急性冠状动脉综合征1例免疫抑制下嗜中性粒细胞还是t细胞犯罪?

IF 0.1 Q4 EMERGENCY MEDICINE Journal of Emergency Medicine Case Reports Pub Date : 2022-10-18 DOI:10.33706/jemcr.1124235
İrem Oktay, Ahmet Lütfü Sertdemir, A. Icli
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引用次数: 0

摘要

慢性肉芽肿病(CGD)是一种原发性免疫缺陷,其特征是皮肤、气道、淋巴结、肝脏、大脑和骨骼的复发性、危及生命的细菌和真菌感染。这些感染最常发生在与外界接触的器官(肺、胃肠道和皮肤),以及排泄这些结构的淋巴结。虽然累及许多器官,但尚未发现累及心血管。我们的病例是一个ACS病例,在文献中有不同的位置,因为急性冠脉综合征(ACS)在一个20岁的男性患者中被诊断为慢性肉芽肿病。
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A CASE OF ACUTE CORONARY SYNDROME UNDER IMMUNSUPRESSION WHO IS THE CRIMINAL NEUTROPHILS OR T CELLS?
Chronic granulomatous disease (CGD) is a primary immunodeficiency characterized by recurrent, life-threatening bacterial and fungal infections of the skin, airways, lymph nodes, liver, brain, and bones. These infections most commonly occur in organs in contact with the outside world (lungs, gastrointestinal tract, and skin), as well as in lymph nodes that drain these structures. While involvement can be seen in many organs, there is no known cardiovascular involvement. Our case is an ACS case that has a different place in the literature because acute coronary syndrome (ACS) was seen in a 20-year-old male patient with a diagnosis of chronic granulomatous disease.
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