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Background: Calciphylaxis is a life threatening complication in renal patients. Of great importance is the identification of concomitant factors for calciphylaxis. Due to the variability of clinical presentation the evaluation of such factors may be obscured when calciphylaxis diagnosis is based just on clinical features. We aimed to characterize associated factors only in patients with calciphylaxis proven by histomorphological parameters in addition to clinical presentation.
Methods: In a single center retrospective study we analyzed 15 patients in an 8 year period from 2008 to 2016. Only patients with clinical features and histomorphological proof of calciphylaxis were included. Criteria for histological diagnosis of calciphylaxis were intimal hyperplasia, micro thrombi or von Kossa stain positive media calcification.
Results: The mean age of patients was 64.8 years. Nine patients (60%) were female; 12 (80%) were obese with a Body-Mass-Index (BMI) > 30 kg/m; 3 (20%) had no renal disease; 12 (80%) had CKD 4 or 5 and 10 (66.7%) had end-stage renal disease (ESRD). One-year mortality in the entire cohort was 73.3%. With respect to medication history, the majority of patients (n = 13 (86.7%)) received vitamin K antagonists (VKA); 10 (66.7%) were treated with vitamin D; 6 (40%) had oral calcium supplementation; 5 (33.3%) had been treated with corticosteroids; 12 (80%) were on proton pump inhibitors (PPI); 13 (86.7%) patients had a clinical proven hyperparathyroidism. Ten (66.7%) patients presented with hypoalbuminemia at diagnosis.
Conclusions: The evaluation of biopsy proven calciphylaxis demonstrates that especially treatment with vitamin K antagonists and liver dysfunction are most important concomitant factors in development of calciphylaxis. As progression and development of calciphylaxis are chronic rather than acute processes, early use of DOACs instead of VKA might be beneficial and reduce the incidence of calciphylaxis.
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http://dx.doi.org/10.1186/s12882-019-1301-6 | DOI Listing |
Ital J Dermatol Venerol
August 2025
Section of Dermatology, Department of Medical Sciences, University of Turin, Turin, Italy.
Indian J Nephrol
April 2025
Department of Nephrology, Sher-I Kashmir Institute of Medical Sciences, Srinagar, Jammu Kashmir, India.
Medicina (B Aires)
August 2025
Unidad de Dermatología, Hospital de Infecciosas Francisco J. Muñiz, Buenos Aires, Argentina.
Calciphylaxis is a rare, highly mortal disease, typically diagnosed in patients with end-stage renal disease. This disorder usually presents as necrotic ulcers in acral or adipose areas. Penile necrosis due to calciphylaxis is an uncommon condition with a poor prognosis.
View Article and Find Full Text PDFJ Surg Res
August 2025
Department of Endocrine Surgery, Cleveland Clinic Foundation, Cleveland, Ohio; Cleveland Clinic Lerner College of Medicine of Case Western Reserve University, School of Medicine, Cleveland, Ohio. Electronic address:
Introduction: Calcific uremic arteriolopathy (CUA), also known as calciphylaxis, is a rare and potentially lethal condition associated with longstanding renal failure. It is defined by calcium and parathyroid hormone dysregulation, which leads to vascular calcification, painful skin necrosis, and high rates of sepsis-driven mortality. Although the mainstay treatment is medical therapy and supportive care, severe or recalcitrant cases will require parathyroidectomy, a modality associated with high perioperative complication rates of up to 40%.
View Article and Find Full Text PDFJ Educ Teach Emerg Med
July 2025
University of California, Irvine Health, Department of Emergency Medicine, Orange, CA.
Unlabelled: Calciphylaxis is a rare condition that is not well understood but is known to carry significant morbidity and mortality. We present a 44-year-old male with a history of end-stage renal disease on dialysis complaining of increasingly painful chronic wounds. The patient's physical exam was remarkable for ulcerated, bilateral anterior leg wounds with large areas of eschar along with purulent drainage.
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