Literature DB >> 14508799

Hydroxyurea-induced splenic regrowth in an adult patient with severe hemoglobin SC disease.

Yiwu Huang1, Thyagarajan Ananthakrishnan, Joseph E Eid.   

Abstract

Hydroxyurea has been extensively used in patients with sickle cell anemia and severe sickle cell-hemoglobin C (SC) disease to reduce the severity of their diseases. We report here our experience with an adult patient with severe SC disease who developed symptomatic splenomegaly requiring splenectomy while being treated with hydroxyurea. This case suggests that hydroxyurea might restore some splenic function in functionally asplenic patients with sickle cell anemia or SC disease, but also raises the clinical concern that hydroxyurea may induce splenic regrowth, resulting in symptomatic splenomegaly. With the increasing use of hydroxyurea in the management of SS disease or other hemoglobinopathies, the importance of spleen monitoring must be further emphasized in these patients. Copyright 2003 Wiley-Liss Inc.

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Year:  2003        PMID: 14508799     DOI: 10.1002/ajh.10388

Source DB:  PubMed          Journal:  Am J Hematol        ISSN: 0361-8609            Impact factor:   10.047


  5 in total

1.  Long-term hydroxyurea therapy for infants with sickle cell anemia: the HUSOFT extension study.

Authors:  Jane S Hankins; Russell E Ware; Zora R Rogers; Lynn W Wynn; Peter A Lane; J Paul Scott; Winfred C Wang
Journal:  Blood       Date:  2005-10-01       Impact factor: 22.113

Review 2.  Systematic review: Hydroxyurea for the treatment of adults with sickle cell disease.

Authors:  Sophie Lanzkron; John J Strouse; Renee Wilson; Mary Catherine Beach; Carlton Haywood; HaeSong Park; Catherine Witkop; Eric B Bass; Jodi B Segal
Journal:  Ann Intern Med       Date:  2008-05-05       Impact factor: 25.391

Review 3.  Phytomedicines (medicines derived from plants) for sickle cell disease.

Authors:  Oluseyi Oniyangi; Damian H Cohall
Journal:  Cochrane Database Syst Rev       Date:  2018-02-15

4.  Hydroxyurea decreases hospitalizations in pediatric patients with Hb SC and Hb SB+ thalassemia.

Authors:  Jeffrey D Lebensburger; Rakeshkumar J Patel; Prasannalaxmi Palabindela; Christina J Bemrich-Stolz; Thomas H Howard; Lee M Hilliard
Journal:  J Blood Med       Date:  2015-12-15

5.  Phytomedicines (medicines derived from plants) for sickle cell disease.

Authors:  Oluseyi Oniyangi; Damian H Cohall
Journal:  Cochrane Database Syst Rev       Date:  2020-09-25
  5 in total

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