VasculopathyUlcer DDxICD-10 E83.59 / N18

Calciphylaxis

Calcific uraemic arteriolopathy; CUA; uraemic gangrenous syndrome

Calciphylaxis (calcific uraemic arteriolopathy) is a rare but devastating vasculopathy of the small-vessel dermal and subcutaneous arteries — most commonly in end-stage renal disease (ESRD) on dialysis, with non-uraemic variants reported. Mural calcification with intimal hyperplasia and microthrombosis cause cutaneous infarction and progressive necrotic ulceration. Mortality remains around 50–80% at one year. Clinically critical in skin oncology because the necrotic ulcers — particularly on the lower limbs, abdomen and breast — closely mimic cSCC, livedoid vasculopathy, vasculitis or necrotising soft-tissue infection. Treatment combines sodium thiosulphate, correction of calcium-phosphate metabolism, cessation of warfarin and meticulous wound care.

CurrentLast reviewed 15 May 2026
Clinical image of Calciphylaxis
Calciphylaxis. Image sourced from DermNet New Zealand. Used under CC BY-NC-ND 4.0. No endorsement implied.

Clinical features

  • Painful violaceous patches or plaques progressing rapidly to necrotic, eschar-covered ulcers.
  • Net-like, livedoid retiform purpura is characteristic at the periphery.
  • Pain is severe and out of proportion to lesion size.
  • Two distinct distributions:
    • Central (truncal — abdomen, breast, buttock, proximal limb) — worse prognosis.
    • Distal / acral (lower limbs, fingers / toes) — typically less severe.
  • Wounds expand rapidly; secondary infection common; sepsis is the leading cause of death.

Risk factors

  • End-stage renal disease on haemodialysis (commonest setting) or peritoneal dialysis.
  • Female sex.
  • Obesity.
  • Diabetes mellitus.
  • Hyperparathyroidism / secondary or tertiary; elevated calcium-phosphate product.
  • Warfarin use — inhibits vitamin-K-dependent matrix Gla protein, predisposing to vascular calcification.
  • Vitamin K deficiency.
  • Hypoalbuminaemia.
  • Recent rapid changes in calcium / phosphate / PTH balance.
  • Non-uraemic calciphylaxis — primary hyperparathyroidism, malignancy, autoimmune, alcoholic liver disease.

Diagnosis

  • Clinical pattern in an at-risk patient is highly suggestive.
  • Biopsy — deep punch or incisional from the edge of the lesion:
    • Calcium deposits within the walls of small-to-medium-calibre vessels (von Kossa / alizarin red staining).
    • Intimal hyperplasia, microthrombi, surrounding panniculitis and dermal necrosis.
    • Biopsy carries pathergy / wound-extension risk — discuss risk-benefit; small punch from edge is reasonable.
  • Bloods — U&E, calcium, phosphate, calcium-phosphate product, PTH, vitamin D, vitamin K status, INR if on warfarin.
  • Imaging — plain radiograph or bone scintigraphy showing soft-tissue and vascular calcification.
  • Multidisciplinary input — renal medicine, dermatology, plastic surgery / tissue viability, pain medicine.

Management

  • Sodium thiosulphate 25 g IV three times weekly post-dialysis — chelator and antioxidant; first-line UK pharmacological therapy.
  • Correct calcium-phosphate balance — low-calcium dialysate, non-calcium phosphate binders (sevelamer, lanthanum), cinacalcet for secondary hyperparathyroidism, parathyroidectomy in selected cases.
  • Cessation of warfarin — convert to apixaban or rivaroxaban where anticoagulation indicated.
  • Vitamin K supplementation — emerging evidence supports addition.
  • Wound care — non-adherent dressings, no aggressive debridement (pathergy risk); hyperbaric oxygen therapy in selected cases.
  • Pain control — opioids, ketamine, regional anaesthesia; pain is often debilitating.
  • Treatment of sepsis — broad-spectrum antibiotics, surgical drainage where infection requires.
  • Multidisciplinary palliative-care input — high mortality and treatment burden often warrant early symptom-management planning.

Prognosis

  • One-year mortality 50–80%; central / truncal distribution worse than distal.
  • Sepsis from wound infection is the leading cause of death.
  • Survivors often have prolonged hospitalisation, repeated debridement and chronic pain.
  • Despite low-quality evidence, early multidisciplinary intervention improves outcomes — high index of suspicion is essential.

References

  1. Nigwekar SU, Thadhani R, Brandenburg VM. Calciphylaxis. N Engl J Med; 2018.
  2. Hayashi M et al. Sodium thiosulfate in the treatment of calciphylaxis. Clin J Am Soc Nephrol; 2013.
  3. UK Kidney Association. Calciphylaxis rare renal disease information. UKKA Rare Renal patient and clinician information, accessed 18 May 2026.

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