Department of Surgery, Tokyo Metropolitan Tama Medical Hospital, Fuchu, Tokyo, 183-8524, Japan.
Am J Surg. 2011 Aug;202(2):e17-9. doi: 10.1016/j.amjsurg.2010.10.002.
We herein describe a case of successful surgical treatment of isolated splenic peliosis presenting with giant splenomegaly and severe coagulopathy. Pathological features of the spleen included multinodular, blood-filled, cyst-like lesions distributed throughout the whole organ. The pathogenesis of isolated splenic peliosis is controversial, and no definitive disease mechanism has been reported. To our knowledge, this is the first report in English of a case like this.
我们在此描述了一例成功手术治疗孤立性脾血管瘤的病例，该病例表现为巨大脾肿大和严重凝血功能障碍。脾脏的病理特征包括分布于整个器官的多结节、充满血液的、囊性样病变。孤立性脾血管瘤的发病机制存在争议，目前尚未报道明确的发病机制。据我们所知，这是首例英文报道的此类病例。
