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成人斯蒂尔病

Adult Still's disease.

作者信息

Esdaile J M, Tannenbaum H, Hawkins D

出版信息

Am J Med. 1980 Jun;68(6):825-30. doi: 10.1016/0002-9343(80)90201-6.

Abstract

The clinical and laboratory features in six patients with adult Still's disease are presented and compared with those in 52 other cases gathered from the literature. Although there is no pathognomonic abnormality, the condition can be readily recognized by the striking constellation of clinical and laboratory abnormalities. The typical rash occurs in 90 per cent of the cases, arthritis in 88 per cent, a fever with temperatures of 40 degrees C or more in 83 per cent and leukocytosis of 18,000 cells/mm3 or more in 67 per cent. One or more ot the following are frequently found: lymphadenopathy (48 per cent), splenomegaly (45 per cent), pleuritis or pneumonitis (31 per cent) and pericarditis (26 per cent). The initial therapy of choice is high doses of nonsteroidal anti-inflammatory drugs. This is not an uncommon disease, as was once thought, and awareness of it will avoid unnecessary diagnostic procedures and delay in initiating therapy.

摘要

本文介绍了6例成人斯蒂尔病患者的临床和实验室特征,并与从文献中收集的其他52例病例进行了比较。虽然没有特征性异常,但通过临床和实验室异常的显著组合,该病很容易被识别。典型皮疹见于90%的病例,关节炎见于88%的病例,体温达40℃或更高的发热见于83%的病例,白细胞计数达18,000个/mm3或更高的白细胞增多见于67%的病例。经常发现以下一种或多种情况:淋巴结病(48%)、脾肿大(45%)、胸膜炎或肺炎(31%)和心包炎(26%)。首选的初始治疗方法是大剂量非甾体抗炎药。这并非如人们曾经认为的那样是一种罕见疾病,认识到这一点将避免不必要的诊断程序和治疗延误。

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