Pillay Yagan, Shokeir M Omar
Prince Albert Parkland Health Region, Victoria Hospital, 1200-24th Street West, Prince Albert, SK S6V 5T4, Canada.
Int J Surg Case Rep. 2017;40:109-112. doi: 10.1016/j.ijscr.2017.09.017. Epub 2017 Sep 23.
Littoral- cell angioma (LCA) is a rare benign vascular tumour of the spleen. There have been less then 80 cases reported in the literature. Recent reports have described it to be a malignant lesion with congenital and immunologic associations. We report a case of LCA of the spleen.
A 52 -year-old male patient was admitted to hospital with a three month duration of intermittent upper abdominal pain and nausea. Imaging studies, including computer tomography (CT) and magnetic resonance imaging (MRI), showed multiple lesions in the spleen as well as in the accessory spleens. An open splenectomy was performed and his post-operative recovery was uneventful.
Littoral cell angioma of the spleen is a benign vascular tumour that has been infrequently reported in the English literature. While it does have malignant potential, the vast majority are benign. Diagnosis depends on the expression of endothelial markers like CD31 and histiocytic markers like CD68.Malignant potential is enhanced by the presence of splenomegaly as well.
This rare condition is made even more rare by the presence of the tumour in the two accessory spleens as well.
边缘区细胞血管瘤(LCA)是一种罕见的脾脏良性血管肿瘤。文献报道的病例不足80例。最近的报告称其为具有先天性和免疫相关性的恶性病变。我们报告一例脾脏LCA病例。
一名52岁男性患者因间歇性上腹部疼痛和恶心3个月入院。包括计算机断层扫描(CT)和磁共振成像(MRI)在内的影像学检查显示脾脏及副脾有多处病变。行开放性脾切除术,术后恢复顺利。
脾脏边缘区细胞血管瘤是一种良性血管肿瘤,在英文文献中报道较少。虽然它确实有恶变潜能,但绝大多数是良性的。诊断依赖于内皮标志物如CD31和组织细胞标志物如CD68的表达。脾肿大的存在也会增加恶变潜能。
这种罕见疾病因肿瘤同时出现在两个副脾中而变得更加罕见。