Results 71 to 80 of about 15,703 (219)

Telangiectasia in Systemic Sclerosis Is a Marker of Increased Disease Morbidity and Mortality: Analyses From the Australian Scleroderma Cohort Study

Australasian Journal of Dermatology, EarlyView.
ABSTRACT This Australian retrospective cohort analysis of 1977 patients investigates and expands on correlates of telangiectasia in systemic sclerosis to determine whether this cutaneous sign is a potential surrogate marker for disease progression and prognosis.
Vivien Wai Yun Lai, Dylan Hansen, Maryam Tabesh, Jessica Fairley, Laura Ross, Nava Ferdowsi, Gene‐Siew Ngian, Diane Apostolopoulos, Joanne Sahhar, Lauren V. Host, Jennifer Walker, Gabor Major, Susanna Proudman, Wendy Stevens, Mandana Nikpour, Amanda M. Saracino   +15 more
wiley   +1 more source

Calcinosis in systemic sclerosis: prevalence, clinical picture, management, complications

Bolʹ, Sustavy, Pozvonočnik, 2019
This literature review summarizes current data on the epi­demiology, pathophysiology, diagnosis and treatment of calcinosis cutis in patients with systemic sclerosis (SSc).
Ye.D. Yehudina, I.Yu. Golovach
doaj   +1 more source

Extensive Tumoral Calcinosis of the Hand. [PDF]

, 2021
Tumoral calcinosis is a rare and benign subtype of calcinosis cutis, a group of disorders involving soft tissue calcium deposition. Only 250 cases have been described since 1898; hand involvement is exceedingly rare.
Ayalon, Omri, Gonzalez, Matthew, MD, Rettig, Michael   +2 more
core  

Histopathologic Characterization of Cutaneous Oxalosis Mimicking Calciphylaxis: Diagnostic Pitfalls and Polarized Light Evaluation

Journal of Cutaneous Pathology, EarlyView.
ABSTRACT Cutaneous oxalosis is an uncommon manifestation of primary hyperoxalosis, which can often resemble other cutaneous manifestations of end stage renal disease (ESRD), particularly calciphylaxis. We report the case of a 46 year old female with primary hyperoxaluria type one (PH1) believed to be well‐controlled on lumasiran, a small interfering ...
Shrina Patel, Brad Graham, Kaci Reaves, Mya Phelps   +3 more
wiley   +1 more source

Idiopathic Calcinosis Cutis over Elbow in a 12-Year Old Child

Case Reports in Orthopedics, 2013
Calcinosis cutis is an uncommon disorder caused by an abnormal deposit of calcium phosphate in the skin in various parts of the body. Four main types of calcinosis cutis have been recognized according to etiology: associated with localized or widespread ...
S. K. Venkatesh Gupta, Ramana Rao Balaga, Suman Kumar Banik   +2 more
doaj   +1 more source

Assessment, classification and treatment of calcinosis as a complication of juvenile dermatomyositis: a survey of pediatric rheumatologists by the childhood arthritis and rheumatology research alliance (CARRA)

Pediatric Rheumatology Online Journal, 2017
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.
A. B. Orandi, K. W. Baszis, V. R. Dharnidharka, A. M. Huber, M. F. Hoeltzel, for the CARRA Juvenile Myositis subgroup   +5 more
doaj   +1 more source

Dental findings of hyperphosphatemic familial tumoral calcinosis [PDF]

, 2017
Tumoral calcinosis is a rare familial disorder characterized by masses of calcification in periarticular soft tissues. Few reports in the literature have described dental abnormalities in patients with tumoral calcinosis.
TATAR, İLKAN, ÇELİK, HAKAN HAMDİ, Ozbek, Murat, AKKAYA, NURSEL, YILANCI, Humeyra Ozge   +4 more
core   +1 more source

Clinical course and potential associated factors of progressive calcinosis cutis in early systemic sclerosis: a cohort study

Annals of Medicine
Background Calcinosis cutis of hands can progress and impair hand function in systemic sclerosis (SSc). Understanding the natural disease and comprehensive management is crucial.Objective To examine clinical course and identify risk factors associated ...
Vassana Kanjanajarurat, Prathana Chowchuen, Chingching Foocharoen, Punthip Thammaroj   +3 more
doaj   +1 more source

Multiple External Invasive Root Resorption and Calcification in Systemic Sclerosis—Case Report

International Endodontic Journal, EarlyView.
ABSTRACT Aim There are few reports in the literature of multiple external invasive root resorption (EIRR) lesions in patients with systemic sclerosis (SSc), and an association between root resorption and SSc is not well established. We report the only case that comprehensively illustrates—with the combination of histopathology, cone beam computed ...
Jee‐Yun Leung, Geoffrey Heithersay, Richard Logan, Sharon Liberali   +3 more
wiley   +1 more source

Abatacept in the Treatment of Juvenile Dermatomyositis-Associated Calcifications in a 16-Year-Old Girl

Case Reports in Rheumatology, 2020
Calcinosis is a feared complication of JDM that may be seen in up to 40% of children with JDM. It is associated with negative impact on the patients’ quality of life due to weakness, functional disability, joint contractures, muscle atrophy, skin ulcers,
Sukesh Sukumaran, Vini Vijayan
doaj   +1 more source