Haemorrhagic Lupus: A Diagnosis Emergency, Report about 6 Cases

Fall Biram Codou, W. Dimitri, Dieng Mouhamed, Diaw Bamba, Tode Johanita, Gaye Ahmadou, Salane Aly, N. Cheikh, Cisse Amadou Fall, Sow Maimouna, M. Ndour, Djiba Boundia, Kane Baïdy Sy, F. Seynabou, L. Abdoulaye, Pouye Abdoulaye, Ndongo Souhaibou
{"title":"Haemorrhagic Lupus: A Diagnosis Emergency, Report about 6 Cases","authors":"Fall Biram Codou, W. Dimitri, Dieng Mouhamed, Diaw Bamba, Tode Johanita, Gaye Ahmadou, Salane Aly, N. Cheikh, Cisse Amadou Fall, Sow Maimouna, M. Ndour, Djiba Boundia, Kane Baïdy Sy, F. Seynabou, L. Abdoulaye, Pouye Abdoulaye, Ndongo Souhaibou","doi":"10.4236/ojim.2021.114019","DOIUrl":null,"url":null,"abstract":"Introduction: Haemorrhagic manifestations rarely represent the mode of onset of lupus and are a therapeutical and diagnosis emergency. We report 6 cases of haemorrhagic manifestations disclosing lupus. Patients and methods: It’s about a retrospective, descriptive and multicentric study ranged from 1st January 2014 to 5th January 2019. Were included in the study all cases of lupic disease revealed by hemorrhagic disorders, recorded in 3 Internal Medicine Departments in Dakar: DalalJamm, Dantec, Pikine. The diagnosis of lupus was made on the basis of the 1997 modified classification criteria of ACR for SLE. Results: We gathered 6 cases of women affected by lupic disease. The mean age was 32 years old with extremes ranged from 17 to 56 years. According to haemorrhagic disorders, the diagnosis of lupus was automatically made in 5 of the cases and it took 6 to confirm the last one. Haemorrhagic features were ruled by purpura (3/6 cases) and nosebleeding associated with gumbleeding (2/6 cases), epistaxis and melena (1/6 case), hypermenorrhea (1/6 case), cerebral haematoma (1/6case). Cutaneous (5/6), articular (4/6), renal (2/6) and serous (2/6) disorders specially represented the other manifestations. Biological findings showed cytopenia with 3 cases of anaemia, 1 case of leucopenia and 6 cases of thrombopenia. The average of the platelet count was at 20,000 cells/mm 3 with extremes ranged from 1000 to 35,000 cells/mm 3 . Thrombocytopenia was related to autoimmune thrombocytopenic purpura in 3 cases, to Evans’ syndrome in 2 cases, to macrophage activation syndrome in 1 Immunological investigations found the presence of antinuclear antibodies anti-dsDNA and anti-Sm All received bolus administration Prednisone at a of 1.5 mg/kg (3 cases) and 1 mg/kg to the other patients. A transfusion of platelet concentrates was performed for all of them. The evolution was favorable in 4 cases. Two patients died according to a septic and haemorrhagic shock. Conclusion: We report 6 cases of haemorrhagic manifestations disclosing lupus. Cutaneo-mucous location was more frequent and was related to moderate to severe thrombocytopenia with the presence of anti-Sm antibodies.","PeriodicalId":60567,"journal":{"name":"内科学期刊(英文)","volume":"1 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2021-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"内科学期刊(英文)","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.4236/ojim.2021.114019","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

Introduction: Haemorrhagic manifestations rarely represent the mode of onset of lupus and are a therapeutical and diagnosis emergency. We report 6 cases of haemorrhagic manifestations disclosing lupus. Patients and methods: It’s about a retrospective, descriptive and multicentric study ranged from 1st January 2014 to 5th January 2019. Were included in the study all cases of lupic disease revealed by hemorrhagic disorders, recorded in 3 Internal Medicine Departments in Dakar: DalalJamm, Dantec, Pikine. The diagnosis of lupus was made on the basis of the 1997 modified classification criteria of ACR for SLE. Results: We gathered 6 cases of women affected by lupic disease. The mean age was 32 years old with extremes ranged from 17 to 56 years. According to haemorrhagic disorders, the diagnosis of lupus was automatically made in 5 of the cases and it took 6 to confirm the last one. Haemorrhagic features were ruled by purpura (3/6 cases) and nosebleeding associated with gumbleeding (2/6 cases), epistaxis and melena (1/6 case), hypermenorrhea (1/6 case), cerebral haematoma (1/6case). Cutaneous (5/6), articular (4/6), renal (2/6) and serous (2/6) disorders specially represented the other manifestations. Biological findings showed cytopenia with 3 cases of anaemia, 1 case of leucopenia and 6 cases of thrombopenia. The average of the platelet count was at 20,000 cells/mm 3 with extremes ranged from 1000 to 35,000 cells/mm 3 . Thrombocytopenia was related to autoimmune thrombocytopenic purpura in 3 cases, to Evans’ syndrome in 2 cases, to macrophage activation syndrome in 1 Immunological investigations found the presence of antinuclear antibodies anti-dsDNA and anti-Sm All received bolus administration Prednisone at a of 1.5 mg/kg (3 cases) and 1 mg/kg to the other patients. A transfusion of platelet concentrates was performed for all of them. The evolution was favorable in 4 cases. Two patients died according to a septic and haemorrhagic shock. Conclusion: We report 6 cases of haemorrhagic manifestations disclosing lupus. Cutaneo-mucous location was more frequent and was related to moderate to severe thrombocytopenia with the presence of anti-Sm antibodies.
出血性狼疮急诊诊断报告6例
简介:出血表现很少代表狼疮的发作模式,是治疗和诊断的紧急情况。我们报告6例狼疮的出血表现。患者和方法:这是一项回顾性、描述性和多中心研究,研究时间为2014年1月1日至2019年1月5日。研究纳入了达喀尔3个内科:DalalJamm、Dantec、Pikine记录的所有由出血性疾病显示的狼疮病病例。狼疮的诊断是根据1997年修订的SLE ACR分类标准。结果:我们收集了6例女性狼疮患者。平均年龄32岁,极值为17 ~ 56岁。根据出血性疾病,5例自动诊断为狼疮,最后一例确诊用时6次。出血特征以紫癜(3/6)、鼻出血合并牙龈出血(2/6)、鼻出血合并黑痘(1/6)、月经过多(1/6)、脑血肿(1/6)为主。皮肤(5/6),关节(4/6),肾脏(2/6)和浆液(2/6)疾病特别代表其他表现。生物学表现为细胞减少,其中贫血3例,白细胞减少1例,血小板减少6例。血小板计数的平均值为20,000个细胞/mm 3,极值范围为1,000至35,000个细胞/mm 3。血小板减少症与自身免疫性血小板减少性紫癜3例,与Evans综合征2例,与巨噬细胞活化综合征1例有关。免疫学检查发现抗核抗体-抗dsdna和抗sm存在。所有患者均输注血小板浓缩物。4例进化有利。两名患者死于败血症和出血性休克。结论:我们报告6例狼疮的出血表现。皮肤-粘膜部位更常见,与存在抗sm抗体的中度至重度血小板减少症有关。
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 求助全文
来源期刊
自引率
0.00%
发文量
217
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信
小红书