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POEMS syndrome with opticneuritis as initial symptom: a case report
Yuanyuan Liu1, Weiping Lu1, Hong Zhang1
1Doctor, Department of Endocrinology, The Huai-an First Affiliated Hospital of Nanjing Medical University, Jiangsu, China.
A rare paraneoplastic syndrome, POEMS syndrome, was diagnosed in a 30-year-old female presenting with vision loss and neuropathy. The diagnosis was confirmed after extensive testing revealed organomegaly, endocrinopathy, M-protein, and skin changes.
Area of Science:
- Endocrinology
- Neurology
- Oncology
Background:
- Polyneuropathy, Organomegaly, Endocrinopathy, M-protein and Skin changes syndrome (POEMS) is a rare plasma cell dyscrasia.
- It commonly manifests as peripheral neuropathy but can present with diverse symptoms.
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