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Rar liver tumour — epithelioid haemangioendothelioma: a case report

  • Sniedze Laivacuma*
  • , Indra Zeltiņa
  • , Aleksejs Derovs
  • , Andris Norko
  • , Sergejs Isajevs
  • , Karīna Makejeva
  • , Joost P.H. Drenth
  • *Šī darba korespondējošais autors
    • Riga Stradins University
    • University of Latvia
    • Riga East University Hospital
    • Radboud University Nijmegen

    Zinātniskās darbības rezultāts: Devums žurnālamZinātniskais raksts (žurnālā)koleģiāli recenzēts

    Kopsavilkums

    Epithelioid haemangioendothelioma (EHE) is a rare vascular soft tissue malignant tumour with unknown etiology; the estimated prevalence of EHE is less than one in 1 million. A 56-year-old man was admitted in our department due to pain in the right side of the abdomen lasting for two years and weight loss up to 10 kg. Since 2012, the patient underwent lung and abdominal CT scanning as well as biopsy, however the diagnosis was challenging. In 2015, repeated abdominal CT scanning and a liver core biopsy was performed. The epithelioid haemangioendothelioma was diagnosed based by histopathological examination with subsequent radiological and clinical correlation. Therefore, accurate histopathological examination with radiological and clinical correlation is essential in the diagnosis of epithelioid haemangioendothelioma.

    OriģinālvalodaAngļu
    Lapas (no-līdz)674-678
    ŽurnālsProceedings of the Latvian Academy of Sciences, Section B: Natural, Exact, and Applied Sciences
    Sējums76
    Izdevuma numurs5-6
    DOIs
    Publikācijas statussPublicēts - 1 dec. 2022

    OECD Zinātnes nozare

    • 3. Medicīnas un veselības zinātnes

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