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"Won Chang"

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"Won Chang"

Original Article

Non-contrast magnetic resonance imaging for detection of late recurrent hepatocellular carcinoma after curative treatment: a prospective multicenter comparison to contrast-enhanced computed tomography
Dong Wook Kim, Won Chang, So Yeon Kim, Young-Suk Lim, Jonggi Choi, Jungheum Cho, Jin-Wook Kim, Jai Young Cho, Sun Kyung Jeon, Yun Bin Lee, Eun Ju Cho, Su Jong Yu, Kyung-Suk Suh, Kwang-Woong Lee, Dong Ho Lee
Clin Mol Hepatol 2025;31(4):1285-1297.
Published online June 13, 2025
DOI: https://doi.org/10.3350/cmh.2025.0258
Background/Aims
Hepatocellular carcinoma (HCC) frequently recurs after curative treatment, posing challenges to long-term survival. Although contrast-enhanced multiphasic computed tomography (CECT) is commonly used for detecting recurrence, it is associated with risks such as radiation exposure and contrast agent reactions. This study aimed to compare the diagnostic performance of non-contrast magnetic resonance imaging (NC-MRI) with CECT for detecting recurrent HCC.
Methods
In this prospective multicenter intra-individual head-to-head comparison trial (study identifier: NCT05690451, KCT0006395), participants who had undergone curative treatment for HCC and remained recurrence-free for over two years were enrolled. Each participant underwent three follow-up imaging sessions at 2–6-month intervals using both CECT and NC-MRI. The primary outcome was the detection accuracy of each modality, analyzed using the generalized estimating equation analysis. Secondary outcomes included sensitivity and specificity.
Results
The study included 203 participants with a total of 528 paired imaging sessions, identifying recurrent HCC in 22 cases (10.8%). Among these, 21 cases involved intrahepatic recurrence with a median tumor size of 1.3 cm, and one case had aortocaval lymph node metastasis. NC-MRI achieved a detection accuracy of 96.6% (196/203), higher than CECT’s 91.6% (186/203) (P=0.006). NC-MRI also showed greater sensitivity (77.3% [17/22] vs. 36.4% [8/22]; P=0.012), while specificity was comparable between NC-MRI and CECT (98.9% [179/181] vs. 98.3% [178/181]; P=0.999).
Conclusions
NC-MRI demonstrated higher sensitivity and accuracy compared to CECT in detecting recurrent HCC in patients who had been disease-free for over two years following curative treatment, indicating its potential as a preferred imaging modality for this purpose.
  • 4,215 View
  • 155 Download

Review

Liver fibrosis, cirrhosis, and portal hypertension

Hepatorenal syndrome: Current concepts and future perspectives
Chan-Young Jung, Jai Won Chang
Clin Mol Hepatol 2023;29(4):891-908.
Published online April 13, 2023
DOI: https://doi.org/10.3350/cmh.2023.0024
Hepatorenal syndrome (HRS), a progressive but potentially reversible deterioration of kidney function, remains a major complication in patients with advanced cirrhosis, often leading to death before liver transplantation (LT). Recent updates in the pathophysiology, definition, and classification of HRS have led to a complete revision of the nomenclature and diagnostic criteria for HRS type 1, which was renamed HRS-acute kidney injury (AKI). HRS is characterized by severe impairment of kidney function due to increased splanchnic blood flow, activation of several vasoconstriction factors, severe vasoconstriction of the renal arteries in the absence of kidney histologic abnormalities, nitric oxide dysfunction, and systemic inflammation. Diagnosis of HRS remains a challenge because of the lack of specific diagnostic biomarkers that accurately distinguishes structural from functional AKI, and mainly involves the differential diagnosis from other forms of AKI, particularly acute tubular necrosis. The optimal treatment of HRS is LT. While awaiting LT, treatment options include vasoconstrictor drugs to counteract splanchnic arterial vasodilation and plasma volume expansion by intravenous albumin infusion. In patients with HRS unresponsive to pharmacological treatment and with conventional indications for kidney replacement therapy (KRT), such as volume overload, uremia, or electrolyte imbalances, KRT may be applied as a bridging therapy to transplantation. Other interventions, such as transjugular intrahepatic portosystemic shunt, and artificial liver support systems have a very limited role in improving outcomes in HRS. Although recently developed novel therapies have potential to improve outcomes of patients with HRS, further studies are warranted to validate the efficacy of these novel agents.

