Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2018 Sep 14:3:62.
doi: 10.21037/tgh.2018.09.02. eCollection 2018.

Vascular tumours of the liver: a particular story

Affiliations
Review

Vascular tumours of the liver: a particular story

Jan Lerut et al. Transl Gastroenterol Hepatol. .

Abstract

Vascular tumours of the liver represent an underrated chapter of medical and surgical hepatology. These tumours cover a wide spectrum ranging from the frequent and most benign hepatic haemangioma (HH), via the rare and intermediately aggressive hepatic epithelioid haemangioendothelioma (HEHE) to the rare and most malignant hepatic haemangiosarcoma (HHS). In contrast to the treatment algorithms for hepatocellular and cholangiocellular cancer, the diagnostic and therapeutic approaches to HEHE and HHS are not well developed. The related uncertainty is explained by their rare occurrence and their protean clinical, morphological (imaging) and histopathological presentation and behaviour. This article gives an update about these particular tumours based on the analysis of the recent literature and of the studies on vascular tumours published by the European Liver Intestine Transplantation Association (ELITA)-European Liver Transplant Registry (ELTR). It focuses also on the place of liver transplantation (LT) in the respective therapeutic algorithms. The differential diagnosis between these vascular and other tumour types may be very difficult. Correct diagnosis is of utmost importance and is based on a high index of clinical suspicion and on the integration of clinical, radiological, histological [including immunohistochemistry (IHC) and molecular biology findings]. Surgery, be it partial or total hepatectomy (LT), should be proposed whenever possible, because it is the therapeutic mainstay. In HEHE, LT provides excellent results, with long-term disease-free survivals (DFS) reaching 75%. Good results can be obtained even in case of (frequent) extrahepatic spread. Based on the extensive ELITA-ELTR study a HEHE-LT prognostic score has been proposed in order to estimate the risk of recurrence after LT. In contrast, results of surgery and LT are extremely poor for HHS, for the almost invariably rapid recurrence (within 6 months) and related death within 2 years. LT remains a contraindication for HHS. Due to the still important recurrence rate after surgical resection (25% in HEHE and almost 100% in HHS), there is an urgent need to develop pharmacological treatments targeting angiogenic and non-VEGF angiogenic pathways. To date, some prospective pilot studies and case reports have shown some short-term stabilisation of the disease in small groups of patients. In order to make progress, combination of surgery, anti-angiogenic and immunotherapy seems worthwhile. To complete the panel of vascular liver tumours, infantile haemangioendothelioma, haemangiopericytoma, nodular regenerative hyperplasia (NRH) and hepatic small vessel neoplasms (HSVN) are also discussed.

Keywords: Liver neoplasms; haemangiopericytoma; hepatectomy; hepatic epithelioid haemangioendothelioma; hepatic haemangioma; hepatic haemangiomatosis; hepatic haemangiosarcoma; hepatic infantile haemangioendothelioma; hepatic small vessel neoplasms; liver transplantation; nodular regenerative hyperplasia; vascular tissue.

PubMed Disclaimer

Conflict of interest statement

Conflicts of Interest: The authors have no conflicts of interest to declare.

Figures

Figure 1
Figure 1
Therapeutic algorithm for hepatic epithelioid haemangioendothelioma. *, non-standardized neo-adjuvant approach; **, histological examination combining immunohistochemistry and H&E staining. HEHE, hepatic epithelioid haemangioendothelioma; CHTH, chemotherapy; EHD, extrahepatic disease; FU, follow-up; IS, immunosuppression; HHS, hepatic haemangiosarcoma; LT, liver transplantation.

References

    1. Bridgewater J, Galle PR, Khan SA, et al. Guidelines for the diagnosis and management of intrahepatic cholangiocarcinoma. J Hepatol 2014;60:1268-89. 10.1016/j.jhep.2014.01.021 - DOI - PubMed
    1. European Association for the Study of the Liver. European Association for the Study of the Liver EASL Clinical Practice Guidelines: Management of hepatocellular carcinoma. J Hepatol 2018;69:182-236. 10.1016/j.jhep.2018.03.019 - DOI - PubMed
    1. Ishak K, Goodman Z, Stocker J. Tumors of the liver and intrahepatic bile ducts. Atlas of tumour pathology. Third series, fascicle 31. Armed Forces Institute of Pathology, Washington, 1999.
    1. Sempoux C, Balabaud C, Paradis V, et al. Hepatocellular nodules in vascular liver diseases. Virchows Arch 2018;473:33-44. 10.1007/s00428-018-2373-6 - DOI - PubMed
    1. Valla DC, Cazals-Hatem D. Vascular liver diseases on the clinical side: definitions and diagnosis, new concepts. Virchows Arch 2018;473:3-13. 10.1007/s00428-018-2331-3 - DOI - PubMed