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[罕见淋巴瘤致急腹症——病例研究]

[Rare lymphoma causing acute abdomen - Case study].

作者信息

Czeller Dániel, Solymosi Attila, Máté Miklós

机构信息

Sebészeti Profil, Szent Imre Egyetemi Oktatókórház 1115 Budapest Tétényi út 12-16.

出版信息

Magy Seb. 2019 Sep;72(3):112-114. doi: 10.1556/1046.72.2019.3.5.

Abstract

Lymphomas are rare entities in the gastrointestinal tract. The so-called Burkitt-like lymphoma belongs to the non-Hodgkin lymphoma group, and it is quite an aggressive, rapid-growing, but potentially curable disease. Surgeons mostly encounter with this tumor as a solid mass which causes abdominal pain, or as a cause of bowel obstruction or perforation. Our aim was to present a case, when Burkitt-like lymphoma caused acute abdominal symptoms without alarming complaints, obstruction or perforation. Furthermore we review and summarize the relevant literature data on this topic. Regarding our case we can claim that histological investigation and multidisciplinary approach are essential to make the diagnosis and to start the treatment as early as possible.

摘要

淋巴瘤在胃肠道中较为罕见。所谓的伯基特样淋巴瘤属于非霍奇金淋巴瘤组,是一种侵袭性强、生长迅速但有可能治愈的疾病。外科医生大多遇到这种肿瘤时,它表现为引起腹痛的实性肿块,或是肠梗阻或肠穿孔的病因。我们的目的是呈现这样一个病例,即伯基特样淋巴瘤引发急性腹部症状,但无警示性主诉、梗阻或穿孔。此外,我们回顾并总结了关于该主题的相关文献数据。就我们的病例而言,我们可以宣称组织学检查和多学科方法对于做出诊断并尽早开始治疗至关重要。

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