Authors:
Gabor Mohos Department of Radiology, Medical Imaging Centre, Semmelweis University 1082 Budapest, Korányi Sándor street 2., Hungary
Department of Interventional Radiology, Heart and Vascular Centre, Semmelweis University 1122 Budapest, Határőr street 18., Hungary

Search for other papers by Gabor Mohos in
Current site
Google Scholar
PubMed
Close
https://orcid.org/0000-0002-9626-2325
,
Adam Zoltan Farkas Department of Interventional Radiology, Heart and Vascular Centre, Semmelweis University 1122 Budapest, Határőr street 18., Hungary

Search for other papers by Adam Zoltan Farkas in
Current site
Google Scholar
PubMed
Close
https://orcid.org/0000-0003-4612-380X
,
Andras Bibok Department of Interventional Radiology, Heart and Vascular Centre, Semmelweis University 1122 Budapest, Határőr street 18., Hungary

Search for other papers by Andras Bibok in
Current site
Google Scholar
PubMed
Close
https://orcid.org/0000-0003-0816-6083
,
David Adam Korda Department of Interventional Radiology, Heart and Vascular Centre, Semmelweis University 1122 Budapest, Határőr street 18., Hungary

Search for other papers by David Adam Korda in
Current site
Google Scholar
PubMed
Close
https://orcid.org/0000-0002-6448-0053
,
Oszkar Hahn Department of Surgery, Transplantation and Gastroenterology, Semmelweis University, 1082 Budapest, Üllői út 78., Hungary

Search for other papers by Oszkar Hahn in
Current site
Google Scholar
PubMed
Close
https://orcid.org/0000-0002-2127-9181
,
Attila Doros Department of Interventional Radiology, Heart and Vascular Centre, Semmelweis University 1122 Budapest, Határőr street 18., Hungary

Search for other papers by Attila Doros in
Current site
Google Scholar
PubMed
Close
https://orcid.org/0000-0002-6496-9895
,
Pal Akos Deak Department of Interventional Radiology, Heart and Vascular Centre, Semmelweis University 1122 Budapest, Határőr street 18., Hungary

Search for other papers by Pal Akos Deak in
Current site
Google Scholar
PubMed
Close
https://orcid.org/0000-0003-3881-837X
, and
Denes Balazs Horvathy Department of Interventional Radiology, Heart and Vascular Centre, Semmelweis University 1122 Budapest, Határőr street 18., Hungary

Search for other papers by Denes Balazs Horvathy in
Current site
Google Scholar
PubMed
Close
https://orcid.org/0000-0001-8136-7100
Open access

Abstract

We report a case of a female patient in her 40s who presented with right upper quadrant pain and abdominal discomfort. Surgical removal was not possible due to the location of the lesion. Between 2021 and 2022, the patient had four additional sessions of conventional transarterial embolization (TAE) with Lipiodol, but none succeeded in sufficiently reducing the hemangioma's size or permanently improving the symptoms. In November 2022, we used transarterial chemoembolization (TACE) with a Bleomycin-Lipiodol emulsion. Follow-up MRI scans showed a gradual reduction in the hemangioma volume, but the symptoms only improved partially. Hence, the patient underwent a second bleomycin TACE embolization in November 2023. By August 2024, control showed a total volume reduction of 409 cm³ (56%) and significant symptom improvement. This case demonstrates that Bleomycin-Lipiodol TACE can effectively reduce the size of giant liver hemangiomas, even after the failure of other interventional therapies.

Abstract

We report a case of a female patient in her 40s who presented with right upper quadrant pain and abdominal discomfort. Surgical removal was not possible due to the location of the lesion. Between 2021 and 2022, the patient had four additional sessions of conventional transarterial embolization (TAE) with Lipiodol, but none succeeded in sufficiently reducing the hemangioma's size or permanently improving the symptoms. In November 2022, we used transarterial chemoembolization (TACE) with a Bleomycin-Lipiodol emulsion. Follow-up MRI scans showed a gradual reduction in the hemangioma volume, but the symptoms only improved partially. Hence, the patient underwent a second bleomycin TACE embolization in November 2023. By August 2024, control showed a total volume reduction of 409 cm³ (56%) and significant symptom improvement. This case demonstrates that Bleomycin-Lipiodol TACE can effectively reduce the size of giant liver hemangiomas, even after the failure of other interventional therapies.

