Results 51 to 60 of about 1,960 (186)

Metastatic calcinosis cutis in a dialysis patient

, 2023
Metastatic calcinosis cutis is an uncommon complication of end-stage kidney disease but has severe and disabling effects. Its development is attributed to disorders of calcium and phosphate metabolism associated with secondary hyperparathyroidism.
Bapoo, Nabeel, Stead, Piers A, Ally, Ismail, Chothia, Mogamat-Yazied   +3 more
core   +1 more source

Real‐World Safety and Effectiveness of JAK Inhibitors in Systemic Sclerosis: A Propensity‐Matched Study from the EUSTAR Cohort

Arthritis Care &Research, Accepted Article.
Objective JAK inhibitors (JAKis) have shown promising effects in early‐phase studies of SSc. We aimed to assess the safety and explore effectiveness of JAKis compared to conventional immunosuppressants in SSc. Methods A longitudinal retrospective study of the EUSTAR cohort was performed.
Stefano Di Donato, Marie‐Elise Truchetet, Marco Minerba, Oliver Distler, Juan José Alegre Sancho, Yolanda Braun‐Moscovici, Christina Bergmann, Petros Sfikakis, Jeska K de Vries‐Bouwstra, Murray Baron, Silvia Bellando‐Randone, Lorenzo Dagna, Christopher P Denton, Madelon C Vonk, Vanessa Smith, Ivan Castellvi, Gabriela Riemekasten, Andra Balanescu, Masataka Kuwana, Maria De Santis, Kamal Solanki, Anastas Batalov, Vahan Mukuchyan, Marco Matucci‐Cerinic, Yannick Allanore, Francesco Del Galdo, Michael Hughes, EUSTAR Collaborators   +27 more
wiley   +1 more source

Calcinosis Cutis and Delayed‐Onset Myositis in a Case of Suspected Localized Scleroderma: A Diagnostic and Therapeutic Challenge

Pediatric Dermatology, EarlyView.
ABSTRACT A 16‐year‐old girl presenting with calcinosis cutis and localized scleroderma subsequently developed delayed‐onset idiopathic inflammatory myopathy five years after initial skin involvement. Despite the absence of typical dermatomyositis features and negative myositis‐specific antibodies, whole‐body MRI revealed extensive subclinical muscle ...
Edoardo Marrani, Laura Gatti, Ilaria Pagnini, Teresa Oranges, Cesare Filippeschi, Gabriele Simonini   +5 more
wiley   +1 more source

Constitutional symptoms and response to Penicillin G in erysipelas and cellulitis – a monocentric, retrospective, explorative study

JDDG: Journal der Deutschen Dermatologischen Gesellschaft, Volume 24, Issue 6, Page 746-754, June 2026.
Summary Background: Erysipelas, caused by streptococci, should be treated with penicillin, while uncomplicated cellulitis (phlegmon), often caused by Staphylococcus aureus, requires penicillinase‐resistant beta‐lactam antibiotics, which have a higher risk of adverse effects. Distinguishing between these infections is important.
Helena Schieffers, Cord Sunderkötter
wiley   +1 more source

Epidemiology and treatment of calcinosis cutis: 13 years of experience

Indian Journal of Dermatology, 2020
Background: Calcinosis cutis is a rare condition associated with different diseases, which is difficult to manage. Aims and Objectives: In this retrospective study, the epidemiology of calcinosis cutis and the effectiveness of various treatment regimens ...
Lili Róbert, Norbert Kiss, Márta Medvecz, Enikő Kuroli, Miklós Sárdy, Bernadett Hidvégi   +5 more
doaj   +1 more source

Allgemeinsymptome und Ansprechen auf Benzylpenicillin bei Erysipel und unkomplizierter Phlegmone – eine monozentrische, retrospektive, explorative Studie

JDDG: Journal der Deutschen Dermatologischen Gesellschaft, Volume 24, Issue 6, Page 746-754, June 2026.
Zusammenfassung Hintergrund Erysipele gelten als durch Streptokokken verursachte Infektionen und sollen daher mit Penicillin behandelt werden, während Phlegmonen meist durch Staphylococcus aureus hervorgerufen werden und Penicillinase‐feste Betalaktamantibiotika benötigen. Letztere bergen ein höheres Risiko für unerwünschte Wirkungen.
Helena Schieffers, Cord Sunderkötter
wiley   +1 more source

Immune cells composition in the skin and subcutaneous adipose tissue of patients with systemic sclerosis

JDDG: Journal der Deutschen Dermatologischen Gesellschaft, Volume 24, Issue 4, Page 482-492, April 2026.
Summary Background and objectives Systemic sclerosis (SSc) is a rare, chronic autoimmune disease characterized by fibrosis of the skin and/or internal organs. Emerging evidence suggests that subcutaneous adipose tissue may contribute to systemic inflammation and fibrosis in SSc.
Marija Geroldinger‐Simić, Ana E. Aguilar González, Gerald Exler, Georg Stary   +3 more
wiley   +1 more source

Zusammensetzung der Immunzellen in der Haut und dem subkutanen Fettgewebe von Patienten mit systemischer Sklerose

JDDG: Journal der Deutschen Dermatologischen Gesellschaft, Volume 24, Issue 4, Page 482-493, April 2026.
Zusammenfassung Hintergrund und Ziele Systemische Sklerose (SSc) ist eine seltene, chronische Autoimmunerkrankung, die durch Fibrose der Haut und/oder der inneren Organe gekennzeichnet ist. Neue Erkenntnisse deuten darauf hin, dass subkutanes Fettgewebe zur systemischen Entzündung und Fibrose bei SSc beitragen kann.
Marija Geroldinger‐Simić, Ana E. Aguilar González, Gerald Exler, Georg Stary   +3 more
wiley   +1 more source

MR imaging findings of calcinosis cutis in primary Sjogren syndrome, a rare manifestation

Radiology Case Reports, 2020
Soft tissue calcifications associated with various connective tissue diseases such as dermatomyositis and scleroderma have been well documented Plaque-like sheets of subcutaneous calcifications presenting as an indurated soft tissue mass in a patient ...
Paul L. Wasserman, DO, MHCM, Carissa Wiesler, MD, Chandana Kurra, MD, Reeba Omman, MD, Kristin Taylor, MD, Ruchir Puri, MD   +5 more
doaj   +1 more source

Calcinosis Cutis Associated with Chronic Sclerodermoid Graft versus Host Disease: A Case and Review of the Literature

Case Reports in Dermatological Medicine, 2020
We present a rare case of calcinosis cutis associated with chronic sclerodermoid graft versus host disease in a 59-year-old male, 13 years following allogenic bone marrow transplantation.
Jacqueline Deen, Lisa Byrom, Ivan Robertson   +2 more
doaj   +1 more source