Results 141 to 150 of about 128,191 (326)
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
Pathological manifestations of granulomatous lobular mastitis
Granulomatous lobular mastitis (GLM) is a rare inflammatory breast disease with unknown etiology, characterized by non-caseous granulomatous inflammation of the lobules, which infiltrate lymphocytes, neutrophils, plasma cells, monocytes, and eosinophils ...
Leyin Cui +5 more
doaj +1 more source
BCG-LYMPHADENITIS IN CHILDREN WITH CHRONIC GRANULOMATOUS DISEASE. 74 [PDF]
M Sarbinova +4 more
openalex +1 more source
Sarcoidosis versus Granulomatous and Lymphocytic Interstitial Lung Disease in Common Variable Immunodeficiency: A Comparative Review [PDF]
Helena Buso +12 more
openalex +1 more source
Gastric antral vascular ectasia: A rare etiology of gastrointestinal bleeding in children
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
Report of 2 Cases of Chronic Granulomatous Disease in Adults
Introduction: Chronic granulomatous disease (CGD) is an inherited disorder of phagocyte function . The defect of intracellular killing in phagocytes is the cause of recurrent pyogenic infection of patients .
Mahdi Eskandarlou +5 more
doaj
The Rare Presentation of Deep Dermatophytosis‐Trichophyton in an Immunosuppressed Patient
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