Introduction

Giant liver hemangiomas are venous vascular malformations, variably defined as lesions larger than 4–6 cm [1]. While often asymptomatic, they can cause abdominal pain in symptomatic cases. Management of symptomatic hemangiomas is controversial, with no established consensus [2–4]. In addition to surgical treatment, interventional options such as embolization and percutaneous sclerotization with a bleomycin-lipiodol emulsion are widely recognized for their efficacy [2, 5]. We report a case where a symptomatic giant liver hemangioma refractory to conventional TAE was successfully treated with transarterial bleomycin TACE.

Case presentation

Initially, In 2011, a 30-year-old female patient presented with right lower quadrant pain. Sonography incidentally revealed three small hemangiomas in her liver in segments five and six. The patient was advised to follow up, but she did not return until 2015 when she experienced abdominal discomfort. Imaging revealed significant growth of the hemangiomas, with the largest in the right lobe measuring 79 × 64 × 61 mm (251 cm3). Based on the symptoms, we assessed treatment options for the lesion adjacent to the right portal vein. The surgical opinion indicated that the only way to remove the giant hemangioma was through right hemihepatectomy, which was deemed too invasive for a benign lesion. For this reason, we decided to pursue interventional treatment for the giant hemangioma.

In June 2015, the patient underwent a superselective Transarterial Embolization (TAE) with 8 mL of Lipiodol, followed by a microwave ablation in December 2015 (multiple positions on 60 W, during 5–5 min). Initial size reduction was observed, but despite these interventions, follow-up imaging in 2016 showed growth of the lesion to 89 mm (188 cm3). The patient dropped out of follow-up, probably due to the lack of considerable sympthoms. She presented again after a five-years, with recurring, sometimes sever abdominal pain in the right upper quadrant of the abdomen. By this time the lesion has grown to 673 cm3. At the beginning we believed that controlling the size (preventing further growth) could be a satisfactory outcome. For this reason, four TAE sessions have been performed between 2021 and 2022 using 10 mL of Lipiodol in each session. We observed a transient reduction in complaints following the treatments, which we considered a partial clinical success. However, no size reduction was achieved; on contrary the lesion showed further growth.

Due to persistent symptoms, in November 2022, we performed TACE with bleomycin-lipiodol emulsion (right brachial approach, 4F introducer, 4F H1 catheter and 2.7 F microcatheter). The preparation involved 15,000 unit of bleomycin in 5 cm3 of saline mixed with 10 mL lipiodol. The procedure was performed via right brachial access and involved embolizing three feeding branches with a total of 12 mL of the emulsion. Subsequent MRIs in 2023 demonstrated a gradual volume reduction of 221 cm3 (28%), but the desired outcome was not fully achieved. In November 2023, we repeated the TACE using the same method, resulting in a total volume reduction of 409 cm³ (56%) by August 2024, over a 21-month follow-up period (Figs 1 and 2).

Fig. 1.
Fig. 1.

Timeline of the giant heamangioma volume measurments. MWT indicates the time of the microwave thermoablation, dashed line indicates the TAE treatments, dash-dotted line indicates TACE treatments with belomycin

Citation: Imaging 2025; 10.1556/1647.2024.00286

Fig. 2.
Fig. 2.

