نتایج جستجو برای: calcinosis

تعداد نتایج: 6088  

 Subcutaneous calcinosis consists of abnormal calcium deposition in soft tissues and is one of the complications of scleroderma, especially in limited systemic sclerosis. It is one of the criteria of CREST syndrome (calcinosis cutis, Raynaud phenomenon, esophageal dysfunction, sclerodactyly, and telangiectasia). A 44-year-old woman with systemic scleroderma for 20 years was presented with pain ...

Journal: :Annals of the rheumatic diseases 1992
E C Moore F Cohen S D Douglas V Gutta

There is a high incidence of staphylococcal infection in children with dermatomyositis, which is limited to those children who either already have or subsequently develop calcinosis. Of 15 children followed up for 3-10 years after diagnosis, all nine who developed calcinosis had infections with Staphylococcus aureus compared with none of six without calcinosis. Of these nine, the occurrence of ...

2008
J. Mark Evans Catherine C. Roberts Thomas K. Lidner

We report a case of a 75-year-old female with bilateral thigh pain for several years secondary to soft tissue calcification. Massive calcinosis of the soft tissues is a unique, but not uncommon, radiographic finding. On the contrary, tumoral calcinosis is a rare familial disease. The term tumoral calcinosis has been overly used to describe any massive collection of periarticular calcification. ...

Journal: :Reumatismo 2016
C K Tan E Suresh

Calcinosis is a well-recognized manifestation of systemic sclerosis. Paraspinal or intraspinal calcinosis is rare, with reports of calcinosis involving the cervical, thoracic and lumbar separately, but not together. We now report a case of limited cutaneous scleroderma with extensive paraspinal calcinosis of the cervical and lumbar spine.

2008
J. Mark Evans Catherine C. Roberts Thomas K. Lidner

We report a case of a 75-year-old female with bilateral thigh pain for several years secondary to soft tissue calcification. Massive calcinosis of the soft tissues is a unique, but not uncommon, radiographic finding. On the contrary, tumoral calcinosis is a rare familial disease. The term tumoral calcinosis has been overly used to describe any massive collection of periarticular calcification. ...

Journal: :Modern rheumatology 2011
Kengo Harigane Yuichi Mochida Katsushi Ishii Shigeru Ono Naoto Mitsugi Tomoyuki Saito

We report a rare case of dystrophic calcinosis in a patient with rheumatoid arthritis in bilateral buttock lesions and the right elbow joint. The calcinosis was surgically removed because it caused severe local pain, possible infection, and difficulty in sitting. Because no recommended standard pharmacotherapy exists for dystrophic calcinosis, surgical treatment should be taken into considerati...

Journal: :Journal of radiology case reports 2012
Cheryl G Zvaigzne David J Patton Harmeet Kaur Cynthia L Trevenen Deepak Kaura

Tumoral calcinosis is uncommon in toddlers, and rare within the subscapular area. Although typically benign, tumoral calcinosis is often incorrectly diagnosed prior to biopsy. We present a case of subscapular tumoral calcinosis in a 16-month old girl and discuss the radiological findings on X-ray, ultrasound, computed tomography and magnetic resonance imaging, including the first description of...

Journal: :Veterinary dermatology 2011
Arnaud Muller Frédérique Degorce-Rubiales Eric Guaguère

Metastatic calcinosis associated with chronic renal failure and multiple urinary tract abnormalities was diagnosed in a 6-month-old Brittany spaniel that was presented with calcinosis cutis. This case report highlights the importance of skin as an indicator of systemic disease. The aetiopathogenesis of the four main types of tissue calcification is defined and discussed with an emphasis on meta...

2017
A. B. Orandi K. W. Baszis V. R. Dharnidharka A. M. Huber M. F. Hoeltzel

BACKGROUND There is no standardized approach to the management of JDM-associated calcinosis and its phenotypes. Current knowledge of treatment outcomes is confined to small series and case reports. We describe physician perspectives toward diagnostic approach, classification and treatment directly targeting calcinosis, independent of overall JDM therapy. METHODS An electronic survey of 22 que...

Journal: :Clinical and experimental rheumatology 2017
Micaela Fredi Francesca Bartoli Ilaria Cavazzana Angela Ceribelli Nice Carabellese Angela Tincani Minoru Satoh Franco Franceschini

OBJECTIVES We aimed to identify the possible clinical and laboratory predictors of calcinosis in a cohort of patients with a diagnosis of polymyositis (PM) and dermatomyositis (DM). METHODS We carried out a retrospective analysis of a cohort of myositis patients attending our clinic between January 2013 and May 2014. RESULTS 74 patients (58 females, 16 males) with PM (30 cases), DM (30 case...

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