Results 1 to 10 of about 29,117 (272)

Is Anti-NXP2 Autoantibody a Risk Factor for Calcinosis and Poor Outcome in Juvenile Dermatomyositis Patients? Case Series

Frontiers in Pediatrics, 2022
Juvenile dermatomyositis (JDM) has a wide spectrum of clinical presentations. In the last decade, several myositis-specific antibodies have been identified in patients with JDM and connected with specific organ involvement or specific clinical picture ...
Natasa Toplak, Pallavi Pimpale Chavan, Silvia Rosina, Tomas Dallos, Oz Rotem Semo, Cassyanne L. Aguiar, Raju Khubchandani, Angelo Ravelli, Angelo Ravelli, Anjali Patwardhan   +9 more
doaj   +2 more sources

Calcinosis in juvenile dermatomyositis: Updates on pathogenesis and treatment

Frontiers in Medicine, 2023
Calcinosis, or the deposition of insoluble calcium salts in the skin, subcutaneous tissue, fascia, tendons, and muscles, is a feared complication of juvenile dermatomyositis.
Caitlan S. Pinotti, Laura Cannon, Jeffrey A. Dvergsten, Eveline Y. Wu, Eveline Y. Wu   +4 more
doaj   +2 more sources

Reliability of durometry to assess firmness of calcinosis lesions in Juvenile and adult dermatomyositis. [PDF]

PLoS ONE
Background/objectiveDermatomyositis (DM) and juvenile dermatomyositis (JDM) are inflammatory myopathies affecting multiple organs, including muscle and skin.
Meghan Corrigan Nelson, Lisa G Rider, Hanna Kim, Scott Gillespie, Vy Do, Julie Fuller, Kelly Rouster-Stevens, Adam Schiffenbauer   +7 more
doaj   +2 more sources

Idiopathic Penile Calcinosis Cutis: A Histopathological Case Report [PDF]

Reports
Background and Clinical Significance: Calcinosis cutis is a rare condition that can develop through several mechanisms. These include dystrophic, calciphylaxis (classical, metastatic, and iatrogenic), and idiopathic mechanisms.
George Stoyanov, Dobri Marchev, Hristo Popov   +2 more
doaj   +2 more sources

Normophosphatemic type tumoral calcinosis associated with chronic recurrent multifocal osteomyelitis: a case report

Acta Orthopaedica et Traumatologica Turcica, 2020
Chronic recurrent multifocal osteomyelitis (CRMO) and tumoral calcinosis are two distinct musculoskeletal diseases with unclear etiopathogenesis. Previously, two CRMO cases with associated tumoral calcinosis were reported.
Halil Yalcin Yuksel, Serdar Yilmaz, Mihriban Gurbuzel   +2 more
doaj   +1 more source

Calcinosis in a roe deer fawn (Capreolus capreolus) in northern Germany

BMC Veterinary Research, 2020
Background Calcinosis has been reported for a broad range of different animals. Causes for calcinosis include metabolic disorders due to kidney failure, intoxication with calcinogenic plants, or iatrogenic overdose of vitamin D.
Matthias Gerhard Wagener, Annika Lehmbecker, Melanie Bühler, Mirja Wilkens, Teresa Punsmann, Martin Ganter   +5 more
doaj   +1 more source

Clinical phenotypes and biologic treatment use in juvenile dermatomyositis-associated calcinosis [PDF]

, 2018
Background Few risk factors have been identified for the development of calcinosis among patients with Juvenile Dermatomyositis, and currently no clinical phenotype has been associated with its development.
Al-Hammadi, Noor, Baszis, Kevin W, CARRA Legacy Registry Investigators,, Dharnidharka, Vikas R, Orandi, Amir B   +4 more
core   +2 more sources

Cervical and lumbar paraspinal calcinosis in systemic sclerosis

Reumatismo, 2016
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.
C.K. Tan, E. Suresh
doaj   +1 more source

Hyperphosphatemic familial tumoral calcinosis mimicking a cystic hemo-lymphangioma on MRI

Radiology Case Reports, 2022
A tumoral calcinosis is a rare benign pathology characterized by calcium deposits (calcium phosphate crystals) in the periarticular soft tissues, giving a truly pseudotumor appearance.
Salma El Houss, MD, Najlae LRhorfi, PhD, Zakia El Yousfi, MD, Siham EL Haddad, PhD, Latifa Chat, PhD, Nazik Allali, PhD, Naji Rguieg, MD, Najat Lamalmi, PhD   +7 more
doaj   +1 more source

Autoimmune hyperphosphatemic tumoral calcinosis in a patient with FGF23 autoantibodies [PDF]

, 2018
Hyperphosphatemic familial tumoral calcinosis (HFTC)/hyperostosis-hyperphosphatemia syndrome (HHS) is an autosomal recessive disorder of ectopic calcification due to deficiency of or resistance to intact fibroblast growth factor 23 (iFGF23). Inactivating
Burbelo, Christopher J. Romero, Daniela Egli-Spichtig, Emily Farrow, Farzana Perwad, Ichikawa, Lori C. Guthrie, Mary Scott Roberts, Michael J. Econs, Michael T. Collins, Peter D. Burbelo, Rachel I. Gafni, Shimada, Shoji Ichikawa, Uchida   +14 more
core   +1 more source