Panel A shows coronal T2 MRI image of the giant heamangioma prior to the TACE treatments. Panel B shows coronal T2 MRI image 6 months after the second TACE. Panel C shows bulging of the haemangioma in supine position, while panel D demonstrates the cosmetic results six months after the last treatment

Citation: Imaging 2025; 10.1556/1647.2024.00286

Discussion

Liver hemangiomas are often asymptomatic but can cause significant discomfort due to mass effect. Complications, such as rupture, are rare; therefore, without symptoms, observation is a safe choice to monitor if they grow. In symptomatic cases, on the other hand, there is currently no consensus on the optimal management. Surgery might seem too invasive, while conventional TAE might not decrease the size and symptoms sufficiently. Several studies have shown that Bleomycin-lipiodol emulsion, including hundreds of patients, is a safe and sufficient option for treating giant symptomatic cases [2, 6, 7].

In our present case, another interventional option, namely microwave thermoablation combined with conventional TAE, was used as the first treatment in 2015. This resulted in a significant size reduction (before treatment: 251 cm^3, after treatment: 188 cm^3), while the patient's original uncertain complaints also improved. Probably, this is the reason why she did not show up for follow-up until her complaints became unbearable in 2021 with a visible bulging of the tumor. By that time, the hemangioma was 673 cm^3. The patient reported that her symptoms are mild in the morning and worsen throughout the day.

The patient had been taking contraceptives prior to her illness; however, she discontinued them as soon as the growth of the hemangioma was confirmed in 2015. Based on this, we assume that contraceptive use played a minimal or negligible role in the growth of the hemangioma. It is more important to note that the hemangioma was located in segment 5 and it was exophytic, so there was no liver parenchyma caudal to the lesion. Additionally, the patient had a standing job, which could explain the enormous growth of the lesion and the complaints getting worse throughout the day. At this point, we have applied four sessions of conventional TAE [8], but the hemangioma kept growing, along with the symptoms. We chose conventional TAE because bleomycin TACE was less widespread back then, and we tried to avoid using a cytotoxic agent in a young patient with a benign lesion. While NBCA or particles could also have been considered viable options, we determined that these materials would likely have remained permanently within the haemangioma, potentially stabilizing its size without achieving significant reduction. Given the lesion's pronounced bulging into the abdomen and the exophytic nature causing severe symptoms, achieving size reduction was considered essential.

Following bleomycin TACE, significant volume reduction was achieved, along with improved symptoms and cosmetic outcomes (Figs 1 and 2). After 2 sessions of bleomycin TACE, 56% of size reduction was achieved, comparable to literature data [2, 6, 7].

Since one bleomycin TACE resulted only in a 28% volume reduction, significantly less than literature data [2, 6, 7], we hypothesize that previous TAE sessions decreased the treatment's potential by blocking the vessels. Further studies are needed to investigate this hypothesis, but bleomycin TACE should be considered if a giant liver hemangioma seems to be resistant to conventional TAE treatment.

Conclusion

Our present case shows that bleomycin TACE can successfully decrease the size of giant liver hemangiomas even after several unsuccessful TAE sessions.

Conflict of interests

None to declare.

Authors' contribution

Conceptualization DBH and AD; GM and DBH compiled all relevant information concerning the presented case and did the literature review. AD, PAD, OH, AZF, AB, DAK, GM and DBH evaluated the whole treatment of the patients. GM and DBH wrote and prepared the original draft; GM and DBH made the visualisation. AZF, AB, DAK, OH reviewed and edited the manuscript. All authors have read and agreed to the published version of the manuscript.

Ethical statement

All procedures performed in this study involving human participants were in accordance with the ethical standards of the institutional research committee and with the 1964 Helsinki Declaration and its later amendments or comparable ethical standards.

Informed consent

Informed consent was obtained from the participant included in this report.

Funding sources

This study was not supported by any funding.

Acknowledgements

We are grateful to Peter Molnar (Semmelweis University, Medical Imaging Centre) for performing the MRI scans of this present case.

References

  • [1]

    Coumbaras M, Wendum D, Monnier-Cholley L, Dahan H, Tubiana JM, Arrivé L: CT and MR imaging features of pathologically proven atypical giant hemangiomas of the liver .AJR Am J Roentgenol 2002; 179(6): 14571463.

