• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

一例伴有高度脾肿大的贫血病例。

A Case of Anaemia With High-Grade Splenomegaly.

作者信息

Singh Ranjan K

机构信息

Internal Medicine, Antiretroviral Therapy Centre, District Hospital, Khagaria, IND.

出版信息

Cureus. 2022 May 11;14(5):e24908. doi: 10.7759/cureus.24908. eCollection 2022 May.

DOI:10.7759/cureus.24908
PMID:35706745
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9187194/
Abstract

In tropical areas, there are a variety of parasitic and nonparasitic causes of high-grade splenomegaly. An adolescent male patient with haemoglobin E/β-thalassaemia came with high-grade splenomegaly and severe anaemia, requiring blood transfusions on a regular basis. Treatment with folic acid and antioxidant vitamins reduced the requirement for blood transfusions, brought haemoglobin levels back to near normal, and reduced splenic enlargement.  Haemoglobin E/β-thalassaemia is a haematological condition that causes anaemia and high-grade splenomegaly in the tropics. Initially, the disease was only seen in Southeast Asia, but it has since spread around the world due to migration from that region.

摘要

在热带地区,有多种寄生虫和非寄生虫病因可导致高度脾肿大。一名患有血红蛋白E/β地中海贫血的青少年男性患者出现了高度脾肿大和严重贫血,需要定期输血。使用叶酸和抗氧化维生素进行治疗减少了输血需求,使血红蛋白水平恢复到接近正常,并减轻了脾脏肿大。血红蛋白E/β地中海贫血是一种血液疾病,在热带地区会导致贫血和高度脾肿大。最初,这种疾病仅在东南亚出现,但由于该地区的人口迁移,此后已蔓延至全球。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/55a5/9187194/729ba219386d/cureus-0014-00000024908-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/55a5/9187194/f08622e307c9/cureus-0014-00000024908-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/55a5/9187194/729ba219386d/cureus-0014-00000024908-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/55a5/9187194/f08622e307c9/cureus-0014-00000024908-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/55a5/9187194/729ba219386d/cureus-0014-00000024908-i02.jpg

相似文献

1
A Case of Anaemia With High-Grade Splenomegaly.一例伴有高度脾肿大的贫血病例。
Cureus. 2022 May 11;14(5):e24908. doi: 10.7759/cureus.24908. eCollection 2022 May.
2
Acute splenic sequestration in female children with sickle cell disease in the North of Jordan.约旦北部患有镰状细胞病女童的急性脾滞留
J Trop Pediatr. 2006 Dec;52(6):416-20. doi: 10.1093/tropej/fml042. Epub 2006 Sep 2.
3
The influence of alpha-thalassaemia on the haematological & clinical expression of sickle cell disease in western India.α地中海贫血对印度西部镰状细胞病血液学及临床表型的影响
Indian J Med Res. 1998 Apr;107:178-81.
4
Hyper-reactive malarial splenomegaly (HMS) in a patient with β thalassaemia syndrome.β地中海贫血综合征患者的高反应性疟疾脾肿大(HMS)
Pan Afr Med J. 2014 Nov 21;19:310. doi: 10.11604/pamj.2014.19.310.5576. eCollection 2014.
5
Ultrasonographic assessment of splenic volume at presentation and after anti-malarial therapy in children with malarial anaemia.疟疾性贫血患儿就诊时及抗疟治疗后脾脏体积的超声评估
Malar J. 2015 May 28;14:219. doi: 10.1186/s12936-015-0741-0.
6
Observations on the high foetal haemoglobin gene and its interaction with the thalassaemia gene.关于高胎儿血红蛋白基因及其与地中海贫血基因相互作用的观察
J Clin Pathol. 1962 Jul;15(4):350-6. doi: 10.1136/jcp.15.4.350.
7
The interaction of alpha thalassaemia and sickle cell-beta zero thalassaemia.α地中海贫血与镰状细胞-β0地中海贫血的相互作用。
Br J Haematol. 1988 Dec;70(4):449-54. doi: 10.1111/j.1365-2141.1988.tb02515.x.
8
Ferrokinetic and erythrokinetic studies in alpha and beta thalassaemia.α和β地中海贫血的铁动力学及红细胞动力学研究
Clin Lab Haematol. 1984;6(2):133-40. doi: 10.1111/j.1365-2257.1984.tb00535.x.
9
Sickle cell beta-thalassaemia compared with sickle cell anaemia in Algeria.阿尔及利亚镰状细胞β地中海贫血与镰状细胞贫血的比较。
Scand J Haematol. 1984 Apr;32(4):346-50. doi: 10.1111/j.1600-0609.1984.tb00687.x.
10
Thalassaemia Trait with Gaucher Disease: A Diagnostic Dilemma.地中海贫血特质合并戈谢病:诊断难题
J Clin Diagn Res. 2017 Sep;11(9):ED14-ED15. doi: 10.7860/JCDR/2017/31008.10650. Epub 2017 Sep 1.

