Peripheral lymphadenopathy of unknown origin in adults: a diagnostic approach emphasizing the malignancy hypothesis.

IF 2.1 4区 医学 Q2 MEDICINE, GENERAL & INTERNAL
Ivana Hanzalova, Maurice Matter
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引用次数: 0

Abstract

The term lymphadenopathy refers to an abnormality in size, consistency or morphological aspect of one or several lymph nodes. Although lymphadenopathies are commonly observed in everyday clinical practice, the difficulty of differentiating benign and malignant disease may delay therapeutic approaches. The present review aims to update diagnostic algorithms in different clinical situations based on the currently available literature. A literature review was performed to assess current knowledge of and to update the diagnostic approach. A short clinical vignette was used as an example of a typical clinical presentation. This case of metastatic lymphadenopathy with incomplete patient history demonstrates how misleading such lymphadenopathy may be, leading to a delayed diagnosis and even a fatal outcome. Any lymphadenopathy persisting for more than 2 weeks should be considered suspicious and deserves further investigation. Precise clinical examination, meticulous history-taking and a search for associated symptomatology are still cornerstones for diagnosing the origin of the condition. The next diagnostic step depends on the anatomical region and the specific patient's situation. Imaging starts with ultrasound, while computed tomography (CT) and magnetic resonance imaging (MRI) allow assessment of the surrounding structures. If the diagnosis remains uncertain, tissue sampling and histological analyses should be performed. Except for head and neck loco-regional lymphadenopathy, there are no methodical guidelines for persistent lymphadenopathy. The present review clarifies several confusing and complex situations. The accuracy of fine needle aspiration cytology could be increased by using core needle biopsy with immunocytologic and flow cytometric methods. Notably, except in the head and neck area, open biopsy remains the best option when lymphoma is suspected or when inconclusive results of previous fine needle aspiration cytology or core needle biopsy are obtained. The incidence of malignant lymphadenopathy varies with its location and the various diagnostic strategies. In metastatic lymphadenopathy of unknown primary origin, European Society for Medical Oncology (ESMO) guidelines and modern methods like next-generation sequencing (NGS) may help to manage such complex cases.

原因不明的成人外周淋巴结病:强调恶性假说的诊断方法。
淋巴腺病是指一个或多个淋巴结在大小、稠度或形态方面的异常。虽然淋巴腺病在日常临床实践中很常见,但由于难以区分良性和恶性疾病,可能会延误治疗方法。本综述旨在根据现有文献更新不同临床情况下的诊断算法。我们进行了文献综述,以评估当前对诊断方法的了解并更新诊断方法。我们以一个简短的临床案例作为典型的临床表现。这例转移性淋巴结病病史不完整的病例表明,这种淋巴结病可能会误导患者,导致延误诊断,甚至造成致命后果。任何持续超过两周的淋巴结病都应被视为可疑,值得进一步检查。精确的临床检查、细致的病史采集和寻找相关症状仍然是诊断病因的基石。下一步诊断取决于解剖区域和患者的具体情况。首先进行超声波检查,然后通过计算机断层扫描(CT)和磁共振成像(MRI)对周围结构进行评估。如果诊断仍不确定,则应进行组织取样和组织学分析。除头颈部局部区域淋巴结病外,目前还没有针对持续性淋巴结病的方法指南。本综述澄清了一些令人困惑的复杂情况。通过使用核心针活检和免疫细胞学及流式细胞术方法,可以提高细针穿刺细胞学检查的准确性。值得注意的是,除头颈部外,当怀疑淋巴瘤或之前的细针穿刺细胞学检查或核心针活检结果不确定时,开放活检仍是最佳选择。恶性淋巴结病的发病率因淋巴结病的部位和各种诊断策略而异。对于原发来源不明的转移性淋巴结病,欧洲肿瘤内科学会(ESMO)指南和下一代测序(NGS)等现代方法可能有助于处理这类复杂病例。
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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来源期刊
Swiss medical weekly
Swiss medical weekly 医学-医学:内科
CiteScore
5.00
自引率
0.00%
发文量
0
审稿时长
3-8 weeks
期刊介绍: The Swiss Medical Weekly accepts for consideration original and review articles from all fields of medicine. The quality of SMW publications is guaranteed by a consistent policy of rigorous single-blind peer review. All editorial decisions are made by research-active academics.
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