    • Search Google Scholar
    • Export Citation
  • [2]

    Torkian P, Li J, Kaufman JA, Jahangiri Y: Effectiveness of transarterial embolization in treatment of symptomatic hepatic hemangiomas: systematic review and meta-analysis .Cardiovasc Intervent Radiol 2021; 44(1): 8091.

    • Search Google Scholar
    • Export Citation
  • [3]

    Hoekstra LT, Bieze M, Erdogan D, Roelofs JJ, Beuers UH, van Gulik TM: Management of giant liver hemangiomas: An update .Expert Rev Gastroenterol Hepatol 2013; 7(3): 263268.

    • Search Google Scholar
    • Export Citation
  • [4]

    Ketchum WA, Lin-Hurtubise KM, Ochmanek E, Ishihara K, Rice RD: Management of symptomatic hepatic “mega” hemangioma .Hawaii J Med Public Health 2019; 78(4): 128131.

    • Search Google Scholar
    • Export Citation
  • [5]

    Ayoobi Yazdi N, Mehrabinejad MM, Dashti H, Pourghorban R, Nassiri Toosi M, Rokni Yazdi H: Percutaneous sclerotherapy with bleomycin and ethiodized oil: a promising treatment in symptomatic giant liver hemangioma .Radiology 2021; 301(2): 464471.

    • Search Google Scholar
    • Export Citation
  • [6]

    Yuan B, Zhang J-L, Duan F, Wang M-Q: Medium and long-term outcome of superselective transcatheter arterial embolization with lipiodol-bleomycin emulsion for giant hepatic hemangiomas: results in 241 patients .J Clin Med 2022; 11(16).

    • Search Google Scholar
    • Export Citation
  • [7]

    Kacała A, Dorochowicz M, Patrzałek D, Janczak D, Guziński M: Safety and feasibility of transarterial bleomycin-lipiodol embolization in patients with giant hepatic hemangiomas .Medicina (Kaunas) 2023; 59(8).

    • Search Google Scholar
    • Export Citation
  • [8]

    Srivastava DN, Gandhi D, Seith A, Pande GK, Sahni P: Transcatheter arterial embolization in the treatment of symptomatic cavernous hemangiomas of the liver: A prospective study .Abdom Imaging 2001; 26(5): 510514.

    • Search Google Scholar
    • Export Citation
  • [1]

    Coumbaras M, Wendum D, Monnier-Cholley L, Dahan H, Tubiana JM, Arrivé L: CT and MR imaging features of pathologically proven atypical giant hemangiomas of the liver .AJR Am J Roentgenol 2002; 179(6): 14571463.

    • Search Google Scholar
    • Export Citation
  • [2]

    Torkian P, Li J, Kaufman JA, Jahangiri Y: Effectiveness of transarterial embolization in treatment of symptomatic hepatic hemangiomas: systematic review and meta-analysis .Cardiovasc Intervent Radiol 2021; 44(1): 8091.

    • Search Google Scholar
    • Export Citation
  • [3]

    Hoekstra LT, Bieze M, Erdogan D, Roelofs JJ, Beuers UH, van Gulik TM: Management of giant liver hemangiomas: An update .Expert Rev Gastroenterol Hepatol 2013; 7(3): 263268.

    • Search Google Scholar
    • Export Citation
  • [4]

    Ketchum WA, Lin-Hurtubise KM, Ochmanek E, Ishihara K, Rice RD: Management of symptomatic hepatic “mega” hemangioma .Hawaii J Med Public Health 2019; 78(4): 128131.

    • Search Google Scholar
    • Export Citation
  • [5]

    Ayoobi Yazdi N, Mehrabinejad MM, Dashti H, Pourghorban R, Nassiri Toosi M, Rokni Yazdi H: Percutaneous sclerotherapy with bleomycin and ethiodized oil: a promising treatment in symptomatic giant liver hemangioma .Radiology 2021; 301(2): 464471.

    • Search Google Scholar
    • Export Citation
  • [6]

    Yuan B, Zhang J-L, Duan F, Wang M-Q: Medium and long-term outcome of superselective transcatheter arterial embolization with lipiodol-bleomycin emulsion for giant hepatic hemangiomas: results in 241 patients .J Clin Med 2022; 11(16).

