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Scandinavian Journal of Gastroenterology Volume 42, 2007 - Issue 4
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ORIGINAL ARTICLE

Liver involvement in acute vaso-occlusive crisis of sickle cell disease: Prevalence and predisposing factors

John Koskinas Academic Department of Medicine, Hippokration General Hospital, Athens, Greece
,
Emanuel K. Manesis Academic Department of Medicine, Hippokration General Hospital, Athens, GreeceCorrespondence[email protected]
, MD,
George H. Zacharakis Academic Department of Medicine, Hippokration General Hospital, Athens, Greece
,
Nikolaos Galiatsatos Biochemical Laboratory, Hippokration General Hospital, Athens, Greece
,
Nikolaos Sevastos Academic Department of Medicine, Hippokration General Hospital, Athens, Greece
&
Athanasios J. Archimandritis Academic Department of Medicine, Hippokration General Hospital, Athens, Greece
Pages 499-507 | Received 30 Jun 2006, Published online: 08 Jul 2009

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Harsha Lad, Shoma Naskar, S. K. D. B. Punyasri Pasupuleti, Rakesh Nahrel, Pradeep Sihare, Giriraj R. Chandak & Pradeep K. Patra. (2023) Evaluation of pharmacological efficacy and safety of hydroxyurea in sickle cell disease: Study of a pediatric cohort from Chhattisgarh, India. Pediatric Hematology and Oncology 40:4, pages 395-406.
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Konstantinos Manganas, Sophia Delicou, Aikaterini Xydaki & John Koskinas. (2022) Iron Chelators, Such as Deferasirox, When Combined With Hydroxyurea, Provide an Additional Benefit of Iron Chelation in Patients Receiving Chronic Transfusion Therapy. Hemoglobin 46:2, pages 114-117.
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Articles from other publishers (18)

Govind Choudhary, Nida Mirza & Swati Patel. (2024) Secondary hemophagocytic lymphohistiocytosis in a child with Sickle Cell Anemia and Hepatitis A and Hepatitis E co-infection: A case report. Pediatric Hematology Oncology Journal 9:1, pages 28-31.
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Pari Jafari, Gertruda Evaristo, Xiaotang Alison Du, Aarti E. Sharma, Victoria Marcus, Xiuli Liu, Lei Zhao, Maria Westerhoff & John Hart. (2024) Portosinusoidal Vascular Disorder: A Heretofore Unrecognized Manifestation of Sickle Cell Disease?. Modern Pathology 37:1, pages 100351.
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Srinivas Srinidhi Vadlapudi, Anshu Srivastava, Praveer Rai, Rajneesh K. Singh, Moinak Sen Sarma, Ujjal Poddar & Rajanikant R. Yadav. (2023) Jaundice in a Child with Sickle Cell Anemia: A Case Based Approach. Indian Journal of Pediatrics 91:1, pages 73-80.
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Xu Zhang, Jin Han, Binal N. Shah, Santosh L. Saraf & Victor R. Gordeuk. (2023) Platelet count decline and high neutrophil count within the first day of admission for painful sickle cell vaso‐occlusive episodes predict severe complications. British Journal of Haematology 202:3.
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Omer Saeed, Nicole Panarelli, Kavita Umrau, Hwajeong Lee, Maria Westerhoff, Jerome Cheng & Jingmei Lin. (2022) The Histopathologic Features of Sickle Cell Hepatopathy: A Multi-Institutional Study. American Journal of Clinical Pathology 157:1, pages 73-81.
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Kathleen M. Campbell. 2021. Liver Disease in Children. Liver Disease in Children 730 748 .
Dibya L. Praharaj & Anil C. Anand. (2021) Sickle Hepatopathy. Journal of Clinical and Experimental Hepatology 11:1, pages 82-96.
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Mariangela Giunta & Mirella Fraquelli. 2021. Elastography of the Liver and Beyond. Elastography of the Liver and Beyond 257 268 .
Sree Karthik Pratapa, Sourya Acharya, Yash Gupte & Samarth Shukla. (2020) Acute B Virus Hepatitis with Fulminant Hepatic Failure Precipitating Crisis in Sickle Cell Disease. Journal of Evolution of Medical and Dental Sciences 9:03, pages 173-175.
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Joseph Runde & Ruba K. Azzam. (2018) Hepatobiliary Manifestations in Systemic Disease. Pediatric Annals 47:11.
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Dalia A. Saied, Mona S. El-Raziky, Mona K. El-Ghamrawy & Marwa A. Mahmoud. (2017) The pattern of hepatobiliary complications among Egyptian sickle cell disease children. Egyptian Pediatric Association Gazette 65:2, pages 54-59.
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Danilo Grünig Humberto da Silva, Edis Belini Junior, Lidiane de Souza Torres, Jessika Viviani Okumura, Willian Marcel Barberino, Renan Garcia de Oliveira, Vanessa Urbinatti Teixeira, Clarisse Lopes de Castro Lobo, Eduardo Alves de Almeida & Claudia Regina Bonini-Domingos. (2017) Impact of genetic polymorphisms in key enzymes of homocysteine metabolism on the pathophysiology of sickle cell anemia. Free Radical Biology and Medicine 106, pages 53-61.
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Carly S. Gardner, Daniel T. Boll, Priya Bhosale & Tracy A. Jaffe. (2016) CT abdominal imaging findings in patients with sickle cell disease: acute vaso-occlusive crisis, complications, and chronic sequelae. Abdominal Radiology 41:12, pages 2524-2532.
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Eran Israeli & Charles N. Bernstein. 2015. Yamada' s Textbook of Gastroenterology. Yamada' s Textbook of Gastroenterology 2399 2439 .
Kathleen M. Campbell. 2014. Liver Disease in Children. Liver Disease in Children 694 709 .
Christopher Koh, Tiffany Turner, Xiongce Zhao, Caterina P. Minniti, Jordan J. Feld, Jennifer Simpson, Mary Demino, Anna K. Conrey, Mary J. Jackson, Catherine Seamon, David E. Kleiner, Gregory J. Kato & Theo Heller. (2013) Liver stiffness increases acutely during sickle cell vaso‐occlusive crisis. American Journal of Hematology 88:11.
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Ellen C. Ebert, Michael Nagar & Klaus D. Hagspiel. (2010) Gastrointestinal and Hepatic Complications of Sickle Cell Disease. Clinical Gastroenterology and Hepatology 8:6, pages 483-489.
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Ersi VoskaridouDimitrios ChristoulasAntonios BilalisEleni PlataKonstantinos VarvagiannisGeorge Stamatopoulos, Klio SinopoulouAggeliki BalassopoulouDimitris Loukopoulos & Evangelos Terpos. (2010) The effect of prolonged administration of hydroxyurea on morbidity and mortality in adult patients with sickle cell syndromes: results of a 17-year, single-center trial (LaSHS). Blood 115:12, pages 2354-2363.
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