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POEMS syndrome: a unique presentation and a diagnostic challenge
Daniel Farrugia1, David James Camilleri2, Janice Azzopardi2
1Haematology, Mater Dei Hospital, Msida, Malta daniel.f.farrugia@gov.mt.
A rare case of POEMS syndrome presented as myositis and polyneuropathy. Early diagnosis is crucial as this condition, characterized by plasmacytoma, can lead to severe disability if treatment is delayed.
Area of Science:
- Neurology
- Oncology
Background:
- POEMS syndrome is a rare multisystem disorder.
- It can present with diverse neurological symptoms, including myositis and polyneuropathy.
Observation:
- A 70-year-old female presented with gait deterioration and MRI findings suggestive of myositis.
- Muscle biopsy and nerve conduction studies revealed neurogenic amyotrophy and mixed sensorimotor polyneuropathy.
Findings:
- Positron emission tomography scan identified a hip lesion, biopsied as a plasmacytoma.
- Despite normal serum protein electrophoresis, the findings confirmed POEMS syndrome.
Implications:
- Delayed diagnosis of POEMS syndrome can lead to irreversible neurological damage and dependence.
- This case highlights the importance of considering POEMS syndrome in patients with unexplained myositis and polyneuropathy, even with atypical initial findings.
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