Sensory-Motor Polyneuropathy and Digital Ischemia: A Rare Presentation of Granulomatosis with Polyangiitis

Wasundara Wathurapatha1, B G A Rathnamali1, Upul Dissanayake1

  • 1National Hospital of Sri Lanka, Colombo, Sri Lanka.

Insights

Granulomatosis with polyangiitis (GPA) can rarely present with peripheral sensory-motor polyneuropathy and digital gangrene. Early diagnosis and aggressive immunosuppression are crucial for recovery in these rare GPA cases.

Area of Science:

  • Vascular Medicine
  • Neurology
  • Rheumatology

Background:

  • Granulomatosis with polyangiitis (GPA) commonly affects the respiratory tract and kidneys.
  • Peripheral nervous system involvement in GPA typically manifests as mononeuritis multiplex.
  • Peripheral sensory-motor polyneuropathy and digital gangrene are exceptionally rare presenting features of GPA.

Observation:

  • A 46-year-old woman presented with severe peripheral sensorimotor polyneuropathy in her lower limbs.
  • Her symptoms were preceded by a purpuric rash and painful ulcers on the lower limbs.
  • She also exhibited digital ischemia and dry gangrene of the left 4th toe.

Findings:

  • Diagnosis of GPA was confirmed via skin biopsy, positive ANCA serology, and clinical evaluation.
  • The patient received aggressive immunosuppressive therapy with methylprednisolone and cyclophosphamide.
  • She was maintained on prednisolone and azathioprine for long-term management.

Implications:

  • This case underscores the importance of considering GPA in patients with unexplained peripheral neuropathy and digital ischemia.
  • It highlights the need for a broad differential diagnosis in neurological presentations.
  • Prompt recognition and treatment of rare GPA manifestations can lead to favorable patient outcomes.

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