Abosheaishaa Hazem, Rizzo Vincent, Haseeb Ul Rasool Muhammad, Nassar Mahmoud, Elfert Khaled A, Eskaros Saphwat
Internal Medicine, Icahn School of Medicine at Mount Sinai, Queens Hospital Center, New York, USA.
Internal Medicine/Gastroenterology, Cairo University, Cairo, EGY.
Cureus. 2024 Jul 29;16(7):e65666. doi: 10.7759/cureus.65666. eCollection 2024 Jul.
Thrombotic thrombocytopenic purpura (TTP) is a rare, life-threatening hematologic disorder characterized by microangiopathic hemolytic anemia, thrombocytopenia, and organ dysfunction. This report highlights a rare case of small bowel ischemia and ischemic colitis caused by TTP in a 35-year-old woman with systemic lupus erythematosus (SLE), hypertension, and end-stage renal disease on hemodialysis. She presented with severe abdominal pain, diarrhea, vomiting, and bloody bowel movements. Diagnosed through CT, EGD, and colonoscopy and confirmed by ADAMTS13 levels, she was treated with plasma exchange, steroids, and rituximab. After standard therapies failed, resection anastomosis surgery led to clinical improvement. This case underscores the importance of early recognition and treatment of TTP in SLE patients to improve prognosis and reduce morbidity and mortality.
血栓性血小板减少性紫癜(TTP)是一种罕见的、危及生命的血液系统疾病,其特征为微血管病性溶血性贫血、血小板减少和器官功能障碍。本报告重点介绍了一例罕见病例,一名35岁患有系统性红斑狼疮(SLE)、高血压和终末期肾病且正在接受血液透析的女性,因TTP导致小肠缺血和缺血性结肠炎。她出现了严重腹痛、腹泻、呕吐和便血症状。通过CT、上消化道内镜检查(EGD)和结肠镜检查确诊,并经ADAMTS13水平证实,她接受了血浆置换、类固醇和利妥昔单抗治疗。在标准治疗失败后,切除吻合手术使临床症状得到改善。该病例强调了早期识别和治疗SLE患者TTP对于改善预后、降低发病率和死亡率的重要性。