Radiographic Features of Rhupus Arthropathy
نویسندگان
چکیده
منابع مشابه
Rhupus arthropathy in childhood-onset systemic lupus erythematosus
Case report A 13-year-old female presented to our hospital for the first time with complaints of pain in joints, which had been present for 3 years. Initially, the patient had pain in the knee joints. Later, the wrist and small joints of the hands were also involved. The patient complained of stiffness and limitation of mobility around all affected joints and she suffered worsening symptoms for...
متن کاملDeforming arthropathy or lupus and rhupus hands in systemic lupus erythematosus.
OBJECTIVE Although deforming arthropathy in systemic lupus erythematosus (SLE) is characterised by a number of manifestations, definitive criteria for the different forms have not yet been established. To define deforming arthropathy and its different types a study was undertaken of 176 SLE patients. METHODS Using as criterion any deviation from any of the metacarpus finger axes 17 patients (...
متن کاملRhupus arthropathy as the presenting manifestation in Juvenile SLE: a case report
An 8.5-year-old girl was referred with swelling of both knees lasting for two years. ANA was found as negative. She was diagnosed as oligoarticular JIA. After two years of follow-up, thrombocytopenia was detected during routine screening. Her ANA and anti ds-DNA antibodies also became positive, with low levels of C3 and C4. She was diagnosed as Juvenile SLE, meeting the criteria cytopenia, posi...
متن کاملClinical and radiological features of down's arthropathy
Introduction The ‘Arthropathy of Down syndrome’ was first described in 1984. Three decades on we still have limited literature on the clinical and radiological features of this arthritis, despite the fact that it is thought to be 3-6 times more common than JIA in the general paediatric population. Down’s Arthropathy (DA) is rarely recognised at onset, and remains under-diagnosed and largely und...
متن کاملRadiographic features of osteogenesis imperfecta
BACKGROUND Osteogenesis imperfecta (OI), commonly called "brittle bone disease", is a genetic disorder characterised by increased bone fragility and decreased bone density due to quantitative and/or qualitative abnormalities of type I collagen. Different types of OI exist, from mild to severe; they may lead to death, multiple bone fractures, skeletal deformity and short stature. METHODS Sever...
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ژورنال
عنوان ژورنال: Internal Medicine
سال: 2013
ISSN: 0918-2918,1349-7235
DOI: 10.2169/internalmedicine.52.1454