Mixed Connective Tissue Disorder Associated with Scleroderma Renal Crisis
نویسندگان
چکیده
منابع مشابه
Mixed connective tissue disorder and Castleman's disease.
We present a 16-year-old girl who presented with polyarthritis in association with Raynaud's phenomenon, malar rash, oral ulcers, photosensitivity and alopecia of 6 months duration. On evaluation, it emerged that she had a mixed connective tissue disorder with a mesangio-proliferative glomerulonephritis. Her Chest radiograph revealed a well defined left mid and lower zone opacity with evidence ...
متن کاملScleroderma Renal Crisis
Scleroderma renal crisis (SRC) is an infrequent complication of a rare disease. To date, many aspects of the pathophysiology of SRC are still mysterious. Since SRC biopsies are not frequently encountered in practice, our understanding of the spectrum of histologic changes is derived from a combination of a limited personal experience and data obtained from several relatively small pathologic st...
متن کاملIntriguing presentation of scleroderma renal crisis (scleroderma renal crisis sine scleroderma sine hypertension).
Key words: systemic sclerosis; scleroderma renal crisis; to complain of arthralgia affecting mainly her wrists sine scleroderma; sine hypertension and small joints of the hands. For the last several months she had experienced difficulty in swallowing and anorexia with a resultant weight loss of 20 kg. Despite these symptoms, she did not seek medical
متن کاملRenal complications and scleroderma renal crisis.
Scleroderma renal crisis (SRC) occurs in 5-10% of SSc patients, who may present with an abrupt onset of hypertension, acute renal failure, headaches, fevers, malaise, hypertensive retinopathy, encephalopathy and pulmonary oedema. Patients at greatest risk of developing SRC are those with diffuse cutaneous or rapidly progressive forms of SSc, and treatment with a recently commenced high dose of ...
متن کاملMixed connective tissue disease with associated glomerulonephritis and hypocomplementaemia.
Mixed connective tissue disease is an increasingly recognized entity in which renal disease is thought to be unusual and associated hypocomplementaemia even more uncommon. A patient is described who had both these features and who also illustrates many of the characteristic features of this syndrome. The response to steroids of the systemic sclerosis component is well shown and an additional fe...
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ژورنال
عنوان ژورنال: Journal of Nephrology & Therapeutics
سال: 2014
ISSN: 2161-0959
DOI: 10.4172/2161-0959.1000154