Marano Alessandra, Maione Francesca, Woo Yanghee, Pellegrino Luca, Geretto Paolo, Sasia Diego, Fortunato Mirella, Orcioni Giulio Fraternali, Priotto Roberto, Fasoli Renato, Borghi Felice
Department of Surgery, General and Oncologic Surgery Unit, Santa Croce e Carle Hospital, Cuneo 12100, Italy.
Department of Surgery, City of Hope, Duarte, CA 91010, United States.
World J Clin Cases. 2019 Dec 6;7(23):4011-4019. doi: 10.12998/wjcc.v7.i23.4011.
Perivascular epithelioid cell tumor (PEComa) is a rare mesenchymal neoplasm that can arise in many different organs with a broad spectrum of biological behavior, from indolent to aggressive progression. Only ten cases of gastric PEComas have been reported in the English literature, which were treated with endoscopic, laparoscopic, or open resections. Due to its rarity, the optimal surgical management and prognosis of this tumor are still uncertain.
We present a case of robotic wedge resection of a 6.5 cm bleeding lesion of the gastric fundus located 3 cm below the esophago-gastric junction in a 55-year-old man. Biopsy revealed a malignant tumor with epithelioid cells focally positive for muscle markers desmin and smooth muscle actin. In addition, histology revealed that the tumor was positive for HMB-45, melan-A (MART-1), microphthalmia transcription factor and negative for pan-cytokeratin AE1/AE3, CD34, p40, DOG-1, CD117 (c-kit), S100, CD3, CD79a, caldesmon and myogenin. These markers suggested the possibility of a PEComa. The patient underwent a diagnostic laparoscopy the da Vinci® Si™ system and robotic wedge resection. Final pathology confirmed a malignant gastric PEComa with negative margins. At his 11-mo follow-up visit, the patient remained disease-free.
Gastric PEComa can be treated with a robotic R0 resection with acceptable postoperative and short-term oncological outcomes.
血管周上皮样细胞瘤(PEComa)是一种罕见的间叶性肿瘤,可发生于许多不同器官,其生物学行为谱广泛,从惰性进展到侵袭性进展。英文文献中仅报道了10例胃PEComa病例,这些病例采用了内镜、腹腔镜或开放手术切除治疗。由于其罕见性,该肿瘤的最佳手术治疗方法和预后仍不确定。
我们报告一例55岁男性患者,采用机器人楔形切除术切除位于食管胃交界处下方3 cm处胃底的一个6.5 cm出血性病变。活检显示为恶性肿瘤,上皮样细胞局部表达肌标志物结蛋白和平滑肌肌动蛋白。此外,组织学检查显示肿瘤HMB-45、黑素A(MART-1)、小眼转录因子阳性,而全细胞角蛋白AE1/AE3、CD34、p40、DOG-1、CD117(c-kit)、S100、CD3、CD79a、钙调蛋白和肌细胞生成素阴性。这些标志物提示可能为PEComa。患者使用达芬奇Si™系统进行了诊断性腹腔镜检查及机器人楔形切除术。最终病理证实为恶性胃PEComa,切缘阴性。在11个月的随访中,患者无疾病复发。
胃PEComa可通过机器人R0切除进行治疗,术后及短期肿瘤学结果可接受。