Results 91 to 100 of about 17,217 (221)
Síndrome de Stevens-Johnson e Ibuprofeno [PDF]
Introdução: A síndrome de Stevens-Johnson é uma doença rara com mortalidade de 1 a 5% e morbilidade significativa. Ocorre na sequência de uma reacção de hipersensibilidade imuno-mediada com susceptibilidade individual associada a factores genéticos ...
Brito, MJ, Farela Neves, J, Rodrigues, V
core
ABSTRACT Lorigerlimab is a dual bispecific antibody (BsAb) targeting cytotoxic T‐lymphocyte‐associated protein 4 and programmed cell death protein 1 that is used for treatment of advanced solid cancers such as metastatic castration‐resistant prostate carcinoma.
Niloofar Sina +5 more
wiley +1 more source
Toxic epidermal necrolysis: A review
This article reviews the many facets of toxic epidermal necrolysis. Emphasis is placed on the importance of early diagnosis, burn unit placement, supportive care, and avoidance of systemic steroids. Discussion also includes other therapeutic options and the pathophysiology of the disease.
From the College of Pharmacy, the Division of Dermatology and Cutaneous Surgery ( host institution ) +4 more
openaire +3 more sources
ABSTRACT Stevens–Johnson syndrome and toxic epidermal necrolysis are rare mucocutaneous diseases characterized by widespread epidermal necrosis and a high mortality rate. These conditions are often associated with drug exposure and require complex treatment and nursing care because they cause diverse symptoms in patients.
Zuhal Gulsoy, İclal Özdemir Kol
wiley +1 more source
Skin Detachment and Regrowth in Toxic Epidermal Necrolysis
Toxic epidermal necrolysis is a rare but clinically well-described dermatological pathology. However, clinical pictures of this disorder in text books do not reflect its dynamic evolution.
Laurence Feldmeyer +4 more
doaj +1 more source
Pediatric SJS-TEN: Where are we now? [version 1; peer review: 2 approved]
Stevens–Johnson syndrome and toxic epidermal necrolysis are rare severe blistering skin reactions triggered by medications or infections. Over the last 5 to 10 years, a number of important publications have advanced understanding of these diseases and ...
Michele Ramien, Jennifer L. Goldman
doaj +1 more source
A case of steroid-induced psychosis in a child having nephrotic syndrome with toxic epidermal necrolysis [PDF]
Toxic epidermal necrolysis (TEN) and Stevens–Johnson syndrome (SJS) are rare, life-threatening mucocutaneous diseases, usually attributable to drugs and infections. Corticosteroids have been used in the management of TEN for the
Benyamin +22 more
core +1 more source
ABSTRACT Fluoroquinolones (FQs) are among the most frequently prescribed antibiotic classes worldwide. Despite their therapeutic versatility in treating bacterial infections, regulatory authorities recognized risks of persistent and potentially irreversible adverse effects, particularly peripheral neuropathy (PN).
Nimra Shamim +5 more
wiley +1 more source
Mucocutaneous Manifestation of Systemic Lupus Erythematosus Patients at Rheumatology Outpatient Clinic in Dr. Hasan Sadikin General Hospital [PDF]
Background: Systemic Lupus Erythematosus (SLE) is an autoimmune systemic disease which symptoms induced by Ultraviolet rays exposure. It commonly affects women and causes wide range of symptoms. One of the organs affected is mucocutaneous. Our study aims
Dharmadji, H. P. (Hartati) +3 more
core
Stunted root development: a rare dental complication of Stevens-Johnson syndrome [PDF]
Stevens-Johnson syndrome (SJS) is a severe cutaneous reaction seen rarely in clinical practice. Most often, it occurs as an adverse reaction to certain drugs. When it affects children at a very young age, arrested tooth root development may also be seen.
Dahiya, Parveen +3 more
core +2 more sources

