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Subkutant myksopapillært ependymom

Forfatter(e)
Niels Bjørn1, Morten Søe2 & Sönke Detlefsen3 1) Organkirurgisk Afdeling D, Sygehus Lillebælt, Kolding 2) Neurokirurgisk Afdeling, Odense Universitetshospital 3) Afdeling for Klinisk Patologi, Odense Universitetshospital Ugeskr Læger 2015;177:V03150235
Reference: 
Ugeskr Læger 2015;177:V03150235
Blad nummer: 
Sidetal: 
2-3
Subcutaneous myxopapillary ependymoma
Subcutaneous myxopapillary ependymoma is a very rare entity, and to our knowledge this is the first published case from Denmark. A previously healthy 32-year-old male pre­sented with subcutaneous swelling and tenderness located at the top of the intergluteal cleft. The circular soft tumour, measuring 1.7 × 1.7 × 1.2 cm, was removed surgically. After histopathological examination with several immuno­histo­chemical and special stainings, the diagnosis surprisingly was subcutaneous myxopapillary ependymoma. The tumour was removed with free margins and no metastases were found on follow-up CT- and MRI scans.
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