Pastor-Navarro Héctor, Broseta-Viana Luis, Donate-Moreno Maria J, Pastor-Guzmán José M, Lorenzo-Romero Juan G, Segura-Martín Miguel, Salinas-Sánchez Antonio S, Virseda-Rodríguez Julio A
Department of Urology, University Hospital Complex of Albacete, Albacete, Spain.
Urology. 2007 Jul;70(1):178.e7-8. doi: 10.1016/j.urology.2007.03.043.
Isolated polyarteritis nodosa is a rare condition that may be triggered by local exposure to certain agents capable of provoking local immunostimulation without a systemic immune reaction. Isolated polyarteritis nodosa in the testes presents similar histologic characteristics as those of systemic inflammation, although infarcted areas in the testis are more common in generalized polyarteritis nodosa. Definitive diagnosis requires histologic study. We present the case of a 26-year-old patient with isolated testicular polyarteritis nodosa whose symptoms consisted predominantly of intense testicular pain and slight enlargement of both testes.
孤立性结节性多动脉炎是一种罕见疾病,可能由局部接触某些能够引发局部免疫刺激而无全身免疫反应的因子所触发。睾丸的孤立性结节性多动脉炎呈现出与全身性炎症相似的组织学特征,尽管在全身性结节性多动脉炎中睾丸梗死区域更为常见。明确诊断需要进行组织学研究。我们报告一例26岁患有孤立性睾丸结节性多动脉炎的患者,其症状主要为剧烈的睾丸疼痛和双侧睾丸轻度肿大。