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200例特发性血小板减少性紫癜的临床分析

[Clinical analysis of 200 cases of idiopathic thrombocytopenic purpura].

作者信息

García-Stivalet Lilia Adela, Muñoz-Flores Aarón, Montiel-Jarquín Alvaro José, Barragán-Hervella Rodolfo Gregorio, Bejarano-Huertas Ruth, García-Carrasco Mario, López-Colombo Aurelio

机构信息

Servicio de Hematología, Hospital General Regional 36, Instituto Mexicano del Seguro Social, Puebla, México.

出版信息

Rev Med Inst Mex Seguro Soc. 2014 May-Jun;52(3):322-5.

Abstract

BACKGROUND

Idiopathic thrombocytopenic purpura is characterized by extravasation of blood into the subcutaneous tissue, mucous membranes or skin; it generates bleeding manifestations as ecchymotic lesions, petechiae of sudden onset, epistaxis, bleeding from the gums, and serious complications such as intracranial hemorrhage. This condition is due to a platelet destruction mediated by antibodies directed against the surface of the platelets. The objective is to present the clinical characteristics of patients with idiopathic thrombocytopenic purpura in a third level medical facility in Puebla, México.

METHODS

A descriptive study, which included 200 patients from the Hematology Service, was carried out. All patients included had the diagnosis of idiopathic thrombocytopenic purpura. We studied their clinical manifestations, type of diagnosis, as well as medical and/or surgical treatment. The statiscal analysis was made using descriptive measures.

RESULTS

The entire sample (200 patients) had idiopathic thrombocytopenic purpura as a diagnosis established, 57 % had ecchymoses, 42 % petechiae, 23 % bleeding from the gums, 31.5 % epistaxis, 6.5 % abnormal uterine bleeding, 11 % malaise, 7.0 % hemorrhage, 0.5 % pruritus, 0.5 % seizures, 8 % two or more signs and symptoms and 73 % was asymptomatic when the diagnosis was established.

CONCLUSIONS

Symptoms of idiopathic thrombocytopenic purpura are varied, a large percentage of patients can be processed unnoticed. The results described were similar to those reported in the literature.

摘要

背景

特发性血小板减少性紫癜的特征是血液渗入皮下组织、黏膜或皮肤;会产生瘀斑、突然出现的瘀点、鼻出血、牙龈出血等出血表现,以及颅内出血等严重并发症。这种情况是由针对血小板表面的抗体介导的血小板破坏所致。目的是呈现墨西哥普埃布拉一家三级医疗机构中特发性血小板减少性紫癜患者的临床特征。

方法

开展了一项描述性研究,纳入了血液科的200名患者。所有纳入患者均诊断为特发性血小板减少性紫癜。我们研究了他们的临床表现、诊断类型以及药物和/或手术治疗情况。使用描述性指标进行统计学分析。

结果

整个样本(200名患者)均确诊为特发性血小板减少性紫癜,57%有瘀斑,42%有瘀点,23%牙龈出血,31.5%鼻出血,6.5%子宫异常出血,11%身体不适,7.0%出血,0.5%瘙痒,0.5%癫痫发作,8%有两种或更多体征和症状,73%在确诊时无症状。

结论

特发性血小板减少性紫癜的症状多样,很大一部分患者在未被注意的情况下得到诊治。所描述的结果与文献报道的相似。

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