Please use this identifier to cite or link to this item: 10.2478/prolas-2022-0103
Title: Rare liver tumour - epithelioid haemangioendothelioma: a case report
Authors: Laivacuma, Sniedze
Zeltiņa, Indra
Derovs, Aleksejs
Norko, Andris
Isajevs, Sergejs
Makejeva, Karīna
PH Drenth, Joost
Department of Infectology
Department of Internal Diseases
Keywords: Rar liver tumour;epithelioid haemangioendothelioma;3.2 Clinical medicine;1.1. Scientific article indexed in Web of Science and/or Scopus database
Issue Date: 1-Dec-2022
Citation: Laivacuma , S , Zeltiņa , I , Derovs , A , Norko , A , Isajevs , S , Makejeva , K & PH Drenth , J 2022 , ' Rare liver tumour - epithelioid haemangioendothelioma: a case report ' , Proceedings of the Latvian Academy of Sciences. Section B. Natural, Exact, and Applied Sciences. , vol. 76 , no. 5/6 , pp. 674-678 . https://doi.org/10.2478/prolas-2022-0103
Abstract: 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.
Description: Publisher Copyright: © 2022 Sniedze Laivacuma et al., published by Sciendo.
DOI: 10.2478/prolas-2022-0103
ISSN: 2255-890X
Appears in Collections:Research outputs from Pure / Zinātniskās darbības rezultāti no ZDIS Pure

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