{
  "abstract": "Adenopathy and an extensive skin patch overlying a plasmacytoma (AESOP) syndrome is a rare condition characterised by an erythemato-violaceous patch on the skin, accompanied by an underlying solitary plasmacytoma. It may give an early clue for the diagnosis of polyneuropathy, organomegaly, endocrinopathy, monoclonal protein, skin changes (POEMS) syndrome, an uncommon multisystem disorder driven by plasma cell dyscrasia. We describe a 62-year-old man with sensorimotor peripheral neuropathy, unintentional weight loss and a persistent skin rash. Diagnostic findings, including elevated vascular endothelial growth factor, an immunoglobulin A kappa paraprotein and a skin/sternal biopsy, led to the diagnosis of AESOP and POEMS syndrome. This case underscores the importance of early recognition of AESOP syndrome as a potential lifesaving clue for the early diagnosis of POEMS syndrome.",
  "authors": [
    {
      "affiliations": [
        "University Hospital Southampton NHS Foundation Trust Wessex Neurological Centre, Southampton, UK"
      ],
      "name": "Joumana Freiha"
    },
    {
      "affiliations": [
        "Department of Haematology, Southampton University Hospitals NHS Trust, Southampton, England, UK"
      ],
      "name": "Clare Lodwick"
    },
    {
      "affiliations": [
        "Department of Pathology, Southampton University Hospitals NHS Trust, Southampton, England, UK"
      ],
      "name": "Heather Roche"
    },
    {
      "affiliations": [
        "Neurosciences, Wessex Neurological Centre, Southampton, UK"
      ],
      "name": "Chinar Osman"
    }
  ],
  "title": "AESOP syndrome: a rare and early indicator of POEMS syndrome",
  "uid": "6b8a1bae-2ca8-5fda-ab20-87c8699d44a2"
}