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免疫性血小板减少性紫癜作为溃疡性结肠炎患者的一种肠外表现

Immune Thrombocytopenic Purpura as an Extraintestinal Manifestation in a Patient with Ulcerative Colitis.

作者信息

de Medeiros Dutra Renata, Almeida Luciana Rocha, Sinkos Camila, Muraro Bonini Ana Clara, Saad-Hossne Rogerio, Baima Julio Pinheiro, Sassaki Ligia Yukie

机构信息

Medical School, São Paulo State University (Unesp), Botucatu, Brazil.

出版信息

Case Rep Gastroenterol. 2022 Mar 25;16(1):140-147. doi: 10.1159/000522379. eCollection 2022 Jan-Apr.

Abstract

Immune thrombocytopenic purpura (ITP) is characterized by the presence of autoantibodies against platelet membrane antigens, leading to immune-mediated platelet destruction. ITP is considered as a rare extraintestinal manifestation (EIM) of ulcerative colitis (UC). This report aimed to describe a rare case of UC associated with ITP and a review of the literature. A 49-year-old man was admitted to our hospital with severe acute colitis which was responsive to treatment (hydrocortisone 300 mg/day). The patient was discharged from the hospital with prednisone 60 mg/day and azathioprine 50 mg/day. During the follow-up, the dose of azathioprine was increased to 100 mg/day (1.3 mg/kg), while prednisone tapering was started. After 3 months, the patient presented with thrombocytopenia (30,000 platelets/µL) without improvement despite receiving the suspension of azathioprine; thus, a bone marrow aspirate was performed. The bone marrow analysis showed hyperplasia of the erythroid series, megaloblastosis, hyperplasia of megakaryocytes with mild dyspoiesis, and absence of cytotoxicity, a morphological finding consistent with ITP. The patient was treated with prednisone 1 mg/kg/day which resulted in partial improvement of the condition and his still being followed up as outpatient using mesalazine 3.2 g for UC and a platelet count of approximately 50,000/µL using eltrombopag. As reported, ITP is a rare EIM in patients with UC. Due to the risk of complications, such as bleeding, hematological changes in these patients should be considered. The disease should be suspected in the presence of thrombocytopenia, always excluding the side effects of medications in advance, especially immunosuppressants. The correct diagnosis of this rare manifestation and proper treatment are essential to control the condition, prevent complications, and improve the patient's prognosis.

摘要

免疫性血小板减少性紫癜(ITP)的特征是存在针对血小板膜抗原的自身抗体,导致免疫介导的血小板破坏。ITP被认为是溃疡性结肠炎(UC)一种罕见的肠外表现(EIM)。本报告旨在描述1例罕见的UC合并ITP病例并进行文献复习。一名49岁男性因严重急性结肠炎入院,对治疗(氢化可的松300mg/天)有反应。患者出院时服用泼尼松60mg/天和硫唑嘌呤50mg/天。在随访期间,硫唑嘌呤剂量增加至100mg/天(1.3mg/kg),同时开始逐渐减少泼尼松剂量。3个月后,患者出现血小板减少(血小板计数30,000/µL),尽管停用了硫唑嘌呤但仍无改善;因此,进行了骨髓穿刺。骨髓分析显示红系增生、巨幼样变、巨核细胞增生伴轻度发育异常,且无细胞毒性,这一形态学表现与ITP一致。患者接受泼尼松1mg/kg/天治疗,病情部分改善,目前仍作为门诊患者随访,使用美沙拉嗪3.2g治疗UC,使用艾曲泊帕使血小板计数维持在约50,000/µL。据报道,ITP是UC患者中一种罕见的EIM。由于存在出血等并发症风险,应考虑这些患者的血液学变化。在出现血小板减少时应怀疑该病,始终要提前排除药物副作用,尤其是免疫抑制剂的副作用。正确诊断这种罕见表现并进行恰当治疗对于控制病情、预防并发症及改善患者预后至关重要。

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