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Virtual case of the month
Perineal mass in a 50-year-old man
  1. Ameer Aldarragi1,
  2. Magnus Hallin2,
  3. Robin L Jones2,3,
  4. Omar L Qassid4,
  5. Cyril Fisher3,5,
  6. Iskander Chaudhry6,
  7. Khin Thway2,3
  1. 1 School of Medicine, University of Liverpool, Liverpool, England, UK
  2. 2 Sarcoma Unit, The Royal Marsden Hospital, London, South West England, UK
  3. 3 The Institute of Cancer Research, London, South West England, UK
  4. 4 University Hospitals of Leicester, Infirmary Square, Leicester, Leicestershire, UK
  5. 5 Department of Musculoskeletal Pathology, Royal Orthopaedic Hospital NHS Foundation Trust, Robert Aitken Institute for Clinical Research, University of Birmingham, Birmingham, England, UK
  6. 6 Department of Histopathology, Royal Liverpool and Broadgreen University Hospitals NHS Trust, L7 8XP, UK, Liverpool, England, United Kingdom
  1. Correspondence to Dr Khin Thway, Sarcoma Unit, The Royal Marsden Hospital, London, SW3 6JJ, UK; khin.thway{at}rmh.nhs.uk

http://dx.doi.org/10.1136/jclinpath-2019-206337

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    Clinical history

    A man in his fifties presented with a lump in his left anal/perineal region, which was clinically thought to be a lipoma and was excised. No preoperative imaging was available. Review the high-quality, interactive digital Aperio slide at http://virtualacp.com/JCPCases/jclinpath-2019-206337/ and consider your diagnosis.

    What is your diagnosis?

    1. Epithelioid angiosarcoma (EAS).

    2. Epithelioid malignant peripheral nerve sheath tumour (eMPNST).

    3. Malignant rhabdoid tumour (MRT).

    4. Melanoma.

    5. Proximal epithelioid sarcoma (ES).

    6. Pseudomyogenic haemangioendothelioma (PH).

    The correct answer is after the Discussion.

    Discussion

    The diagnosis in this case is proximal ES. This was based on the following morphological features and immunohistochemistry. The sections show a cellular tumour composed of large polygonal cells with vesicular nuclei with prominent nucleoli and abundant eosinophilic granular cytoplasm (figure 1A). There are 8 mitoses per 10 high-power fields and focal necrosis. The tumour grows in sheets to form large nodules with a mild intratumoural lymphoid population and infiltrates into the surrounding fibroadipose tissue. The morphology and the immunohistochemistry findings are in keeping with proximal-variant epithelioid sarcoma (PES). The tumour shows strong and diffuse expression of epithelial membrane antigen (EMA) and CD34, with patchy expression of AE1/AE3 (figure 1B,C). There is also loss of nuclear expression of INI1 (figure 1D). There is no expression of MNF116, CAM5.2, S100 protein, CD30, CD31, FLI1, ERG, SOX10, HMB45, MelanA, desmin, smooth muscle actin (SMA), myogenin, CD45, PLAP or prostate-specific antigen.

    Figure 1

    Scanned virtual slide (proximal-type ES). Proximal-type ES. (A) The tumour is composed of sheets and nests of relatively large and monomorphic epithelioid cells with vesicular nuclei and prominent nucleoli. (B,C) There is diffuse and strong expression of CD34 (B) and epithelial …

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    Footnotes

    • Handling editor Dhirendra Govender.

    • Twitter @QassidO

    • Contributors AA, MH, RLJ, OLQ, CF, IC and KT all cowrote the manuscript. MH and KT selected and photographed the images.

    • Funding The authors have not declared a specific grant for this research from any funding agency in the public, commercial or not-for-profit sectors.

    • Competing interests None declared.

    • Patient consent for publication Not required.

    • Provenance and peer review Not commissioned; internally peer reviewed.