• 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

长期使用粒细胞集落刺激因子(G-CSF)治疗严重先天性中性粒细胞减少症所导致的“头发直立”颅骨表现。

"Hair-on-end" skull induced by long-term G-CSF treatment in severe congenital neutropenia.

作者信息

Albert Michael H, Notheis Gundula, Wintergerst Uwe, Born Christine, Schneider Karl

机构信息

Department of Haematology/Oncology, Dr. von Haunersches Kinderspital, Lindwurmstrasse 4, 80337 Munich, Germany.

出版信息

Pediatr Radiol. 2007 Feb;37(2):221-4. doi: 10.1007/s00247-006-0363-3. Epub 2006 Dec 21.

DOI:10.1007/s00247-006-0363-3
PMID:17186232
Abstract

"Hair-on-end" skull changes are typically seen in individuals suffering from thalassaemia. They are induced by widening of the diploic space due to marrow expansion that is a consequence of ineffective and excessive erythropoiesis. We present a child with severe congenital neutropenia who exhibited the typical hair-on-end sign on plain skull radiographs and MRI. In this patient the skull changes were very likely induced by the expansion of white blood cell precursors induced by long-term daily injections of recombinant human granulocyte colony stimulating factor (G-CSF) to treat his confounding disease. This case report is the first description of hair-on-end changes associated with the use of G-CSF.

摘要

“头发直立”颅骨改变通常见于患有地中海贫血的个体。它们是由骨髓扩张导致的板障间隙增宽引起的,而骨髓扩张是无效和过度红细胞生成的结果。我们报告一名患有严重先天性中性粒细胞减少症的儿童,其在颅骨平片和磁共振成像(MRI)上表现出典型的“头发直立”征象。在该患者中,颅骨改变很可能是由于长期每日注射重组人粒细胞集落刺激因子(G-CSF)以治疗其复杂疾病所导致的白细胞前体扩张引起的。本病例报告是首次描述与使用G-CSF相关的“头发直立”改变。

相似文献

1
"Hair-on-end" skull induced by long-term G-CSF treatment in severe congenital neutropenia.长期使用粒细胞集落刺激因子(G-CSF)治疗严重先天性中性粒细胞减少症所导致的“头发直立”颅骨表现。
Pediatr Radiol. 2007 Feb;37(2):221-4. doi: 10.1007/s00247-006-0363-3. Epub 2006 Dec 21.
2
Osteoporosis in severe congenital neutropenia: inherent to the disease or a sequela of G-CSF treatment?严重先天性中性粒细胞减少症中的骨质疏松症:是疾病固有特征还是粒细胞集落刺激因子治疗的后遗症?
Am J Hematol. 1996 Jun;52(2):127. doi: 10.1002/(SICI)1096-8652(199606)52:2<127::AID-AJH17>3.0.CO;2-E.
3
Osteoporosis in severe congenital neutropenia treated with granulocyte colony-stimulating factor.接受粒细胞集落刺激因子治疗的严重先天性中性粒细胞减少症患者的骨质疏松症。
Br J Haematol. 1995 Apr;89(4):927-8. doi: 10.1111/j.1365-2141.1995.tb08441.x.
4
MPGN type I induced by granulocyte colony stimulating factor.粒细胞集落刺激因子诱导的I型膜增生性肾小球肾炎
Pediatr Nephrol. 2002 May;17(5):370-2. doi: 10.1007/s00467-002-0847-9.
5
Malignant myeloid transformation in congenital forms of neutropenia.先天性中性粒细胞减少症的恶性髓系转化
Isr Med Assoc J. 2002 Nov;4(11):1011-4.
6
Trisomy 21 and isodicentric chromosome 21 in Kostmann syndrome following treatment with G-CSF.使用粒细胞集落刺激因子(G-CSF)治疗后,科斯特曼综合征患者出现21三体和等臂双着丝粒21号染色体。
Cancer Genet Cytogenet. 2001 Apr 1;126(1):78-80. doi: 10.1016/s0165-4608(00)00393-9.
7
Bullous Sweet's syndrome after granulocyte colony-stimulating factor therapy in a child with congenital neutropenia.先天性中性粒细胞减少症患儿接受粒细胞集落刺激因子治疗后发生大疱性Sweet综合征。
Pediatr Dermatol. 2014 Mar-Apr;31(2):e61-2. doi: 10.1111/pde.12282. Epub 2014 Jan 5.
8
Effects of a formulary change from granulocyte colony-stimulating factor to granulocyte-macrophage colony-stimulating factor on outcomes in patients treated with myelosuppressive chemotherapy.从粒细胞集落刺激因子改为粒细胞-巨噬细胞集落刺激因子的处方变更对接受骨髓抑制性化疗患者结局的影响。
Pharmacotherapy. 2005 Mar;25(3):372-8. doi: 10.1592/phco.25.3.372.61608.
9
Leukocytoclastic vasculitis in patients with severe congenital neutropenia.严重先天性中性粒细胞减少症患者的白细胞碎裂性血管炎。
J Trop Pediatr. 2010 Oct;56(5):359-62. doi: 10.1093/tropej/fmp140. Epub 2010 Jan 25.
10
Mutations in the gene for the granulocyte colony-stimulating-factor receptor in patients with acute myeloid leukemia preceded by severe congenital neutropenia.急性髓系白血病患者中粒细胞集落刺激因子受体基因的突变发生在严重先天性中性粒细胞减少症之前。
N Engl J Med. 1995 Aug 24;333(8):487-93. doi: 10.1056/NEJM199508243330804.

