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菊池-藤本病作为良性淋巴结病的罕见病因及(18)F-FDG PET/CT表现

Kikuchi-Fujimoto disease as a rare cause of benign lymphadenopathy and (18)F-FDG PET/CT findings.

作者信息

Erhamamci Seval, Reyhan Mehmet, Kocer Nazim Emrah

机构信息

Department of Nuclear Medicine, Baskent University, Faculty of Medicine, Saray Street No. 1, 42080: Selcuklu, Konya, Turkey.

出版信息

Hell J Nucl Med. 2014 Jan-Apr;17(1):41-4. doi: 10.1967/s002449910115. Epub 2014 Feb 25.

Abstract

Kikuchi-Fujimoto disease (KFD) is an uncommon benign and self-limited disease, characterized by cervical lymphadenopathy. This disease is generally diagnosed on the basis of an excisional biopsy of affected lymph nodes. However, clinical presentation and histopathological findings of KFD could lead to a wrong initial diagnosis, of tuberculosis, systemic lupus erythymatosus or malignant lymphoma. Laboratory tests are not specific. Imaging modalitites give confusing results. Affected lymph nodes of patients with KFD can exibit (18)F-FDG uptake on PET/CT imaging similar to malignant lymphoma. Therefore, the differential diagnosis of KFD should be considered in patients with cervical and/or generalized lymphadenopathy. Accurate diagnosis of KFD by histology is essential in avoiding unnecessary emotional and mental distress associated with the diagnosis of lymphoma.

摘要

菊池-藤本病(KFD)是一种罕见的良性自限性疾病,以颈部淋巴结病为特征。该病通常根据受累淋巴结的切除活检进行诊断。然而,KFD的临床表现和组织病理学发现可能导致最初误诊为结核病、系统性红斑狼疮或恶性淋巴瘤。实验室检查不具有特异性。影像学检查结果令人困惑。KFD患者受累淋巴结在PET/CT成像上可表现出与恶性淋巴瘤相似的(18)F-FDG摄取。因此,对于有颈部和/或全身淋巴结病的患者,应考虑KFD的鉴别诊断。通过组织学准确诊断KFD对于避免与淋巴瘤诊断相关的不必要的情绪和精神困扰至关重要。

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