本文引用的文献

1
Survival and complications in patients with haemoglobin E thalassaemia in Sri Lanka: a prospective, longitudinal cohort study.斯里兰卡血红蛋白 E 地中海贫血患者的生存和并发症:一项前瞻性、纵向队列研究。
Lancet Glob Health. 2022 Jan;10(1):e134-e141. doi: 10.1016/S2214-109X(21)00446-0. Epub 2021 Nov 26.
2
Clinico-hematological Profile of Hb E-β Thalassemia-Prospective Analysis in a tertiary Care Centre.三级医疗中心血红蛋白E-β地中海贫血的临床血液学特征——前瞻性分析
J Assoc Physicians India. 2018 Jun;66(6):42-45.
3
Treatment of β-Thalassemia/Hemoglobin E with Antioxidant Cocktails Results in Decreased Oxidative Stress, Increased Hemoglobin Concentration, and Improvement of the Hypercoagulable State.
用抗氧化剂鸡尾酒疗法治疗β地中海贫血/血红蛋白E可降低氧化应激、提高血红蛋白浓度并改善高凝状态。
Oxid Med Cell Longev. 2015;2015:537954. doi: 10.1155/2015/537954. Epub 2015 May 19.
4
Ultrasonographic assessment of splenic volume at presentation and after anti-malarial therapy in children with malarial anaemia.疟疾性贫血患儿就诊时及抗疟治疗后脾脏体积的超声评估
Malar J. 2015 May 28;14:219. doi: 10.1186/s12936-015-0741-0.
5
Diagnosis and management of thalassaemia.地中海贫血的诊断与管理
BMJ. 2012 Jan 25;344:e228. doi: 10.1136/bmj.e228.
6
Hb E/beta-thalassaemia: a common & clinically diverse disorder.Hb E/β-地中海贫血:一种常见且临床表现多样的疾病。
Indian J Med Res. 2011 Oct;134(4):522-31.
7
Adaptation to anemia in hemoglobin E-ß thalassemia.血红蛋白 E-β 地中海贫血症的贫血适应。
Blood. 2010 Dec 9;116(24):5368-70. doi: 10.1182/blood-2010-06-289488. Epub 2010 Sep 10.
8
Global epidemiology of haemoglobin disorders and derived service indicators.血红蛋白疾病的全球流行病学及相关服务指标
Bull World Health Organ. 2008 Jun;86(6):480-7. doi: 10.2471/blt.06.036673.
9
A scoring system for the classification of beta-thalassemia/Hb E disease severity.一种用于β地中海贫血/Hb E病严重程度分类的评分系统。
Am J Hematol. 2008 Jun;83(6):482-4. doi: 10.1002/ajh.21130.
10
Beta-thalassemia.β地中海贫血
N Engl J Med. 2005 Sep 15;353(11):1135-46. doi: 10.1056/NEJMra050436.