Results 121 to 130 of about 89,434 (295)
Use of Plasmapheresis and Immunosuppressants to Treat Diffuse Alveolar Hemorrhage in a Patient with Granulomatosis with Polyangiitis. [PDF]
, 2019 Granulomatosis with polyangiitis (GPA) is a systemic granulomatous inflammatory disease characterized by small-to-medium vessel vasculitis due to Central Anti-Neutrophil Cytoplasmic Antibody (C-ANCA).
Sattar, Yasar +4 more
core +1 more source
JPGN Reports, EarlyView.Abstract Ustekinumab (UST) is a monoclonal antibody used in the management of moderate to severe inflammatory bowel disease. While generally well‐tolerated, serious adverse reactions, including hypersensitivity and anaphylaxis, have been documented, specifical following the initial intravenous (IV) dose.
Kennedy Sparling +2 more
wiley +1 more source
Mouse model of Schistosomiasis: infection with Schistosoma mansoni in CD-1 mice [PDF]
, 2019 Schistosomiasis is a parasitic disease that affects almost 240 million worldwide. CD1 mice were infected with cercariae of S. mansoni, after which infection developed for 8 weeks. Tissues were processed to immuno-histological techniques.
Botelho, M. +3 more
core
Gastric antral vascular ectasia: A rare etiology of gastrointestinal bleeding in children
JPGN Reports, EarlyView.Abstract Gastrointestinal bleeding is relatively common in children. While most patients present with mild bleeding, gastric antral vascular ectasia (GAVE) is a rare but potentially life‐threatening cause. GAVE is typically associated with chronic conditions and more common in adults.
Omar Alharbi +3 more
wiley +1 more source
The Rare Presentation of Deep Dermatophytosis‐Trichophyton in an Immunosuppressed Patient
JEADV Clinical Practice, EarlyView.ABSTRACT Dermatophytes typically cause superficial skin infections characterized by an active border. However, they can present atypically invading deeper in immunocompromised patients. We present a case of a 72‐year‐old woman with bullous pemphigoid who had received oral prednisolone for 3 months and developed umbilicated papules.
Jidapa Triwatcharikorn +3 more
wiley +1 more source
BCGiosis as a presenting feature of a child with chronic granulomatous disease
Brazilian Journal of Infectious DiseasesBacillus Calmette Guerin (BCG) vaccine, which is administered to all newborns in some regions, could lead to serious complication ranging from local disease (known as BCGitis) to disseminated disease (BCGosis) in a group of patients with primary ...
Zahra Movahedi +3 more
doaj +1 more source
Low Dose Pegylated Interferon Alpha as a First‐Line Treatment for Necrobiotic Xanthogranuloma
JEADV Clinical Practice, EarlyView.ABSTRACT Necrobiotic xanthogranuloma (NXG) is a rare, progressive granulomatous disorder frequently associated with monoclonal gammopathy, particularly monoclonal gammopathy of undetermined significance (MGUS). It typically presents with indurated to ulcerative yellowish plaques or nodules, often with ocular involvement.
Ishana Dixit +2 more
wiley +1 more source
Successful Treatment of Paediatric Necrobiosis Lipoidica With Baricitinib
JEADV Clinical Practice, EarlyView.ABSTRACT Necrobiosis lipoidica (NL) is a rare, chronic granulomatous condition that typically presents as sharply demarcated plaques with telangiectasia and atrophic centres. Paediatric cases are uncommon, and treatment options often fail to address refractory cases.
P. Simões Farinha, M. J. Paiva‐Lopes
wiley +1 more source
Gastric antral stricture in a patient with chronic granulomatous disease
The Turkish Journal of Pediatrics, 1999 Chronic granulomatous disease (CGD) is a rare disorder of phagocytic cell oxidative metabolism. Patients have recurrent infections with catalase-positive organisms and granulomatous lesions throughout the body. Gastric antrum can be an occult site
A Metin +4 more
doaj
Chronic granulomatous disease: Case series
Pediatric Hematology Oncology Journal, 2016 Purva Kanvinde +11 more
doaj +1 more source