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Penile and digital calciphylaxis: A case report and literature review
Insights
Calcific uremic arteriolopathy (CUA) is a severe condition causing tissue death. Early diagnosis and treatment, including managing mineral metabolism, are crucial for improving outcomes in hemodialysis patients.
Area of Science:
- Nephrology
- Vascular Medicine
- Dermatology
Background:
- Calcific uremic arteriolopathy (CUA) is a rare vascular complication in patients with chronic kidney disease (CKD) and end-stage renal disease (ESRD).
- CUA presents with painful skin necrosis and has a high mortality rate, often associated with dysregulation of calcium and phosphate metabolism.
Approach:
- This report details a case of a 58-year-old male on hemodialysis (HD) for obstructive uropathy-induced CKD.
- The patient experienced distal penile ischemia followed by digital necrosis, diagnosed via skin biopsy confirming CUA.
- Treatment involved surgical debridement, hyperbaric oxygen, intensified HD, phosphate control, and sodium thiosulfate administration.
Key Points:
- An unusual presentation of CUA occurred in a non-diabetic, non-anticoagulated patient shortly after initiating HD.
- Severe dysregulation of calcium and phosphate metabolism was a key factor.
- Successful management involved a multi-modal approach including intensified HD and sodium thiosulfate.
Conclusions:
- This case highlights the importance of recognizing CUA in hemodialysis patients, even with atypical initial presentations.
- Aggressive management of mineral and bone disorder is critical for CUA treatment.
- Sodium thiosulfate shows promise as a therapeutic option for CUA.
Abstract:
Calcific uremic arteriolopathy (CUA) represents a rare but severe disease with high morbimortality. The authors present the case of a 58-year-old male patient with chronic kidney disease due to obstructive uropathy, on hemodialysis (HD). He started HD due to uremic syndrome with a severe renal dysfunction, dysregulation of calcium and phosphate metabolism, and he presented with distal penile ischemia, which was treated with surgical debridement and hyperbaric oxygen therapy. Four months later, painful distal digital necrosis of both hands was observed. Extensive arterial calcification was observed on X-ray. A skin biopsy confirmed the presence of CUA. Sodium thiosulfate was administered for 3 months, HD was intensified, and hyperphosphatemia control was achieved, with progressive improvement of the lesions. This case illustrates an uncommon presentation of CUA in a patient on HD for a few months, non-diabetic and not anticoagulated, but with a severe dysregulation of calcium and phosphate metabolism.
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