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Lymphoid Hyperplasia

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107. The EAU – EANM – ESTRO – ESUR – SIOG Guidelines on Prostate Cancer

and Meta-Analysis. Medicine (Baltimore), 2015. 94: e1260. 45. Rowles, J.L., 3rd, et al. Processed and raw tomato consumption and risk of prostate cancer: a systematic review and dose-response meta-analysis. Prostate Cancer Prostatic Dis, 2018. 21: 319. 46. Ilic, D., et al. Lycopene for the prevention and treatment of benign prostatic hyperplasia and prostate cancer: a systematic review. Maturitas, 2012. 72: 269. 47. Bylsma, L.C., et al. A review and meta-analysis of prospective studies of red (...) Clin Oncol, 2009. 27: 3591. 145. Vickers, A.J., et al. Systematic review of pretreatment prostate-specific antigen velocity and doubling time as predictors for prostate cancer. J Clin Oncol, 2009. 27: 398. 146. Stephan, C., et al. The influence of prostate volume on the ratio of free to total prostate specific antigen in serum of patients with prostate carcinoma and benign prostate hyperplasia. Cancer, 1997. 79: 104. 147. Catalona, W.J., et al. Use of the percentage of free prostate-specific

2020 European Association of Nuclear Medicine

108. Diagnosis of Idiopathic Pulmonary Fibrosis

of a patchy interstitial in?ltrate of lymphocytes and plasma cells associated with hyperplasia of type 2 pneumocytes and bronchiolar epithelium. The ?brotic zones are composed mainly of dense collagen, although scattered convex subepithelial foci of proliferating ?broblasts and myo?broblasts (so-called ?broblast foci) are a consistent ?nding. Microscopic honeycombing is characterized by cystic ?brotic airspaces that are frequently lined by bronchiolar epithelium and ?lled with mucus and in?ammatory cells

2018 American Thoracic Society

109. Inotuzumab ozogamicin (Besponsa) - B-cell precursor acute lymphoblastic leukaemia (ALL)

of age, and approximately 11% of patients are diagnosed after 65 years of age (Howlader et al., 2015). Overall, approximately 20%-30% of adult patients with ALL are Ph+, with the incidence exceeding 50% in patients aged 50 years or older (Jabbour et al., 2015, Thomas DA, 2007). 2.1.3. Biologic features Acute lymphoblastic leukaemia (ALL) is a heterogeneous haematologic disease characterized by the proliferation of immature lymphoid cells in the bone marrow, peripheral blood and other organs resulting

2017 European Medicines Agency - EPARs

111. Guidelines on autopsy practice: Autopsy in sickle cell disease and persons with sickle trait

clinically, it may be useful to remove one femur and split it longitudinally. This enables examination of marrow hyperplasia and sampling of old and recent sites of bone infarction. It can be replaced with leg strut during reconstruction. · Note whether there are skin ulcers on the legs. · Photography: as in any other disease, significantly abnormal organs can be photographed to show clinical and pathology colleagues. [Level of evidence: GPP.] 7 Specific organ systems to be considered All organs (...) disease; new and old ischaemic strokes; intracerebral haemorrhage; subarachnoid haemorrhage; meningitis; dural venous sinus thrombosis · liver: size, congestion, fibrosis, portal vein thrombosis · spleen: the size (tiny remnant to massive sequestration enlargement); infarcts and fibrotic nodules · kidneys: pyelonephritis, papillary necrosis, cortical necrosis · bone marrow: old and new vertebral/long bone infarcts, extent of haemopoietic marrow (hyperplasia); osteomyelitis · biliary system: bile

2017 Royal College of Pathologists

112. Right Lower Quadrant Pain : Suspected Appendicitis

diagnosed with appendicitis on MRI, with 61 of 66 proven pathologically. The 5 false-positive patients had pathologic diagnoses of torsed right ovary (n = 1), appendicolith with mild lymphoid hyperplasia (n = 1), fibrous obliteration of the appendiceal lumen without changes of appendicitis (n = 1), and normal appendices (n = 2). Pooled sensitivity, specificity, accuracy, PPV, and NPV were 96.8%, 99.2%, 99.0%, 92.4%, and 99.7%, respectively. The pooled AUC was 0.98 (95% CI: 0.96-1.0, range 0.83-1 [P (...) and appendectomy. Of these 18 patients, 12 (66.7%) were confirmed, yielding MRI sensitivity of 91.7%, specificity of 95.3%, PPV of 68.8%, and NPV of 99.0%. Of the remaining 6 women who underwent appendectomy, 3 women had no histopathologic abnormality, 1 woman had subserosal histiocytes, 1 woman had fibrous obliteration of the appendiceal lumen, and 1 woman had epithelial hyperplasia and mucocele. An alternate diagnosis on MRI was identified in 74 of 171 (43%) women. Ramalingam et al [61] evaluated

