Wang Wen, Meng Lingbin, Crespo Eric, Adams Jeffrey, Manoucheri Manoucher
Internal Medicine, AdventHealth Orlando, Orlando, USA.
Internal Medicine, AdventHealth Winter Park, Winter Park, USA.
Cureus. 2019 May 14;11(5):e4666. doi: 10.7759/cureus.4666.
Pseudomyxoma peritonei (PMP) is a rare condition that is typically associated with appendicular adenocarcinoma. Other origins are rarely reported. Here, we report a rare case of abdominal PMP, which originated as gastric adenocarcinoma. The prognosis of the patient consisted of pathological diagnosis, with samples from exploratory laparotomy, radiological visualization, abdominal computed tomography (CT), and abdominal magnetic resonance imaging (MRI). We employed the standard treatment protocol for our patient, which was essentially surgical, applying a cytoreductive technique, in an attempt to remove all visible evidence of the disease, plus intraperitoneal chemotherapy.
腹膜假黏液瘤(PMP)是一种罕见疾病,通常与阑尾腺癌相关。其他起源很少有报道。在此,我们报告一例罕见的腹部PMP病例,其起源于胃腺癌。患者的预后包括病理诊断,取材于剖腹探查术、放射影像学检查、腹部计算机断层扫描(CT)和腹部磁共振成像(MRI)。我们对该患者采用了标准治疗方案,主要是手术治疗,应用细胞减灭技术,试图清除所有可见的病灶证据,再加上腹腔内化疗。