Results 41 to 50 of about 15,703 (219)

Familial tumoral calcinosis [PDF]

open access: yes, 2014
Introduction: Tumoral calcinosis is a rare condition characterised by progressive, ectopic, periarticular deposits of calcium. These tumour-like growths often infiltrate muscle and tendon, usually presenting as multiple masses or as a painless, solitary ...
Alkhatib, Amal   +2 more
core   +1 more source

Calcinosis cutis arising in morphea: a case series [PDF]

open access: yes, 2020
Calcinosis cutis, although common in systemic sclerosis, has been rarely reported in patients with morphea. We describe four patients with calcinosis cutis arising within morphea plaques, discuss their treatments and outcomes, and review previously ...
Brockman, R   +4 more
core   +1 more source

Osteoclastogenesis in Patients With Systemic Sclerosis With and Without Calcinosis Cutis

open access: yesACR Open Rheumatology
Objective We aimed to assess whether the presence of radiographically confirmed calcinosis of the hands in patients with systemic sclerosis (SSc) is associated with increased osteoclastogenesis.
Antonia Valenzuela   +6 more
doaj   +1 more source

Iatrogenic calcinosis cutis in 9-month-old baby boy: a case report

open access: yesJournal of Medical Case Reports, 2022
Background Calcinosis cutis is a rare condition, characterized by an accumulation of calcium salts in the skin and subcutaneous tissue. There are several types of this condition, including dystrophic, metastatic, idiopathic, calciphylaxis, and iatrogenic
Eman Ahmed Alghaith   +2 more
doaj   +1 more source

Characteristics and Outcomes of Male Participants in a Multicenter Longitudinal Australian Study Cohort

open access: yesArthritis Care &Research, EarlyView.
Objective The aim of this study was to determine the differences in demographic, serologic, and clinical characteristics between male and female patients with systemic sclerosis (SSc) in an Australian cohort. Methods This was a retrospective observational study using data from the Australian Scleroderma Cohort Study.
Emily Lin   +14 more
wiley   +1 more source

Tumoral calcinosis

open access: yesJournal of British Surgery, 1972
Abstract An extreme case of tumoral calcinosis is presented. This condition is common in the highland natives of New Guinea and is commonly referred to as “hip stones”. The pathogenesis, clinical findings, and treatment are discussed and the relevant literature is reviewed.
openaire   +2 more sources

Subcutaneous calcinosis: Is it different between systemic sclerosis and dermatomyositis? [PDF]

open access: yes, 2021
Calcinosis cutis is the deposition of insoluble calcium in the skin and subcutaneous tissues. It is a manifestation of several autoimmune connective tissue diseases, most frequently with systemic sclerosis and juvenile dermatomyositis, followed by adult ...
Valenzuela Vergara, Antonia María   +1 more
core   +1 more source

Artificial Intelligence in Systemic Sclerosis: Clinical Applications, Challenges, and Future Directions

open access: yesArthritis Care &Research, EarlyView.
Systemic sclerosis (SSc) is a rare autoimmune disease defined by immune dysregulation, vasculopathy, and progressive fibrosis of the skin and internal organs. Despite advances in care, major complications such as interstitial lung disease (ILD) and myocardial involvement remain the leading causes of morbidity and mortality.
Cristiana Sieiro Santos   +2 more
wiley   +1 more source

Idiopathic scrotal calcinosis [PDF]

open access: yes, 2002
The appearance of calcific masses within the dermis of scrotal skin is generally referred to as idiopathic scrotal calcinosis. Some authors suggest that the lesions result from dystrophic calcification of epidermal cysts.
Nazir, Salmy
core  

PRIMARY NORMO-PHOSPHATEMIC TUMORAL CALCINOSIS - A RARE ENTITY [PDF]

open access: yes, 2022
Tumoral calcinosis is a rare benign condition, characterized by massive deposition of calcium salts into peri-articular soft tissues. Majority are secondary to underlying chronic disorders like chronic renal failure.
Shashi Ranjan   +3 more
core   +1 more source

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