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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.
Abstract:
Granulomatosis with polyangiitis (GPA) typically presents with upper or lower respiratory tract symptoms and/or with renal involvement. Although it can affect the peripheral nervous system frequently, with mononeuritis multiplex being the most common pattern, the occurrence of peripheral sensory-motor polyneuropathy as a presenting manifestation is distinctly rare. Prevalence of digital gangrene is also extremely rare in GPA. We describe a 46-year-old woman presenting with severe peripheral sensorimotor polyneuropathy affecting bilateral lower limbs preceded by a purpuric skin rash and multiple painful ulcers confined to the lower limbs. She had evidence of digital ischemia affecting multiple toes and dry gangrene of the left 4th toe. Diagnosis of GPA was made based on skin biopsy, positive ANCA serology, and clinical criteria. She made a good recovery following aggressive immunosuppressive treatment with methylprednisolone and cyclophosphamide and was maintained on prednisolone and azathioprine. This case highlights the importance of suspecting GPA in a patient presenting with sensorimotor polyneuropathy and/or digital ischemia even in the absence of more classic presenting features and underlies the necessity of accurate differential diagnosis in evaluating a case of peripheral neuropathy.
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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