Results 31 to 40 of about 4,864,129 (252)

Case Report of a Female Patient with Adult-onset Still's Disease and Review of the Literature [PDF]

open access: yesIranian Journal of Immunology, 2022
Background: Adult-onset Still's disease (AOSD), which presents many non-specific symptoms, such as rash leukocytosis, spiking fever, and sore throat, is a rare auto inflammatory disease.
Yan Gao   +4 more
doaj   +1 more source

Acute Myocarditis Revealing Adult-Onset Still’s Disease

open access: yes, 2021
International audienceA 34-year-old man presented with fever, palpitations, maculopapular rash, pharyngitis, left cheilitis, and bilateral gonalgia. High-sensitivity troponin I concentration was 4,900 ng/l.
Ederhy, Stéphane   +8 more
core   +1 more source

Suppurative necrotizing granulomatous lymphadenitis in adult-onset Still’s disease: a case report

open access: yesJournal of Medical Case Reports, 2012
Introduction Lymphadenopathy is found in about 65% of patients with adult-onset Still’s disease and is histologically characterized by an intense, paracortical immunoblastic hyperplasia. Adult-onset Still’s disease has not been previously described as an
Assimakopoulos Stelios F   +5 more
doaj   +1 more source

Hemophagocytic syndrome, a rare variant of Still’s disease [PDF]

open access: yes, 2017
Adult onset still’s disease is a rare systemic inflammatory disorder of unknown etiology that is responsible for a significant number of cases of fever of unknown origin (FUO) and musculoskeletal diseases.
Dinesh Gupta   +5 more
core   +1 more source

Non-Hodgkin's lymphoma in a woman with adult-onset Still's disease: a case report

open access: yesJournal of Medical Case Reports, 2008
Introduction Adult onset Still's disease is a chronic multisystemic inflammatory disorder characterized by high spiking fever, polyarthralgia and rash.
Otrock Zaher K   +5 more
doaj   +1 more source

Adult-onset Still’s disease with prominent polyserositis

open access: yes, 2018
Adult-onset Still’s disease is a systemic autoinflammatory disease the presentation of which can often mimic infection. As a consequence, there is often a delay in diagnosis.
Ali Sibtain Farooq Sheikh   +2 more
core   +1 more source

ЛИХОРАДКА НЕЯСНОГО ГЕНЕЗА: «ПО НАПРАВЛЕНИЮ К СТИЛЛУ»

open access: yesАрхивъ внутренней медицины, 2014
The article provides the basic criteria of the clinical situation known as «fever of unknown origin» which is an interdisciplinary clinical problem. The main reasons for fever of unknown origin are infectious-inflammatory processes, malignant tumors, non-
Л. И. Дворецкий
doaj   +1 more source

A case of adult‐onset Still's disease in a patient after a car accident

open access: yesClinical Case Reports, 2023
Key Clinical Message Adult‐onset Still's disease is a rare inflammatory condition with diverse clinical features. Yamaguchi criteria aid diagnosis, and pleural effusion and elevated ferritin levels are important markers.
Feride Yaman, Ali Kimiaei
doaj   +1 more source

The diagnostic challenge of Adult-onset Still’s disease [PDF]

open access: yes, 2018
Adult-onset Still’s disease (AOSD) is a rare systemic inflammatory disease of unknown etiology, characterized by symptoms including high fever, salmon-pink rash, and also inflammatory symptoms such as sore throat, arthritis or arthralgia and ...
Rostamipour, H.A., Rastegarian, L
core   +1 more source

European Standard Clinical Practice Guideline and EXPeRT Recommendations for the Diagnosis and Management of Gastroenteropancreatic Neuroendocrine Neoplasms in Children and Adolescents

open access: yesPediatric Blood &Cancer, EarlyView.
ABSTRACT Pediatric gastroenteropancreatic neuroendocrine neoplasms (GEP‐NENs) are extremely rare and clinically heterogeneous. Management has largely been extrapolated from adult practice. This European Standard Clinical Practice Guideline (ESCP), developed by the EXPeRT network in collaboration with adult NEN experts, provides (adult) evidence ...
Michaela Kuhlen   +23 more
wiley   +1 more source

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