Aetiology of Vascular Purpura in a Single Centre Experience: Contribution of Clinical and Paraclinical Data.

Q4 Medicine
Mediterranean Journal of Rheumatology Pub Date : 2024-01-29 eCollection Date: 2024-03-01 DOI:10.31138/mjr.280723.aov
Amira El Ouni, Faiza Ben Messaoud, Rym Khayati, C Abdelkafi, Zeineb Meddeb, Saloua Hamzaoui, Thara Larbi, Sana Toujani, Kamel Bouslama
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引用次数: 0

Abstract

Background: Vascular purpura can be the clinical expression of infectious, inflammatory, drug-related, neoplastic, and endocrine pathologies. To date, there is no consensus codifying the investigation of vascular purpura, especially when it is isolated.

Patients and methods: We proposed to study through a retrospective study of 73 cases of vascular purpura, occurring during the period 2004-2019 in our internal medicine department, the contribution of various clinical and paraclinical data to the aetiological diagnosis of vascular purpura. Data were considered to be contributory only when they constituted a solid argument in favour of the aetiological diagnosis of vascular purpura.

Results: Our series involved 73 patients including 41 women and 32 men (Gender ratio: 0.78). Mean age was 49 ± 17 years [16-80]. Vascular purpura was isolated in 3% of cases. For the remaining patients, it was associated with functional (91%) or physical (48%) manifestations. It was associated with other skin lesions in 45% of cases. The accepted aetiologies were primary vasculitis (26%), drug-related (15%), infectious (11%) and secondary to connectivitis (10%). No cause was found in a third of cases. Clinical data alone made it possible to suggest the aetiology in more than half of cases. Special investigations were contributory in 46% of cases. The course was contributory in 18% of patients for drug-related and paraneoplastic causes.

Conclusion: vascular purpura's diverse clinical presentation presents diagnostic challenges. Aetiologies include vasculitis, drug reactions, infections, and connective tissue disorders. Comprehensive clinical assessment is essential.

单中心经验中的血管性紫癜病因:临床和辅助临床数据的贡献。
背景:血管性紫癜可能是感染性、炎症性、药物性、肿瘤性和内分泌性疾病的临床表现。迄今为止,尚未就血管性紫癜的调查达成共识,尤其是在孤立的情况下:我们拟通过对 2004-2019 年期间发生在我院内科的 73 例血管性紫癜病例进行回顾性研究,探讨各种临床和辅助临床数据对血管性紫癜病因诊断的贡献。只有当这些数据构成支持血管性紫癜病因诊断的有力论据时,才被认为是有贡献的数据:我们的系列研究涉及 73 名患者,包括 41 名女性和 32 名男性(性别比例:0.78)。平均年龄为 49 ± 17 岁 [16-80]。3%的病例为孤立的血管性紫癜。其余患者则伴有功能性(91%)或躯体性(48%)表现。45%的病例伴有其他皮肤病变。公认的病因是原发性血管炎(26%)、药物相关(15%)、感染(11%)和继发于结缔组织炎(10%)。三分之一的病例找不到病因。半数以上的病例仅凭临床数据就能推断出病因。46%的病例是由于特殊检查造成的。结论:血管性紫癜的临床表现多种多样,给诊断带来了挑战。病因包括血管炎、药物反应、感染和结缔组织疾病。全面的临床评估至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
2.00
自引率
0.00%
发文量
42
审稿时长
8 weeks
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