Results 41 to 50 of about 1,250 (186)

Acute febrile neutrophilic dermatosis, post COVID-19. Case presentation [PDF]

open access: yes, 2022
Introducere. Dermatoza acută neutrofilică febrilă, denumită și sindromul Sweet, reprezintă o afecțiune rară, manifestată clinic prin erupție cutanată tip eritem polimorf, însoțită de febră până la 40°C și leucocitoză neutrofilică.
Iacovlev, Irina   +4 more
core  

Sweet Syndrome in childhood [PDF]

open access: yesAnais Brasileiros de Dermatologia, 2015
Sweet syndrome or acute febrile neutrophilic dermatosis is a recurrent and rare skin disease caused by the release of cytokines, with diverse possible etiologic causes.
Talita Batalha Pires dos Santos   +4 more
doaj   +2 more sources

A Case of Acute Myeloid Leukemia-Associated Necrotizing Sweet Syndrome

open access: yesCase Reports in Dermatology, 2022
Sweet syndrome (SS), or acute febrile neutrophilic dermatosis, is a rare painful skin condition that is characterized by hyperpyrexia, peripheral blood and skin neutrophilia, and edematous skin lesions.
Jennifer Strong   +12 more
doaj   +1 more source

Refractory neuro-Sweet disease successfully treated with tocilizumab and mycophenolate mofetil [PDF]

open access: yesEncephalitis, 2021
Sweet syndrome, or acute febrile neutrophilic dermatosis, is mainly a dermatologic condition presenting with erythematous plaques; however, neutrophils infiltrate multiple systems. Neuro-Sweet disease is a neurological manifestation of Sweet syndrome and
Sungeun Hwang   +7 more
doaj   +1 more source

Sweet Syndrome in a Patient with Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma: Curious Lymphocyte/Neutrophil Fluctuations

open access: yesTurkish Journal of Hematology, 2013
Sweet syndrome, also referred to as acute febrile neutrophilic dermatosis, is characterized by tender, red inflammatory nodules or papules that occur in association with infection, malignancy, connective tissue disease, or following exposure to certain ...
Çiğdem Usul Afşar   +6 more
doaj   +1 more source

Cryptococcoid Sweet syndrome: a case report

open access: yesFrontiers in Medicine
Cryptococcoid Sweet syndrome (cSS) is a recently described clinical and histological variant of Sweet syndrome (SS). Its cutaneous presentation is similar to the classical form of SS but it includes atypical findings, such as capsular and yeast-like ...
Martina Volonté   +9 more
doaj   +1 more source

Sweet’s syndrome and fistulizing Crohn’s disease: A case report

open access: yesSAGE Open Medical Case Reports, 2019
Sweet’s syndrome is a rare, acute febrile neutrophilic dermatosis sometimes associated with inflammatory diseases, infections, malignancies or the administration of pharmacotherapeutics. Very seldom, it occurs as an extraintestinal manifestation of Crohn’
Stefan T Siedlikowski, Julie D Lacroix
doaj   +1 more source

IDH1 inhibitor-induced neutrophilic dermatosis in a patient with acute myeloid leukemia

open access: yesCancer Treatment and Research Communications, 2022
Ivosidenib is an oral inhibitor of mutant Isocitrate dehydrogenase 1 (IDH1). It is approved for treatment of patients with relapsed or refractory IDH1-mutated acute myeloid leukemia (AML) and patients with newly diagnosed IDH1-mutated AML who are 75 ...
Sydney Dunn-Valadez   +8 more
doaj   +1 more source

Atypical Persistent Pruritic Hyperpigmented Plaques in Adult‐Onset Still's Disease: A Case Report From Uganda

open access: yesClinical Case Reports, Volume 14, Issue 5, May 2026.
Atypical Persistent hyperpigmented cutaneous lesions associated with adult‐onset Still's disease. ABSTRACT We report a case of adult‐onset Still's disease (AOSD) in a 30‐year‐old Ugandan man presenting with migratory polyarthralgia, intermittent fever, lymphadenopathy, and atypical persistent pruritic hyperpigmented plaques.
Abdisalam Ahmed Sandeyl   +7 more
wiley   +1 more source

Uncovering the Genetic Landscape of Spinal Dysraphism: A Retrospective Analysis of 150 Fetal Cases

open access: yesPrenatal Diagnosis, Volume 46, Issue 5-6, Page 849-861, May 2026.
ABSTRACT Objective Spinal dysraphism (SD) results from incomplete neural tube closure and encompasses a heterogeneous group of congenital anomalies with genetic and environmental etiologies. Although genetic contributions are recognized, causative variants remain insufficiently defined, and the clinical implications of extended genetic testing on ...
I. Bedei   +9 more
wiley   +1 more source

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