Department of General Surgery, Institute of Medical Sciences, Banaras Hindu University, Varanasi, India.
Surg Today. 2010;40(2):167-70. doi: 10.1007/s00595-009-4015-8. Epub 2010 Jan 28.
Antiphospholipid syndrome (APS) is a systemic autoimmune disease, which may be primary or secondary to other autoimmune diseases. It produces thrombosis of arteries and veins of any caliber, and no organ is immune to its insult. This report describes two cases of massive gastric gangrene due to primary APS, which presented in a span of 2 years. In the first case a multiparous, 40-year-old woman presented with acute abdominal pain, hematemesis, and progressive abdominal distension, and was in azotemia and shock. A laparotomy revealed gangrene of the stomach without any other organ involvement. She was managed with a total gastrectomy and esophagojejunal anastomosis. Postoperative serology revealed a persistent elevation of anticardiolipin antibody with no other apparent predisposing cause. The histopathological examination of the specimen revealed characteristic extensive intramural vascular thrombosis without inflammatory changes in the vessel wall, confirming antiphospholipid syndrome. The second patient was a primiparous, 26-year-old woman who had severe abdominal pain in the first trimester followed by shock. An exploratory laparotomy revealed massive gangrene of the stomach with complete loss of the posterior wall and hemoperitoneum. She also underwent a total gastrectomy with esophagogastric anastomosis and was later managed in the intensive care unit, where she succumbed within 8 days. Her serology showed a highly elevated anticardiolipin antibody titer, and histopathological examination of the stomach revealed characteristic intramural vascular thrombosis without inflammatory cellular infiltrate in the vessel wall. Patients undergoing a total gastrectomy following acute gastric necrosis have very high mortality (50%-80%). Its association with APS is rare and it has not been previously reported. The combination is a formidable challenge to the physician and a dangerous disease for the patient. The rarity of the condition and its grave prognosis is highlighted.
抗磷脂综合征(APS)是一种系统性自身免疫性疾病,可原发或继发于其他自身免疫性疾病。它可导致任何口径的动静脉血栓形成,没有任何器官能免受其侵害。本报告描述了两例由原发性 APS 引起的巨大胃 gangrene 病例,这两例病例在 2 年内发生。在第一个病例中,一位多产妇,40 岁女性,表现为急性腹痛、呕血和进行性腹胀,并伴有氮质血症和休克。剖腹探查发现胃 gangrene 而无其他器官受累。她接受了全胃切除术和食管空肠吻合术。术后血清学检查显示抗心磷脂抗体持续升高,没有其他明显的潜在病因。标本的组织病理学检查显示特征性的广泛壁内血管血栓形成,而血管壁无炎症改变,证实为抗磷脂综合征。第二个患者是一位初产妇,26 岁女性,在孕早期出现严重腹痛,随后出现休克。剖腹探查发现胃广泛 gangrene,后壁完全丧失,伴血腹。她还接受了全胃切除术和胃食管吻合术,并在重症监护病房接受治疗,8 天后死亡。她的血清学检查显示抗心磷脂抗体滴度显著升高,胃的组织病理学检查显示特征性的壁内血管血栓形成,而血管壁无炎症细胞浸润。急性胃坏死患者行全胃切除术的死亡率非常高(50%-80%)。其与 APS 相关的情况很少见,以前没有报道过。这种组合对医生来说是一个巨大的挑战,对患者来说是一种危险的疾病。这种情况的罕见性及其严重的预后强调了这一点。