引用本文的文献

1
Hair-on-End Sign in a 9-Year-Old Girl Presenting with Acute Stroke in Sickle Cell Disease.镰状细胞病伴急性卒中的9岁女孩的毛糙骨征
Int Med Case Rep J. 2022 Feb 24;15:69-73. doi: 10.2147/IMCRJ.S345847. eCollection 2022.

本文引用的文献

1
The incidence of leukemia and mortality from sepsis in patients with severe congenital neutropenia receiving long-term G-CSF therapy.接受长期粒细胞集落刺激因子(G-CSF)治疗的严重先天性中性粒细胞减少症患者的白血病发病率和败血症死亡率。
Blood. 2006 Jun 15;107(12):4628-35. doi: 10.1182/blood-2005-11-4370. Epub 2006 Feb 23.
2
'Hair-on-end' skull changes resembling thalassemia caused by marrow expansion in uncorrected complex cyanotic heart disease.未经矫正的复杂性青紫型心脏病中,由于骨髓扩张导致类似地中海贫血的“头发直立”颅骨改变。
Pediatr Radiol. 2005 Jul;35(7):698-701. doi: 10.1007/s00247-005-1403-0. Epub 2005 Mar 18.
3
Risk and benefit of treatment of severe chronic neutropenia with granulocyte colony-stimulating factor.
使用粒细胞集落刺激因子治疗严重慢性中性粒细胞减少症的风险与益处。
Semin Hematol. 2002 Apr;39(2):134-40. doi: 10.1053/shem.2002.31914.
4
Kostmann syndrome and severe congenital neutropenia.科斯特曼综合征和严重先天性中性粒细胞减少症。
Semin Hematol. 2002 Apr;39(2):82-8. doi: 10.1053/shem.2002.31913.
5
The hair-on-end sign.毛刺征。
Radiology. 2001 Nov;221(2):347-8. doi: 10.1148/radiol.2212991231.
6
Mutations in the gene encoding neutrophil elastase in congenital and cyclic neutropenia.先天性和周期性中性粒细胞减少症中编码中性粒细胞弹性蛋白酶的基因突变。
Blood. 2000 Oct 1;96(7):2317-22.
7
Active bone marrow distribution as a function of age in humans.
Phys Med Biol. 1981 May;26(3):389-400. doi: 10.1088/0031-9155/26/3/003.
8
Skeletal changes in the anemias.贫血中的骨骼变化。
Semin Roentgenol. 1974 Jul;9(3):169-84. doi: 10.1016/0037-198x(74)90015-7.
9
The "lamellated" skull in beta-thalassaemia.β地中海贫血中的“板层状”颅骨。
Skeletal Radiol. 1989;18(5):373-6. doi: 10.1007/BF00361428.
10
Lamellation of the diploe in the skulls of patients with sickle cell anaemia.镰状细胞贫血患者颅骨板障的分层现象。
Arch Dis Child. 1975 Dec;50(12):948-52. doi: 10.1136/adc.50.12.948.