Results 61 to 70 of about 18,009 (224)
Rheumatology &Autoimmunity, EarlyView.Summary of pregnancy management in CTD‐ILD across preconception, antenatal, and postpartum phases, emphasizing risk stratification and multidisciplinary care. 6MWT, 6‐min walk test; CTD‐ILD: connective tissue disease‐interstitial lung disease; DLCO, diffusion capacity of the lung for carbon monoxide; FVC, forced vital capacity; MDT, multidisciplinary ...
Khaled Aldhuaina +3 more
wiley +1 more source
Journal of Cutaneous Pathology, EarlyView.ABSTRACT Squamoid Eccrine Ductal Carcinoma (SEDC) is a rare cutaneous adenexal carcinoma first described in 1997. It has distinct biphasic features on histology which commonly result in misdiagnosis as Bowen disease or cutaneous squamous cell carcinomas (cSCC) if diagnostic skin biopsies are too superficial. This may lead to a delay in diagnosis. It is
Xiang Li Tan +15 more
wiley +1 more source
Polyomyositis and myocarditis associated with acquired toxoplasmosis in an immunocompetent girl
BMC Musculoskeletal Disorders, 2001 Background Acquired toxoplasmosis more frequently goes unrecognized. Immunocompetent adults and adolescents with primary infection are generally asymptomatic, but symptoms may include malaise, fever, and lymphadenopathy.
Tsagkaraki Daria +4 more
doaj +1 more source
European Journal of Haematology, EarlyView.ABSTRACT Eosinophilia, defined as an absolute eosinophil count (AEC) of ≥ 0.5 × 109/L, is a frequently encountered finding with a vast spectrum of potential underlying etiologies. Hypereosinophilia (HE) is defined as AEC > 1.5 × 109/L and may become life‐threatening when eosinophil‐induced organ damage occurs, defining the hypereosinophilic syndrome ...
Stijn Wigerinck, Peter Vandenberghe
wiley +1 more source
Polymyositis as a cause of total gut failure
, 2002 BACKGROUND: Gastrointestinal manifestations are seen in systemic sclerosis and mixed connective tissue disorders but are rare in pure polymyositis. CASE REPORT: A 44 year old woman with polymyositis who developed total gut failure requiring treatment ...
Rankin, Elizabeth +3 more
core +1 more source
Idiopathic inflammatory myopathies: Contributions from India
Indian Journal of Rheumatology, 2020 A careful literature search would reveal significant contributions by Indian clinicians and basic researchers in the field of Idiopathic inflammatory myopathies (IIMs).
Anand Narayan Malaviya
doaj +1 more source
Occurrence of infections in dogs receiving ciclosporin in a single‐centre UK referral population
Journal of Small Animal Practice, EarlyView.Objectives The study aimed (a) to describe the occurrence and nature of new infections in dogs receiving oral ciclosporin and (b) to identify any risk factors associated with the development of a new infection whilst receiving ciclosporin. Materials and Methods In this retrospective cohort study, medical records of dogs presented to a private UK ...
S. Dormon +5 more
wiley +1 more source
Dermatomyositis, polymyositis and immune-mediated necrotising myopathies [PDF]
, 2015 Dermatomyositis, polymyositis and immune-mediated necrotising myopathy are major forms of idiopathic inflammatory myopathy. We review here recent developments in understanding the pathology and pathogenesis of these diseases, and characterisation of ...
Mastaglia, F.L. +5 more
core +1 more source
Arquivos de Neuro-Psiquiatria, 1976 An electrophysiological study has been made of the extensor digitorum brevis, thenar and hypothenar muscles in 25 patients with chronic and acute polymyositis.
R. E. P. Sica +3 more
doaj
Primary Sjögren’s syndrome with polymyositis, a rare amalgamation
Egyptian Rheumatology and Rehabilitation, 2018 Sjögren’s syndrome is characterized by diminished lacrimal and salivary gland secretory function. This disorder is not strictly confined to the exocrine glands and its manifestations may extend to extraglandular sites, such as the lungs, kidneys ...
Harpreet Singh +3 more
doaj +1 more source