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首页> 外文期刊>Acta Biochimica Polonica >Diagnosis and treatment difficulties in 18-year-old male patient with hereditary hemochromatosis, chronic hepatitis B, Gilbert syndrome and ulcerative colitis
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Diagnosis and treatment difficulties in 18-year-old male patient with hereditary hemochromatosis, chronic hepatitis B, Gilbert syndrome and ulcerative colitis

机译:遗传性血色素沉着,慢性乙型肝炎,吉尔伯特综合征和溃疡性结肠炎的18岁男性患者的诊断和治疗困难

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摘要

Among possible causes of chronic hepatitis in adolescents most common are infections, autoimmune disorders and metabolic diseases. Thus, diagnostic procedures should be multidirectional. This study reports diagnosis and treatment difficulties in an 18-year-old male patient with hereditary hemochromatosis (HH), ulcerative colitis (UC), chronic hepatitis B (CHB) and Gilbert syndrome. The presented case illustrates problems in diagnostics related to the presence of numerous disease conditions in one patient. It should be taken into consideration that these diseases coexisting in one patient can mutually affect their symptoms creating specific diagnostic difficulties.
机译:青少年中最常见的慢性肝炎的可能原因是感染,自身免疫性疾病和代谢性疾病。因此,诊断过程应该是多方向的。这项研究报告了患有遗传性血色素沉着病(HH),溃疡性结肠炎(UC),慢性乙型肝炎(CHB)和吉尔伯特综合征的18岁男性患者的诊断和治疗困难。提出的病例说明了与一名患者中多种疾病的存在相关的诊断问题。应当考虑到,在一名患者中并存的这些疾病会相互影响其症状,从而造成特定的诊断困难。

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