    • Search Google Scholar
    • Export Citation
  • [7]

    Kacała A, Dorochowicz M, Patrzałek D, Janczak D, Guziński M: Safety and feasibility of transarterial bleomycin-lipiodol embolization in patients with giant hepatic hemangiomas .Medicina (Kaunas) 2023; 59(8).

    • Search Google Scholar
    • Export Citation
  • [8]

    Srivastava DN, Gandhi D, Seith A, Pande GK, Sahni P: Transcatheter arterial embolization in the treatment of symptomatic cavernous hemangiomas of the liver: A prospective study .Abdom Imaging 2001; 26(5): 510514.

    • Search Google Scholar
    • Export Citation
  • Collapse
  • Expand

Chair of the Editorial Board:
Béla MERKELY (Semmelweis University, Budapest, Hungary)

Editor-in-Chief:
Pál MAUROVICH-HORVAT (Semmelweis University, Budapest, Hungary)

Deputy Editor-in-Chief:
Viktor BÉRCZI (Semmelweis University, Budapest, Hungary)

Executive Editor:
Charles S. WHITE (University of Maryland, USA)

Deputy Editors:
Gianluca PONTONE (Department of Cardiovascular Imaging, Centro Cardiologico Monzino IRCCS, Milan, Italy)
Michelle WILLIAMS (University of Edinburgh, UK)

Senior Associate Editors:
Tamás Zsigmond KINCSES (University of Szeged, Hungary)
Hildo LAMB (Leiden University, The Netherlands)
Denisa MURARU (Istituto Auxologico Italiano, IRCCS, Milan, Italy)
Ronak RAJANI (Guy’s and St Thomas’ NHS Foundation Trust, London, UK)

Associate Editors:
Andrea BAGGIANO (Department of Cardiovascular Imaging, Centro Cardiologico Monzino IRCCS, Milan, Italy)
Fabian BAMBERG (Department of Radiology, University Hospital Freiburg, Germany)
Péter BARSI (Semmelweis University, Budapest, Hungary)
Theodora BENEDEK (University of Medicine, Pharmacy, Sciences and Technology, Targu Mures, Romania)
Ronny BÜCHEL (University Hospital Zürich, Switzerland)
Filippo CADEMARTIRI (SDN IRCCS, Naples, Italy) Matteo CAMELI (University of Siena, Italy)
Csilla CELENG (University of Utrecht, The Netherlands)
Edit DÓSA (Semmelweis University, Budapest, Hungary)
Tilman EMRICH (University Hospital Mainz, Germany)

Marco FRANCONE (La Sapienza University of Rome, Italy)
Viktor GÁL (OrthoPred Ltd., Győr, Hungary)
Alessia GIMELLI (Fondazione Toscana Gabriele Monasterio, Pisa, Italy)
Tamás GYÖRKE (Semmelweis Unversity, Budapest)
Fabian HYAFIL (European Hospital Georges Pompidou, Paris, France)
György JERMENDY (Bajcsy-Zsilinszky Hospital, Budapest, Hungary)
Pál KAPOSI (Semmelweis University, Budapest, Hungary)
Mihaly KÁROLYI (University of Zürich, Switzerland)
Lajos KOZÁK (Semmelweis University, Budapest, Hungary)
Mariusz KRUK (Institute of Cardiology, Warsaw, Poland)
Zsuzsa LÉNARD (Semmelweis University, Budapest, Hungary)
Erica MAFFEI (ASUR Marche, Urbino, Marche, Italy)
Robert MANKA (University Hospital, Zürich, Switzerland)
Saima MUSHTAQ (Cardiology Center Monzino (IRCCS), Milan, Italy)
Gábor RUDAS (Semmelweis University, Budapest, Hungary)
Balázs RUZSICS (Royal Liverpool and Broadgreen University Hospital, UK)
Christopher L SCHLETT (Unievrsity Hospital Freiburg, Germany)
Bálint SZILVESZTER (Semmelweis University, Budapest, Hungary)
Richard TAKX (University Medical Centre, Utrecht, The Netherlands)
Ádám TÁRNOKI (National Institute of Oncology, Budapest, Hungary)
Dávid TÁRNOKI (National Institute of Oncology, Budapest, Hungary)
Ákos VARGA-SZEMES (Medical University of South Carolina, USA)
Hajnalka VÁGÓ (Semmelweis University, Budapest, Hungary)
Jiayin ZHANG (Department of Radiology, Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China)