2018 American College of Radiology

114. Tofacitinib (Xeljanz) - Rheumatoid arthritis

Erythropoietin F Female FACS Flourescent activated cell sorting Assessment report EMA/CHMP/853224/2016 Page 4/158 fu Fraction of drug free (unbound) in serum/plasma GALT Gut associated lymphoid tissue GD Gestation Day GFR Glomerular filtration rate GGT Gamma-glutamyltransferase GLP Good Laboratory Practice G-CSF Granulocyte Colony Stimulating Factor GM-CSF Granulocyte-Macrophage Colony Stimulating Factor HCT Hematocrit HDL High density lipoprotein HEK Human embryonic kidney hERG Human ether- à -go-go related (...) cell subsets: T cells with release of T- cell-derived cytokines, production of autoantibodies (rheumatoid factor and anti-citrullinated protein antibody (ACPA) by B cells, and also involves macrophage and fibroblast-like cells which secret large amounts of pro- inflammatory cytokines. 2.1.4. Clinical presentation, diagnosis RA is characterised by synovial inflammation and hyperplasia (“swelling”), autoantibody production, cartilage and bone destruction leading to deformity. It is also often

2017 European Medicines Agency - EPARs

115. BSG and UKPBC primary biliary cholangitis treatment and management guidelines

be of large enough size to view a representative amount of parenchyma and number of portal tracts (proposed to be more than 11). 92 Hallmarks of PBC include destructive granulomatous lymphocytic cholangitis affecting interlobular and septal bile ducts leading to progressive bile duct loss, chronic cholestasis, fibrosis and cirrhosis. Other features that are seen include lymphocytic interface activity, parenchymal necro-inflammation and nodular regenerative hyperplasia. 93 94 The significance of features (...) in the context of clinical trials where liver biopsies have been used for risk stratification and as a surrogate marker of treatment outcomes. (A) Early PBC is characterised mainly by portal lesions and mild necroinflammatory changes in the acini. Portal tracts may show cholangiocentric granulomatous inflammation composed of lymphocytes, occasionally numerous plasmacytes, and polymorphs including eosinophils. Lymphoid follicles with germinal centres may form. The lymphoid inflammatory infiltrate extends

2018 British Society of Gastroenterology

116. Recombinant IGF-1 Therapy in Children with Severe Primary IGF-1 Deficiency

to monitor compliance + * UK IGFD register (NCT00903110); study director Caroline Sert ( E. Maintenance of rhIGF-1 therapy 1. Clinic visits should occur 3-4 monthly for consultant assessment, ideally seeing the same doctor at each visit, and an annual review should be performed. 2. The following targeted adverse events (TAE) should be enquired about at every clinic review and reported through the yellow card scheme AND the IGFD Registry • Hypoglycaemia • Lymphoid Hyperplasia (...) and the demonstration of normal or increased GH secretion. 2. The diagnosis of SPIGFD does not necessarily require a GH stimulation test or an IGF-1 generation test (IGFGT) particularly when the presentation is clearly classical i.e. positive family history, consanguineous pedigree, severe short stature, clinical features of Laron syndrome (mid-facial hyperplasia / fontal bossing), high baseline GH and low or undetectable serum IGF-1. 3. In classic cases, genetic analysis of GHR is recommended in order

2018 British Society for Paediatric Endocrinology and Diabetes

117. CRACKCast E093 – Appendicitis

appendicitis is always found! “In fact, only 40% of patients have the base of their appendix within 3m of McBurney’s point, with 36% of patients having the base more than 5m away.” – These patients can present with pain in the LLQ or the Right flank or in the back (if retrocecal!). Causes: Fecaliths (hard stools) (65%), Appendicoliths (calcified deposits) lymphoid hyperplasia (primary or secondary to an enteric infection). foreign bodies (eg, vegetable matter, inspissated barium), tumors, intestinal

2017 CandiEM

119. Lymphangioleiomyomatosis Diagnosis and Management Part II: An Official ATS/JRS Clinical Practice Guideline

were blinded to clinical and histopathological information. Clinicians included thoracic radiologists (7–9),pulmonologists(9),and pulmonary fellows (9). Diseases included LAM (7–9), pulmonary Langerhans cell histiocytosis (7–9), emphysema (7–9), usual interstitial pneumonia (8), lymphoid interstitial pneumonia (8, 9), desquamative interstitial pneumonia (8), Birt-Hogg-Dub´ e syndrome (9), amyloidosis (9), hypersensitivity pneumonitis (9), nonspeci?c Table 3. Interpretation of Strong and Conditional (...) , relatively uniform, thin-walled cysts in a diffuse distribution. The intervening lung parenchyma often appears normal on HRCT. Other associated features that can be seen on HRCT in some patients with LAM include the presence of: chylous pleural effusion, pneumothorax,ground-glassopacitysuggestiveofchylouscongestion,or multipletinynodulescharacteristicofmultifocalmicronodularpneumocyte hyperplasia (in patients with TSC-LAM). 3 Referral to a TSC center should be considered if there is uncertainty regarding

2017 American Thoracic Society

120. Review of Prader-Willi syndrome: the endocrine approach Full Text available with Trip Pro

therapy until a sleep study can urgently be performed. Lymphoid hyperplasia may theoretically develop due to GH treatment and supra-physiologic IGF-1 levels ( ). Expert opinion recommends maintaining IGF-1 in the upper range of normal for appropriate reference ranges, and titrating GH dose based on IGF-1 levels ( ). Algorithm for growth hormone treatment in PWS. PSG, polysomnography; SDB, sleep disordered breathing; ENT, otolaryngology; T&A, tonsillectomy and adenoidectomy; SCFE, slipped capital

2017 Pediatric Endocrine Society

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