Chhaidar Amine, Zouari Skandar, Bdioui Ahlem, Mokni Moncef, Ben Ali Ali
Department of Surgery, Sahloul Hospital, Sousse, Tunisia.
Department of Urology, Sahloul Hospital, Sousse, Tunisia.
Int J Surg Case Rep. 2018;53:127-131. doi: 10.1016/j.ijscr.2018.10.056. Epub 2018 Oct 30.
Hemangiopericytoma is a rare vascular tumor representing about 1% of all vascular tumors and approximatively 5% of all soft tissues sarcomas that arises from the pericytes of Zimmerman surrounding capillaries and postcapillaries vessels. Retroperitoneal hemangiopericytomas are rare among the localisations as it usually occurs in lower and upper extremities.
We present a case of 31-year-old man with a well-defined retro peritoneal mass measuring about 105 × 73 × 83 mm at right lower quadrant of the abdomen anterior to right psoas muscle. Intraoperatively, an large mass measuring 10 × 8 cm was found arising from the retro peritoneum. A monobloc excision was performed. The postoperative course was uneventful. Histopathological examination with immune histochemistry revealed that tumoral cells were positive for desmin, CD34, smooth muscular antigen. Final diagnosis of hemangiopericytoma was made. On the last follow up at one year, he was symptom free.
Hemangiopericytoma is a rare tumor. It takes origin from pericytes presenting as intervals along the walls of capillaries and post-capillary venules. Retroperitoneal hemangiopericytoma is a rare location. It is often discovered at late course, and can be revealed by various symptoms with the compression of the adjacent organs by the tumor Surgical resection should be considered in symptomatic cases or in case of diagnostic dilemma.
Retroperitoneal hemangiopericytoma can be benign but it should be treated the same way as aggressive tumors. It requires a careful and long term follow up.
血管外皮细胞瘤是一种罕见的血管肿瘤,约占所有血管肿瘤的1%,占所有软组织肉瘤的近5%,它起源于围绕毛细血管和毛细血管后小静脉的齐默尔曼周细胞。腹膜后血管外皮细胞瘤在肿瘤发生部位中较为罕见,因为它通常发生在下肢和上肢。
我们报告一例31岁男性患者,在右下腹右腰大肌前方有一个边界清晰的腹膜后肿块,大小约为105×73×83mm。术中发现一个10×8cm的大肿块起源于腹膜后。进行了整块切除。术后过程顺利。组织病理学检查及免疫组化显示肿瘤细胞结蛋白、CD34、平滑肌抗原呈阳性。最终诊断为血管外皮细胞瘤。在最后一次随访(一年时),他无症状。
血管外皮细胞瘤是一种罕见肿瘤。它起源于周细胞,表现为沿毛细血管壁和毛细血管后小静脉壁的节段。腹膜后血管外皮细胞瘤是一个罕见的发病部位。它通常在病程晚期被发现,可因肿瘤压迫相邻器官而出现各种症状。对于有症状的病例或诊断存在困境的情况,应考虑手术切除。
腹膜后血管外皮细胞瘤可以是良性的,但应与侵袭性肿瘤一样进行治疗。它需要仔细且长期的随访。