Diagnosis of Porphyria after Sternotomy for Severe Calcific Coronary Artery Disease : A Case Report

Fuad M. Al-Azzam, S. Altarabsheh, M. Khasawneh
{"title":"Diagnosis of Porphyria after Sternotomy for Severe Calcific Coronary Artery Disease : A Case Report","authors":"Fuad M. Al-Azzam, S. Altarabsheh, M. Khasawneh","doi":"10.5742/MEIM.2017.92937","DOIUrl":null,"url":null,"abstract":"Acute intermittent porphyria (AIP) is an autosomal disorder marked by a deficiency of the enzyme, the hydroxymethylbilane synthase which is part of the heme biosynthesis. It is manifested clinically by multi-system involvement. Our patient does have chronic ischemic heart disease needed surgical revascularization; his sternotomy incision revealed the classical blackish discoloration of the bone marrow, which guided us for his work up and diagnosis.","PeriodicalId":243742,"journal":{"name":"Middle East Journal of Internal Medicine","volume":"432 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2017-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Middle East Journal of Internal Medicine","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.5742/MEIM.2017.92937","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Acute intermittent porphyria (AIP) is an autosomal disorder marked by a deficiency of the enzyme, the hydroxymethylbilane synthase which is part of the heme biosynthesis. It is manifested clinically by multi-system involvement. Our patient does have chronic ischemic heart disease needed surgical revascularization; his sternotomy incision revealed the classical blackish discoloration of the bone marrow, which guided us for his work up and diagnosis.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
严重钙化性冠状动脉疾病胸骨切开术后卟啉症的诊断1例
急性间歇性卟啉症(AIP)是一种常染色体疾病,其特征是缺乏酶,羟甲基二烷合成酶是血红素生物合成的一部分。临床表现为多系统受累。我们的病人确实患有慢性缺血性心脏病需要手术血运重建术;他的胸骨切口显示了典型的骨髓黑色变色,这指导了我们对他的工作和诊断。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Acute chest syndrome may not have an atherosclerotic background in sickle cell diseases Family opinion regarding their presence with the physicians during active cardio-pulmonary resuscitation of their relatives Frailty : Update on Diagnosis Evaluation and Management Part 2 Parkinson's Disease: An update on Pathophysiology, Epidemiology, Diagnosis and Management Part 5: Management Strategies Small Cell Cancer of the Parotid Gland
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1