Results 111 to 120 of about 3,384 (157)

Henoch-schonlein purpura nephritis with renal interstitial lesions

Open Medicine, 2018
To investigate the clinical pathology and prognosis & outcome of Henoch-Schonlein purpura nephritis (HSPN) with renal interstitial lesions.
Liu Feng, Wang Chenyu, Wang Rongzhen, Wang Wenge, Li Min   +4 more
doaj   +1 more source

Henoch–Schönlein purpura induced by sitagliptin: A case report

SAGE Open Medical Case Reports
Dipeptidyl peptidase-4 inhibitors are oral antihyperglycemic medications often used as adjuncts to other antidiabetic agents to treat type 2 diabetes mellitus.
Alexa Moschella, Carly Kirshen
doaj   +1 more source

Henoch Schonlein Purpura – A 5-Year Review and Proposed Pathway [PDF]

, 2012
Henoch Schonlein Purpura (HSP) is the commonest systemic vasculitis of childhood typically presenting with a palpable purpuric rash and frequently involving the renal system.
Beresford, Michael W, Holt, Richard CL, Jones, Caroline A, Richardson, Amanda RW, Watson, Louise   +4 more
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Púrpura de Henoch-Schönlein en el adulto: a propósito de un caso

Revista de la Asociación Colombiana de Dermatología y Cirugía Dermatológica, 2019
La púrpura de Henoch-Schönlein es una vasculitis sistémica de vasos de pequeño calibre. Puede afectar a cualquier órgano, principalmente piel, articulaciones, tracto gastrointestinal y riñón.
Karen Zapata, Ricardo Rueda, Carlos De La Roche   +2 more
doaj  

An adult male with abdominal pain and skin rash

Southwest Respiratory and Critical Care Chronicles, 2014
Henoch-Schönlein purpura is generally a disease of children and uncommon in adults, especially after the age of 40. It is characterized by leukocytoclastic vasculitis skin rash, arthralgia, and gastrointestinal symptoms. In adults, glomerulonephritis may
Jay Patel, Imran Umer, Anand Reddy, Yasir Ahmed, Craig Spellman   +4 more
doaj  

High-dose methylprednisolone pulse therapy for treatment of refractory intestinal involvement caused by Henoch–Schönlein purpura: a case report [PDF]

, 2015

core   +1 more source

Adult onset of Immunoglobulin A vasculitis : A case report [PDF]

, 2019
Immunoglobulin A vasculitis (IgAV), formerly known as Henoch-Schönlein purpura, primarily occurs during childhood between the ages of 3 and 15 years and is the most common form of systemic vasculitis in children ; its occurrence in adults has been rarely
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Henoch-Schonlein purpura. [PDF]

BMJ, 1977
openaire   +1 more source

Methylprednisolone pulse therapy and intravenous cyclophosphamide therapy combined with cocktail therapy in severe pediatric Henoch-Schönlein purpura nephritis patient [PDF]

, 2013
Anna Kobayashi, Emi Sawanobori, Hiroaki Kanai, Kanji Sugita, Kosuke Higashida, Kyoko Matsushita   +5 more
core   +1 more source

A Comparative study: feature and clinical progress of Familial Mediterranean Fever to clinical manifestation onset in 1st decade of life and upper decades [PDF]

BACKGROUND: Familial Mediterranean Fever (FMF) is an autosomal recessive disease characterized by recurrent episode of serositis attack, commonly involving the abdomen, chest or joint, typically accompanied by fever and elevated acute phase reactants ...
حبیب زاده, شهرام, صالح زاده, فرهاد, قیطاسی, اصغر   +2 more
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