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酷似急性阑尾炎的肠系膜淋巴结菊池-藤本病。

Kikuchi- Fujimoto disease of mesenteric lymph nodes mimicking acute appendicitis.

作者信息

Shrestha Anne, Newton Katie, Benbow Emyr, Kushwaha Rajeev

机构信息

Department of Surgery, Manchester Royal Infirmary, Oxford Road, Manchester, M13 9WL.

出版信息

JNMA J Nepal Med Assoc. 2013 Oct-Dec;52(192):627-30.

Abstract

Kikuchi-Fujimoto disease, or histiocytic necrotising lymphadenopathy of unknown aetiology, is a rare, benign and self-limiting cause of lymphadenopathy often involving the cervical nodes, and rarely presenting with mesenteric lymphadenopathy. We present a 26-year-old Caucasian male, who presented with right iliac fossa pain and low grade pyrexia, mimicking acute appendicitis. He underwent a laparatomy and an extended right hemi-colectomy for a caecal mass. Histology of the specimen showed lymph nodes with extensive areas of necrosis, with abnormal architecture suggesting Kikuchi-Fujimoto lymphadenopathy. This was further confirmed by immunohistochemistry. In this context maintenance of a high index of suspicion of this condition can avoid major surgical interventions. We describe the management of our case of Kikuchi-Fujimoto's disease involving the mesenteric nodes and provide an up to date review of the pertinent literature on this subject.

摘要

菊池-藤本病,即病因不明的组织细胞坏死性淋巴结病,是一种罕见的、良性的、自限性的淋巴结病病因,常累及颈部淋巴结,很少表现为肠系膜淋巴结病。我们报告一名26岁的白种男性,他表现为右下腹疼痛和低热,酷似急性阑尾炎。他因盲肠肿物接受了剖腹手术和扩大右半结肠切除术。标本组织学检查显示淋巴结有广泛坏死区域,结构异常提示菊池-藤本病淋巴结病。免疫组化进一步证实了这一点。在这种情况下,对该病保持高度怀疑指数可避免重大手术干预。我们描述了我们这例累及肠系膜淋巴结的菊池-藤本病的治疗,并对该主题的相关文献进行了最新综述。

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