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Published on: July 19, 2018
[Systemic calciphylaxis and acquired perforating disease in a uremic patient]
M J Asensio Sánchez1, L J Del Pozo Hernando, A Martínez Díaz
1Servicio de Nefrología, Hospital del INSALUD de Soria.
Insights
A hemodialysis patient with chronic renal failure developed rapidly progressive ischemic necrosis in extremities, requiring amputation. New lesions appeared after parathyroidectomy, suggesting a link between acquired perforating disease and calciphylaxis in uremia.
Area of Science:
- Nephrology
- Dermatology
- Vascular Medicine
Background:
- Chronic renal failure (CRF) patients on hemodialysis often experience complications.
- Vascular calcification and secondary hyperparathyroidism are common in CRF.
Observation:
- A patient with CRF on hemodialysis presented with rapidly progressive ischemic necrosis of digits.
- Radiological and pathological findings revealed diffuse vascular calcifications.
- Elevated parathyroid hormone (PTH) and phosphocalcic product were noted.
Findings:
- Amputation was necessary due to ischemic necrosis.
- Following parathyroidectomy, initial improvement was followed by new ischemic lesions and keratotic papules on the buttocks and lower extremities.
- Histological examination showed perforation of these new lesions, leading to necrosis.
Implications:
- This case highlights the potential coexistence of acquired perforating disease and calciphylaxis in uremic patients.
- The findings suggest a complex interplay between mineral metabolism, vascular health, and skin manifestations in advanced kidney disease.
- Further research is warranted to understand and manage these severe complications in hemodialysis patients.
Abstract:
We show the case of a patient suffering from a chronic renal failure in hemodialysis. He had a ischemic necrosis that was quickly progressive in his fingers and toes. It was necessary to amputate them. Diffuse vascular calcifications were recorded so radiologically than pathologically. PTH and phosphocalcic product were raised. Parathyroidectomy was practised with a quick initial improvement but immediately new distal ischemic lesions and keratotic papules with histologic perforation, that became necrosed, appeared in his buttocks and inferior extremities. The coexistence of acquired perforating disease and calciphylaxis in uremic patients has not been reported until now.
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