Lyu Shaocheng, He Qiang
Department of Hepatobiliary Surgery, Beijing Chaoyang Hospital, Capital Medical University.
J Nippon Med Sch. 2019;86(3):179-182. doi: 10.1272/jnms.JNMS.2019_86-307.
Littoral cell angioma (LCA), a rare vascular neoplasm that occurs in the spleen, is difficult to definitively diagnose preoperatively because histological examination is the only accurate means of diagnosing this condition. Thus, the preoperative diagnosis is often incorrect. Splenectomy is the appropriate treatment and can be performed laparoscopically or by open surgery depending on the size of the tumor. Here we present a case of a 38-year-old man who presented with a history of slight non-specific abdominal distension for 2 months. An abdominal CT scan showed a huge spleen measuring 35×18 cm and containing multiple lesions, the largest being 11.3×9.2 cm. The patient underwent open splenectomy and recovered well. Histological examination showed LCA of the spleen. To our knowledge, this is the largest reported LCA thus far and may advance our understanding of this condition.
脾窦岸细胞血管瘤(LCA)是一种罕见的发生于脾脏的血管肿瘤,术前难以明确诊断,因为组织学检查是诊断此病的唯一准确方法。因此,术前诊断常常有误。脾切除术是合适的治疗方法,可根据肿瘤大小通过腹腔镜或开放手术进行。在此,我们报告一例38岁男性患者,有2个月的轻微非特异性腹胀病史。腹部CT扫描显示脾脏巨大,大小为35×18 cm,内有多个病灶,最大病灶为11.3×9.2 cm。患者接受了开放性脾切除术,恢复良好。组织学检查显示为脾脏LCA。据我们所知,这是迄今为止报道的最大的LCA病例,可能会增进我们对这种疾病的了解。