Mizuta Yohei, Isomoto Hajime, Kadokawa Yoshiko, Akazawa Yuko, Chin Shunzen, Kanazawa Yusei, Takeshima Fuminao, Omagari Katsuhisa, Murase Kunihiko, Sawai Terumitsu, Nakagoe Tohru, Murata Ikuo, Kohno Shigeru
Second Department of Internal Medicine, Nagasaki University School of Medicine, 1-7-1 Sakamoto, Nagasaki 852-8501, Japan.
J Gastroenterol. 2003;38(9):884-90. doi: 10.1007/s00535-002-1166-4.
Extraintestinal manifestations of ulcerative colitis (UC) are well known, but immunologically mediated hematological diseases are relatively rare. We describe two cases of immune thrombocytopenic purpura (ITP) associated with preexisting UC. Our patients had typical symptoms of UC, and endoscopy showed pancolitis. During treatment with 5-aminosalicylic acid and steroids, severe thrombocytopenia was noted. ITP was diagnosed based on a normal to high number of megakaryocytes in the bone marrow, positive autoantibody to platelet membrane antigen, and absence of splenomegaly. Medical treatment, including increased dosage of steroids, failed to control UC and ITP in both patients. In the first patient, the platelet count recovered after colectomy, while the second patient died of a cerebral hemorrhage. We stress that a diagnosis of ITP should be considered for thrombocytopenia in patients with UC, especially those showing extensive and significant colonic inflammation, and that colectomy of UC might resolve resistant ITP.
溃疡性结肠炎(UC)的肠外表现已为人熟知,但免疫介导的血液系统疾病相对少见。我们描述了两例与既往存在的UC相关的免疫性血小板减少性紫癜(ITP)病例。我们的患者有UC的典型症状,内镜检查显示全结肠炎。在使用5-氨基水杨酸和类固醇治疗期间,发现严重血小板减少。ITP的诊断基于骨髓中巨核细胞数量正常至高、血小板膜抗原自身抗体阳性以及无脾肿大。包括增加类固醇剂量在内的药物治疗未能控制两名患者的UC和ITP。在第一名患者中,结肠切除术后血小板计数恢复,而第二名患者死于脑出血。我们强调,对于UC患者出现的血小板减少,尤其是那些表现为广泛且严重结肠炎症的患者,应考虑诊断为ITP,并且UC的结肠切除术可能会缓解难治性ITP。