Results 11 to 20 of about 25,410 (271)
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 +9 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 +5 more
doaj +1 more source
Dystrophic calcinosis cutis in a patient with cutaneous sarcoidosis in remission
Skin Health and Disease, 2023 A 65‐year‐old Japanese woman was referred to our department because of a 5‐month history of asymptomatic papules on the face. She was diagnosed with cutaneous sarcoidosis on the face 20 years ago.
Miyuki Yoshikawa +3 more
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 +7 more
doaj +1 more source
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 +4 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 +14 more
core +1 more source
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
South African Journal of Radiology, 2010 Objective. Uraemic tumoral calcinosis refers to metastatic calcifications that occur rarely on the extensor surfaces of joints in patients undergoing long-term haemodialysis.
F E Suleman, V Mngomezulu, N Ebrahim
doaj +1 more source
Case Reports in Nephrology, 2021 Tumoral calcinosis is a rare but debilitating condition that can affect dialysis patients. Optimal management is largely unknown. We report the clinical course, treatment, and outcome of a peritoneal dialysis (PD) patient who developed tumoral calcinosis
Ho-Kwan Sin +11 more
doaj +1 more source
Clinical and serological features of systemic sclerosis in a multicenter African American cohort: Analysis of the genome research in African American scleroderma patients clinical database. [PDF]
, 2017 Racial differences exist in the severity of systemic sclerosis (SSc). To enhance our knowledge about SSc in African Americans, we established a comprehensive clinical database from the largest multicenter cohort of African American SSc patients assembled
Boin, Francesco +28 more
core +1 more source