溃疡性结肠炎、遗传性血栓形成倾向和冠状病毒感染是连锁的:12岁女孩合并症的临床病例

E. Fedulova, A. I. Khavkin, G.V. Medyansteva, V.A. Tsaryev
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引用次数: 0

摘要

我们报告一名12岁女孩急性溃疡性结肠炎(UC)的临床病例,临床表现为大便带血,遗传性血栓形成,表现为左下肢静脉血栓性改变,临床上我们面临左腿肿胀。结肠镜及活检组织学检查证实大肠黏膜病理改变,腹部器官增强CT及下肢超声检查发现静脉血栓形成。这个临床病例的复杂性是由于UC的血栓性并发症和遗传性血栓性疾病难以鉴别诊断。血栓形成的主要治疗方法导致UC血液学表现加重的高风险,这需要长期选择合适的治疗方法,使血栓块溶解而不产生胃肠道出血。在磺胺氮嗪联合肝素治疗的背景下,患者病情明显改善。关键词:遗传性血栓,肝素,结肠镜检查,磺胺氮嗪,血栓形成,溃疡性结肠炎
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Ulcerative colitis, hereditary thrombophilia and coronavirus infection as links in a chain: the clinical case of comorbidity in 12-year-old girl
We present the clinical case of a 12-year-old girl with acute ulcerative colitis (UC), which was clinically manifested by blood in the stool, and genetic thrombophilia, which in turn was manifested by thrombotic changes in the veins of the left lower limb and clinically we faced with the swelling of the left leg. At the colonoscopy and histological examination of biopsies we established the pathological changes in the mucous membrane of the large intestine, on CT of the abdominal organs with contrast enhancement and ultrasound of the lower extremities found the venous thrombosis. The complexity of this clinical case is due to the difficulty of differential diagnosis of thrombotic complications of UC and hereditary thrombophilia.The main therapy for thrombosis causes a high risk of aggravation of hematological manifestations of UC, which required a long-term selection of suitable therapy that allowed the thrombotic masses to dissolve without gastrointestinal bleeding. The condition of patient was improved significantly against the background of therapy with sulfasalazine and heparin. Key words: genetic thrombophilia, heparin, colonoscopy, sulfasalazine, thrombosis, ulcerative colitis
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来源期刊
Voprosy Prakticheskoi Pediatrii
Voprosy Prakticheskoi Pediatrii Medicine-Pediatrics, Perinatology and Child Health
CiteScore
1.20
自引率
0.00%
发文量
50
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