Inflammatory myofibroblastic liver tumor

A. Kaprin, S. A. Ivanov, A. Nevolskikh, L. Petrov, A. Isaeva, R. F. Zibirov, A. Izmailov
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Abstract

Inflammatory myofibroblastic tumors (inflammatory myofibroblastic tumors) IMT in the clinical practice of an oncologist are very rare diagnostic findings. Currently, the bulk of scientific publications about IMT are devoted to reviews of clinical cases. If initially IMT were considered as pseudo-tumors, now they are classified as intermediate fibroblastic/myofibroblastic tumors according to the WHO histological classification. Management of patients with hepatic IMT are debatable today. Hepatic IMT are mostly benign lesions and characterized by spontaneous regression without any treatment. However, sometimes therapeutic and surgical treatment of these lesions is necessary. Many authors recommend surgical treatment, as with conservative treatment, some patients develop relapses. This rare observation demonstrates our experience of liver resection for inflammatory myofibroblastic liver tumor in 76 year-old patient. 
炎性肌成纤维性肝肿瘤
炎性肌纤维母细胞瘤(Inflammatory myofibroblastic tumors, IMT)在肿瘤学家的临床实践中是非常罕见的诊断发现。目前,大部分关于IMT的科学出版物都致力于临床病例的综述。如果最初IMT被认为是假肿瘤,现在根据WHO的组织学分类将其分类为中间纤维母细胞/肌纤维母细胞肿瘤。目前对肝脏IMT患者的管理存在争议。肝脏IMT多为良性病变,不经治疗可自行消退。然而,有时治疗和手术治疗这些病变是必要的。许多作者建议手术治疗,与保守治疗一样,一些患者会复发。这一罕见的观察结果证实了我们对76岁患者炎性肌成纤维性肝肿瘤进行肝切除术的经验。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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