Literature DB >> 3348251

Hereditary spherocytosis in the elderly.

E W Friedman1, J C Williams, L Van Hook.   

Abstract

Five patients with hereditary spherocytosis diagnosed in their seventh to ninth decades of life are presented. These patients are remarkable for absent or mild clinical manifestations of disease. Splenectomy is the recommended treatment for hereditary spherocytosis to avoid the complications of aplastic or hemolytic crisis. When the diagnosis is made in the elderly, the treatment of choice may be careful observation with folic acid supplementation rather than splenectomy. This recommendation is based on the incidence of complications of splenectomy in the elderly in comparison to the severity and incidence of complications from the disease itself.

Entities:  

Mesh:

Substances:

Year:  1988        PMID: 3348251     DOI: 10.1016/0002-9343(88)90275-6

Source DB:  PubMed          Journal:  Am J Med        ISSN: 0002-9343            Impact factor:   4.965


  3 in total

1.  Rapid Identification of Biallelic SPTB Mutation in a Neonate with Severe Congenital Hemolytic Anemia and Liver Failure.

Authors:  Christopher M Richmond; Sally Campbell; Hee W Foo; Sebastian Lunke; Zornitza Stark; Amanda Moody; Elizabeth Bannister; Anthea Greenway; Natasha Brown
Journal:  Mol Syndromol       Date:  2020-02-01

2.  Hereditary spherocytosis in a malay patient with chronic haemolysis.

Authors:  Muhammad Kamil Sheikh; Narazah Mohd Yusoff; Gurjeet Kaur; Farhat Aziz Khan
Journal:  Malays J Med Sci       Date:  2007-07

3.  Clinical course of 63 children with hereditary spherocytosis: a retrospective study.

Authors:  Maria Christina Lopes Araujo Oliveira; Rachel Aparecida Ferreira Fernandes; Carolina Lins Rodrigues; Daniela Aguiar Ribeiro; Maria Fernanda Giovanardi; Marcos Borato Viana
Journal:  Rev Bras Hematol Hemoter       Date:  2012
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.