Results 131 to 140 of about 201,611 (277)

The profile and clinical outcomes of patients with renal involvement due to IgA vasculitis: is azathioprine a good option for treatment?

Advances in Rheumatology, 2019
Background The Henoch-Schönlein Purpura (HSP) orIgA vasculitis is the most common vasculitis of childhood and may occur with renal involvement, with hematuria and / or proteinuria, and may cause severe and non-reversible sequelae. Objectives To establish
Vânia Schinzel, Jade Dib Fernandez, Gleice Clemente, Melissa Mariti Fraga, Maria Cristina Andrade, Claudio Arnaldo Len, Maria Teresa Terreri   +6 more
doaj   +1 more source

Multiple esophageal ulcers in a pediatric case of granulomatosis with polyangiitis: A case report

DEN Open, Volume 5, Issue 1, April 2025.
Abstract A 14‐year‐old girl presented with diarrhea and bloody stools was initially diagnosed with infectious colitis and anal fissure. The patient was treated with antibiotics; however, the symptoms persisted and purpura appeared on the patient's lower abdomen. Abdominal computed tomography indicated diffuse wall thickening of the entire colon.
Yuki Kimura, Takashi Ishige, Takuya Nishizawa, Yoshiko Igarashi, Yoshihito Saito, Ryusuke Yagi, Maiko Tatsuki, Reiko Hatori, Hayato Ikota, Takumi Takizawa   +9 more
wiley   +1 more source

Inflammatory bowel disease-specific autoantibodies in HLA-B27-associated spondyloarthropathies: Increased prevalence of ASCA and pANCA [PDF]

, 2004
Aims: An association between inflammatory bowel disease (IBD) and spondyloarthropathies (SpA) has repeatedly been reported. The aim of the present study was to investigate whether serologic markers of IBD, e. g.
Brumberger, V., Folwaczny, Christian, Glas, J., Gruber, R., Kellner, H., Marker-Hermann, E., Strasser, C., Török, H.-P.   +7 more
core   +1 more source

Systematic Review of Management Strategies for Alport Syndrome: Implications for Male Patients

Health Science Reports, Volume 8, Issue 4, April 2025.
ABSTRACT Background and Aims Alport Syndrome (AS) is a rare genetic disorder characterized by progressive kidney disease, hearing loss, and ocular abnormalities, with an incidence of approximately 1 in 50,000 newborns. Due to the severity of the disease, particularly in males with X‐linked inheritance, this systematic review consolidates current ...
Zouina Sarfraz, Ayesha Khan, Maryyam Liaqat, Aden Khan, Faheem Javad, Meher Saleem, Azza Sarfraz, Musfira Khalid, Muzna Sarfraz, Manish Kc, Omar Irfan   +10 more
wiley   +1 more source

Navigating the initial diagnosis and management of adult IgA vasculitis: A reviewCapsule Summary

JAAD International, 2022
Background: IgA vasculitis in adults has not been thoroughly studied. This has left a practice gap related to the management and follow-up of a population that is at an increased risk of comorbidities and potentially poor outcomes. For this reason, it is
Brenna G. Kelly, BA, Delaney B. Stratton, PhD, DNP, FNP-BC, Iyad Mansour, MD, Bekir Tanriover, MD, MPH, MBA, Keliegh S. Culpepper, MD, Clara Curiel-Lewandrowski, MD   +5 more
doaj  

Do We Need Distinct Pediatric Classification Criteria for Rheumatic Diseases That Affect Both Children and Adults?

Arthritis &Rheumatology, Volume 77, Issue 5, Page 521-525, May 2025.
Coziana Ciurtin, Marija Jelusic, Seza Ozen   +2 more
wiley   +1 more source

Drug‐Induced Renal Vasculitis: Etiology, Pathogenesis, Clinical Manifestations, and Therapeutic Approaches—A Narrative Review

Health Science Reports, Volume 8, Issue 4, April 2025.
ABSTRACT Background and Aims Drug‐induced renal vasculitis arises from various medications that cause immunological dysregulation or direct vascular damage, leading to inflammation and thrombosis. Clinical manifestations vary widely, from mild constitutional symptoms to severe organ dysfunction. This review aims to thoroughly explore drug‐induced renal
Hashim Mohamed Siraj, Masab Ali, Sampda Sanjaykumar Sharma, Afreen Begum, Muhammad Husnain Ahmad, Muhammad Hassan, Roba Kamaleldin Moustafa Kamel Aref Elsayed, Muhammad Hamza Tahir   +7 more
wiley   +1 more source

Myeloperoxidase-Antineutrophil Cytoplasmic Antibody-Negative Microscopic Polyangiitis with Pulmonary Haemorrhage and IgA Nephropathy [PDF]

, 2011
Aim: To report a case of a patient with myeloperoxidase-antineutrophil cytoplasmic antibody (ANCA)-negative microscopic polyangiitis (MPA) and IgA nephropathy associated with severe pulmonary haemorrhage.
Endo, Yuichiro, Kato, Mayumi, Kore-Eda, Satoshi, Minato, Haruka, Miyachi, Yoshiki, Taki, Reiko, Tanioka, Miki   +6 more
core   +3 more sources

Cutaneous‐limited, initially strongly unilateral microscopic polyangiitis

JDDG: Journal der Deutschen Dermatologischen Gesellschaft, Volume 23, Issue 5, Page 650-653, May 2025.
Roman Saternus, Thomas Vogt, Zanir Abdi
wiley   +1 more source

Iron Deficiency Anemia: An Unexpected Cause of an Acute Occipital Lobe Stroke in an Otherwise Healthy Young Woman [PDF]

, 2020
A 29-year-old caucasian woman who presented to the hospital with an acute onset of right eye visual disturbance and headache was found to have an acute left occipital lobe infarction.
Nace, Travis C, O\u27Sullivan, Conor, Shan, Khine S, Zhang, Qian   +3 more
core   +1 more source