Results 51 to 60 of about 33,094 (317)

Idiopathic Scrotal Calcinosis: A Case Report and Review of Postoperative Outcomes

open access: yesCase Reports in Urology, 2020
Idiopathic scrotal calcinosis is a rare condition, characterized by the idiopathic deposition of calcium in the scrotal dermis leading to the formation of a single nodule or multiple nodules of different sizes.
M. Kyei   +3 more
semanticscholar   +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

Sclerotic metaphyseal lines in children and adolescents treated with alendronate [PDF]

open access: yes, 2010
INTRODUCTION: Bisphosphonates inhibit bone resorption by interfering with the action of osteoclasts. Among the adverse effects, sclerotic lines observed in the metaphysis of long bones have been described as the main imaging finding in pediatric patients.
Barbosa, Cassia Maria Passarelli Lupoli   +5 more
core   +3 more sources

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

Cell Calcification Models and Their Implications for Medicine and Biomaterial Research

open access: yesAdvanced Healthcare Materials, EarlyView.
Calcification, is the process by which the tissues containing minerals are formed, occurring during normal physiological processes, or in pathological conditions. Here, it is aimed to give a comprehensive overview of the range of cell models available, and the approaches taken by these models, highlighting when and how methodological divergences arise,
Luke Hunter   +5 more
wiley   +1 more source

Telomere Length of Peripheral Blood Leukocytes Predicts Disease Severity and Worse Survival in Systemic Sclerosis

open access: yesArthritis &Rheumatology, EarlyView.
Objective Peripheral blood leukocyte telomere length (PBL‐TL) shortening is associated with systemic sclerosis–related interstitial lung disease (SSc‐ILD). However, its association with other organ involvement, disease severity, and survival remains unclear.
Monica M. Yang   +6 more
wiley   +1 more source

Winer’s Nodular Calcinosis Mimicking Squamous Cell Carcinoma On The Ear

open access: yesTurkish Journal of Plastic Surgery, 2017
Winer’s nodular calcinosis, presenting as an asymptomatic, firm, white, or yellow nodule at birth or during early childhood, is a form of idiopathic calcinosis cutis. Ulceration on Winer’s nodular calcinosis is rarely seen.
Emine Çiğdem Karadağ   +2 more
doaj   +1 more source

Tumoral calcinosis

open access: yesJournal of British Surgery, 1983
Abstract Tumoral calcinosis is an uncommon, usually solitary, tumour-like mass characterized by soft tissue calcification for no apparent reason. Nearly all cases have occurred in negroes, including 2 previously recorded in this country.
S A, Knowles, G, Declerck, P P, Anthony
openaire   +2 more sources

High proton pump inhibitor exposure increases risk of calcinosis in systemic sclerosis.

open access: yesRheumatology, 2020
OBJECTIVE To investigate the association between proton pump inhibitor (PPI) use and the presence and severity of calcinosis in SSc. METHODS We analysed data from two SSc cohorts from a single centre.
Lauren V Host   +5 more
semanticscholar   +1 more source

Concurrent Psoriasis and Dermatomyositis: Retrospective Analysis and Literature Review

open access: yesJEADV Clinical Practice, EarlyView.
ABSTRACT Background Psoriasis (PsO) and dermatomyositis (DM) are both autoimmune‐mediated, inflammatory conditions. The concurrence of PsO and DM is rare, and literature on their relationship remains limited. Additionally, cutaneous DM can be challenging to clinically diagnosis, often presenting with psoriasiform clinical features.
Emily R. Gordon   +5 more
wiley   +1 more source

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