Citations

Citations to this article as recorded by  Crossref logo
  • Paracentesis exceeding three liters increases risks of acute kidney injury even in cirrhotic patients with albumin infused refractory ascites
    Pei-Shan Wu, Kuei-Chuan Lee, Chih-Yu Li, Yun-Cheng Hsieh, Teh-Ia Huo, Han-Chieh Lin, Ming-Chih Hou
    Journal of the Formosan Medical Association.2025;[Epub]     CrossRef
  • Association of visceral fat obesity with structural change in abdominal organs: fully automated three-dimensional volumetric computed tomography measurement using deep learning
    Haruka Kiyoyama, Masahiro Tanabe, Mayumi Higashi, Naohiko Kamamura, Yosuke Kawano, Kenichiro Ihara, Keiko Hideura, Katsuyoshi Ito
    Abdominal Radiology.2025; 50(9): 4395.     CrossRef
  • Understanding and Treating Hepatorenal Syndrome: Insights from Recent Research
    Yuli Song, Xiaochen Yang, Chengbo Yu
    Seminars in Liver Disease.2025; 45(03): 328.     CrossRef
  • Ascites complications risk factors of decompensated cirrhosis patients: logistic regression and prediction model
    Xiaolong Zheng, Wei Wei
    BMC Gastroenterology.2025;[Epub]     CrossRef
  • Emergency living donor liver transplantation
    Jongman Kim
    Annals of Liver Transplantation.2025; 5(1): 27.     CrossRef
  • Assessment of Albumin Therapy and Paracentesis Interval in Cirrhotic Patients With Recurrent Ascites: A Prospective Cohort Study
    Muhammad Abdullah Khan, Hafiz Muhammad Faizan Mughal, Shehwar Ahmed, M Khaliq, Abdul Ghafoor
    Cureus.2025;[Epub]     CrossRef
  • Acute Kidney Injury in Patients with Liver Cirrhosis: From Past to Present Definition and Diagnosis
    Andreea Lungu, Georgiana-Elena Sarbu, Alexandru Sebastian Cotlet, Ilie-Andreas Savin, Ioana-Roxana Damian, Simona Juncu, Cristina Muzica, Irina Girleanu, Ana-Maria Sîngeap, Carol Stanciu, Anca Trifan, Camelia Cojocariu
    Life.2025; 15(8): 1249.     CrossRef
  • Oral Branched-Chain Amino Acids as a Cost-Effective Option for Managing Hepatic Encephalopathy
    Hankil Lee, Sang Hoon Ahn, Beom Kyung Kim
    Yonsei Medical Journal.2025; 66(11): 713.     CrossRef
  • Life after hepatorenal syndrome: unraveling quality of life, psychological distress, and treatment preferences
    J. Müller-Kühnle, M. Schanz, J. Latus, D. Marschner, S. Schricker
    BMC Palliative Care.2025;[Epub]     CrossRef
  • The Kidney in the Shadow of Cirrhosis: A Critical Review of Renal Failure
    Livia-Mirela Popa, Paula Anderco, Oana Stoia, Cristian Ichim, Corina Porr
    Biomedicines.2025; 13(11): 2775.     CrossRef
  • VWF/ADAMTS13 Ratio as a Potential Predictive Biomarker for Acute Kidney Injury Onset in Cirrhosis
    Shohei Asada, Tadashi Namisaki, Kosuke Kaji, Hiroaki Takaya, Takahiro Kubo, Takemi Akahane, Hideto Kawaratani, Norihisa Nishimura, Soichi Takeda, Hiroyuki Masuda, Akihiko Shibamoto, Takashi Inoue, Satoshi Iwai, Fumimasa Tomooka, Yuki Tsuji, Yukihisa Fujin
    Digestive Diseases and Sciences.2024; 69(3): 851.     CrossRef
  • Gut Microbiota and Biomarkers of Endothelial Dysfunction in Cirrhosis
    Irina Efremova, Roman Maslennikov, Elena Poluektova, Oleg Medvedev, Anna Kudryavtseva, George Krasnov, Maria Fedorova, Filipp Romanikhin, Vyacheslav Bakhitov, Salekh Aliev, Natalia Sedova, Tatiana Kuropatkina, Anastasia Ivanova, Maria Zharkova, Ekaterina
    International Journal of Molecular Sciences.2024; 25(4): 1988.     CrossRef
  • Infection-Related Readmissions Are Rising among Patients with Hepatorenal Syndrome: A Nationwide Analysis
    Umer Farooq, Zahid I. Tarar, Ammad J. Chaudhary, Abdallah E. Alayli, Faisal Kamal, Chengdu Niu, Kamran Qureshi
    Livers.2024; 4(2): 268.     CrossRef
  • Management of hepatorenal syndrome and treatment-related adverse events
    Lorenzo Peluso, Marzia Savi, Giacomo Coppalini, Deliana Veliaj, Nicola Villari, Giovanni Albano, Stephen Petrou, Maria C. Pace, Marco Fiore
    Current Medical Research and Opinion.2024; 40(7): 1155.     CrossRef
  • Features of the course of hepatorenal syndrome in decompensated portal hypertension (case report)
    M.I. Tutchenko, D.V. Rudyk, M.S. Besedinskyi, S.L. Chub, Yu.V. Nerushchenko
    GASTROENTEROLOGY.2024; 58(2): 151.     CrossRef
  • Protective effect of long-chain polyunsaturated fatty acids on hepatorenal syndrome in rats
    João Bruno Beretta Duailibe, Cassiana Macagnan Viau, Jenifer Saffi, Sabrina Alves Fernandes, Marilene Porawski
    World Journal of Nephrology.2024;[Epub]     CrossRef
  • Treatment-Related Cost Analysis of Terlipressin for Adults with Hepatorenal Syndrome with Rapid Reduction in Kidney Function
    Xingyue Huang, Jas Bindra, Ishveen Chopra, John Niewoehner, George J. Wan
    Advances in Therapy.2023; 40(12): 5432.     CrossRef
  • 15,141 View
  • 1,451 Download
  • 16 Web of Science
  • Crossref
Case Report

