TY -的A2 Tsurumoto t A2 - Madrazo,即非盟- Samona,杰森PY - 2012 DA - 2012/06/28 TI -整形与嗜酸性筋膜炎注意事项:病例报告和文献回顾SP - 865360六世- 2012 AB -嗜酸性筋膜炎(EF)或舒尔曼病是一种非常罕见的疾病在1974年第一次描述了舒尔曼博士在弥散性筋膜炎患者和嗜酸性粒细胞。不到全球已报告300例在过去35年。目前医学界对该病的了解仅依赖于几大系列和多个案件报告。拟议的病因、病理机制和治疗共识是模糊的或缺乏。疾病的表现是可变的,但某些症状和体征与EF。极端罕见的疾病,症状和体征的大星座,以及缺乏知识关于嗜酸性筋膜炎和使这种疾病很难识别和治疗。通过回顾文献,只有一个其他案件由Yamanishi哮喘复发被视为与嗜酸性筋膜炎有关。本文的作者的知识这个病人代表第二个记录事件。本文的作者描述的案例证明了混合单元的初始活检筋膜炎包括嗜酸性粒细胞,相比eosinophil-rich样本在稍后的日期。这可能是一个独特的方面疾病的病理未发现。 Similar scenarios were not noted in a review of the literature. A change in the pathological findings as shown in this case from non-eosinophil-rich sample to one rich in eosinophils is unique in a patient actively suffering from EF. The authors of this paper propose that an allergic reaction (at the patient's puncture site) occurred, which initially caused the left hand symptoms that led to the patient’s first presentation to the hospital. This is a unique causative agent, not found in the review of the literature. Through a review of the literature and the presentation of this patient, the authors propose an underlying dysregulation of the immune system, leading to the initiation or synergistic perpetuation of EF. This is a unique outlook on the disease pathology, not explained much in the medical literature. SN - 2090-6749 UR - https://doi.org/10.1155/2012/865360 DO - 10.1155/2012/865360 JF - Case Reports in Orthopedics PB - Hindawi Publishing Corporation KW - ER -