Putterman C, Barak V, Caraco Y, Neuman T, Shalit M
Department of Oncology, Hadassah University Medical Center, Jerusalem, Israel.
Ann Allergy. 1993 Mar;70(3):243-8.
Episodic angioedema with eosinophilia is a rare syndrome, characterized by periodic attacks of fever, myalgia, angioedema, and oliguria, associated with an increased eosinophil count. The pathogenesis of this disorder is incompletely understood. We describe an additional patient with episodic angioedema and eosinophilia, and review the literature regarding the clinical features and treatment of this disease. Previous hypotheses regarding disease mechanisms are discussed. In our patient, we found high basal levels of interleukin-1 (IL-1) and soluble interleukin-2 receptor (sIL-2R), with further increases in levels of both mediators during attacks. We suggest that IL-1 and T cell activation may play a role in the pathophysiology of episodic angioedema with eosinophilia.
伴嗜酸性粒细胞增多的发作性血管性水肿是一种罕见综合征,其特征为发热、肌痛、血管性水肿和少尿的周期性发作,并伴有嗜酸性粒细胞计数增加。这种疾病的发病机制尚未完全明确。我们描述了另外一例伴发作性血管性水肿和嗜酸性粒细胞增多的患者,并回顾了关于该疾病临床特征和治疗的文献。讨论了以往关于疾病机制的假说。在我们的患者中,我们发现白细胞介素-1(IL-1)和可溶性白细胞介素-2受体(sIL-2R)的基础水平较高,且在发作期间这两种介质的水平进一步升高。我们认为IL-1和T细胞激活可能在伴嗜酸性粒细胞增多的发作性血管性水肿的病理生理学中起作用。