Viral hepatitis

Pure red-cell aplasia and autoimmune hemolytic anemia in a patient with acute hepatitis A
Hyo Jeong Chang, Dong Hyun Sinn, Sung Gyun Cho, Tae Hoon Oh, Tae Joo Jeon, Won Chang Shin, Won Choong Choi
Clin Mol Hepatol 2014;20(2):204-207.
Published online June 30, 2014
DOI: https://doi.org/10.3350/cmh.2014.20.2.204

Pure red cell aplasia (PRCA) and autoimmune hemolytic anemia (AIHA) have rarely been reported as an extrahepatic manifestation of acute hepatitis A (AHA). We report herein a case of AHA complicated by both PRCA and AIHA. A 49-year-old female with a diagnosis of AHA presented with severe anemia (hemoglobin level, 6.9 g/dL) during her clinical course. A diagnostic workup revealed AIHA and PRCA as the cause of the anemia. The patient was treated with an initial transfusion and corticosteroid therapy. Her anemia and liver function test were completely recovered by 9 months after the initial presentation. We review the clinical features and therapeutic strategies for this rare case of extrahepatic manifestation of AHA.

Citations

Citations to this article as recorded by  Crossref logo
  • Case Report: Acute hepatitis A virus infection presenting with direct antiglobulin test-negative autoimmune hemolytic anemia and α-thalassemia trait
    Habiba Debbabi, Eya Chakroun, Hajer Hassine, Hela Kchir, Dhouha Cherif, Haythem Yacoub, Nadia Maamouri
    F1000Research.2025; 13: 1224.     CrossRef
  • Case Report: Acute hepatitis A virus infection presenting with direct antiglobulin test-negative autoimmune hemolytic anemia and α-thalassemia trait
    Habiba Debbabi, Eya Chakroun, Hajer Hassine, Hela Kchir, Dhouha Cherif, Haythem Yacoub, Nadia Maamouri
    F1000Research.2024; 13: 1224.     CrossRef
  • Exacerbation of autoimmune hemolytic anemia associated with pure red cell aplasia after COVID-19: A case report
    Hideo Kimura, Miki Furukawa, Yutaka Shiga, Tatsuyuki Kai, Ikkoh Yasuda, Shungo Katoh, Eiichiro Sando
    Journal of Infection and Chemotherapy.2023; 29(8): 787.     CrossRef
  • Local and systemic autoimmune manifestations linked to hepatitis A infection
    M Doulberis, A Papaefthymiou, S.A. Polyzos, E Vardaka, M Tzitiridou-Chatzopoulou, D Chatzopoulos, A Koffas, V Papadopoulos, F Kyrailidi, J Kountouras
    Acta Gastro Enterologica Belgica.2023; 86(3): 429.     CrossRef
  • Pure red cell aplasia accompanied by COVID-19 successfully treated using cyclosporine
    Susumu Yamazaki, Erika Naito, Ryu Sekiya, Sanehiro Yogi, Kenichiro Komiyama, Yoshitaka Miyakawa, Makoto Nagata
    Journal of Infection and Chemotherapy.2022; 28(2): 304.     CrossRef
  • Hemolytic Anemia after Acute Hepatitis B Virus Infection: A Case Report and Systematic Review
    Takahiro Suzuki, Takeshi Okamoto, Fujimi Kawai, Shuhei Okuyama, Katsuyuki Fukuda
    Internal Medicine.2022; 61(4): 481.     CrossRef
  • Hepatitis A virus infection is complicated by both pancytopenia and autoimmune hemolytic anemia (AIHA)
    Omar Al jandale, Heba Jumah, Hasan Jamil
    Annals of Medicine and Surgery.2022; 78: 103765.     CrossRef
  • Diagnosis and Management of Autoimmune Hemolytic Anemia in Patients with Liver and Bowel Disorders
    Cristiana Bianco, Elena Coluccio, Daniele Prati, Luca Valenti
    Journal of Clinical Medicine.2021; 10(3): 423.     CrossRef
  • Coombs-negative Autoimmune Hemolytic Anemia Followed by Anti-erythropoetin Receptor Antibody-associated Pure Red Cell Aplasia: A Case Report and Review of Literature
    Mayumi Yoshimi, Yutaka Kadowaki, Yuji Kikuchi, Tsuyoshi Takahashi
    Internal Medicine.2016; 55(5): 511.     CrossRef
  • Pure Red Cell Aplasia and Autoimmune Hemolytic Anemia Sequentially Occurring in a Patient with Large Granular T-lymphocytic Leukemia
    Xuemei Qin, Yuan Yu, Shuxin Yan, Ran Wang, Xinguang Liu, Chunyan Chen
    Internal Medicine.2016; 55(11): 1491.     CrossRef
  • 11,293 View
  • 126 Download
  • 8 Web of Science
  • Crossref