International Editorial Board:

Gergely ÁGOSTON (University of Szeged, Hungary)
Anna BARITUSSIO (University of Padova, Italy)
Bostjan BERLOT (University Medical Centre, Ljubljana, Slovenia)
Edoardo CONTE (Centro Cardiologico Monzino IRCCS, Milan)
Réka FALUDI (University of Szeged, Hungary)
Andrea Igoren GUARICCI (University of Bari, Italy)
Marco GUGLIELMO (Department of Cardiovascular Imaging, Centro Cardiologico Monzino IRCCS, Milan, Italy)
Kristóf HISRCHBERG (University of Heidelberg, Germany)
Dénes HORVÁTHY (Semmelweis University, Budapest, Hungary)
Julia KARADY (Harvard Unversity, MA, USA)
Attila KOVÁCS (Semmelweis University, Budapest, Hungary)
Riccardo LIGA (Cardiothoracic and Vascular Department, Università di Pisa, Pisa, Italy)
Máté MAGYAR (Semmelweis University, Budapest, Hungary)
Giuseppe MUSCOGIURI (Centro Cardiologico Monzino IRCCS, Milan, Italy)
Anikó I NAGY (Semmelweis University, Budapest, Hungary)
Liliána SZABÓ (Semmelweis University, Budapest, Hungary)
Özge TOK (Memorial Bahcelievler Hospital, Istanbul, Turkey)
Márton TOKODI (Semmelweis University, Budapest, Hungary)

Managing Editor:
Anikó HEGEDÜS (Semmelweis University, Budapest, Hungary)

Pál Maurovich-Horvat, MD, PhD, MPH, Editor-in-Chief

Semmelweis University, Medical Imaging Centre
2 Korányi Sándor utca, Budapest, H-1083, Hungary
Tel: +36-20-663-2485
E-mail: maurovich-horvat.pal@med.semmelweis-univ.hu

Indexing and Abstracting Services:

  • WoS Emerging Science Citation Index
  • Scopus
  • DOAJ

2024  
Scopus  
CiteScore  
CiteScore rank  
SNIP  
Scimago  
SJR index 0.178
SJR Q rank Q4

2023  
Web of Science  
Journal Impact Factor 0.7
Rank by Impact Factor Q3 (Medicine, General & Internal)
Journal Citation Indicator 0.09
Scopus  
CiteScore 0.7
CiteScore rank Q4 (Medicine miscellaneous)
SNIP 0.151
Scimago  
SJR index 0.181
SJR Q rank Q4

Imaging
Publication Model Gold Open Access
Submission Fee none
Article Processing Charge none
Subscription Information Gold Open Access

Imaging
Language English
Size A4
Year of
Foundation
2020 (2009)
Volumes
per Year
1
Issues
per Year
2
Founder Akadémiai Kiadó
Founder's
Address
H-1117 Budapest, Hungary 1516 Budapest, PO Box 245.
Publisher Akadémiai Kiadó
Publisher's
Address
H-1117 Budapest, Hungary 1516 Budapest, PO Box 245.
Responsible
Publisher
Chief Executive Officer, Akadémiai Kiadó
ISSN 2732-0960 (Online)

Monthly Content Usage

Abstract Views Full Text Views PDF Downloads
Nov 2024 0 0 0
Dec 2024 0 0 0
Jan 2025 0 27 24
Feb 2025 0 1244 109
Mar 2025 0 875 43
Apr 2025 0 118 21
May 2025 0 0 0