3.2. Thyroid disorders 784 8.4.3.3. Pheochromocytoma 784 8.4.3.4. Acromegaly . 784 8.4.3.5. Primary aldosteronism, addison disease, hyperparathyroidism, and hypoparathyroidism . . . . . . 784 8.4.3.6. Diabetes 784 8.4.4

2006 European Society of Cardiology

185. 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

186. 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

187. Paraneoplastic autoimmune optic neuritis with retinitis defined by CRMP-5-IgG. (Abstract)

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

188. Painful Hashimoto's thyroiditis as an indication for thyroidectomy: clinical characteristics and outcome in seven patients. Full Text available with Trip Pro

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

2003 Journal of Clinical Endocrinology and Metabolism

189. Papillary carcinoma obscured by complication with subacute thyroiditis: sequential ultrasonographic and histopathological findings in five cases. (Abstract)

Papillary carcinoma obscured by complication with subacute thyroiditis: sequential ultrasonographic and histopathological findings in five cases. Subacute thyroiditis (SAT) has been rarely reported to coexist with thyroid carcinomas. The objective of the study was to assess sequential ultrasonographic and histopathological findings of SAT in the context of complicating thyroid carcinomas.Of 1152 patients with SAT who visited our thyroid clinic at Kuma Hospital from 1996 through 2006, 5 cases (...) complicated by papillary carcinoma underwent surgical resection 3-16 months after SAT onset. Ultrasonographic examinations and thyroid function tests were performed in all patients at onset of SAT and just before surgery. Sequential histopathological features of regenerated thyroid and carcinoma involvement were evaluated.Heterogenous areas with microcalcifications in the thyroid or lymphadenopathy in three patients were clues for the nodular involvement with papillary carcinoma on the initial

2008 Thyroid

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