{
  "abstract": "Pyoderma gangrenosum (PG) is a rare neutrophilic dermatosis not only characterised by rapidly progressive skin ulceration, often triggered by trauma or surgery, but also associated with malignancy as a paraneoplastic condition. This case report describes a female patient in her early 70s who developed PG following a total abdominal hysterectomy, bilateral salpingo-oophorectomy and omentectomy for stage IVB high-grade serous carcinoma of the endometrium. This case highlights the diagnostic challenges, the role of early multidisciplinary involvement, investigation and appropriate therapeutic interventions.",
  "authors": [
    {
      "affiliations": [
        "Gynaecology Oncology, Swansea Bay University Health Board, Swansea, UK"
      ],
      "name": "Rafeef Abu Shamleh"
    },
    {
      "affiliations": [
        "Gynaecology Oncology, Swansea Bay University Health Board, Swansea, UK"
      ],
      "name": "Ahmad Souriti"
    },
    {
      "affiliations": [
        "Gynaecology Oncology, Swansea Bay University Health Board, Swansea, UK"
      ],
      "name": "Patrick Keating"
    },
    {
      "affiliations": [
        "Gynaecology Oncology, Swansea Bay University Health Board, Swansea, UK"
      ],
      "name": "Nagindra Das"
    }
  ],
  "title": "Pyoderma gangrenosum of the abdominal wall skin in a postoperative gynaecologic oncology patient",
  "uid": "e97d48cc-2f9c-5cd2-94de-c8e5ad269aa0"
}
