Non-cutaneous extranodal mature T- and natural killer (NK)-cell neoplasms: clinicopathologic features, genetics and updates

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引用次数: 0

Abstract

Non-cutaneous extranodal mature T- and natural killer (NK)-cell neoplasms represent a broad spectrum of neoplasms involving various extranodal sites, predominantly in the liver, spleen, bone marrow, gastrointestinal tract, and nasal cavity, ranging from indolent to highly aggressive diseases. Extranodal NK/T-cell lymphoma (ENKTL), aggressive NK-cell leukaemia (ANKL), and EBV-positive T-cell and NK-cell lymphoid proliferations and lymphomas of childhood, are strongly associated with Epstein-Barr virus (EBV). Overlapping clinical and histopathological features exist between entities, making differentiation challenging. A multidisciplinary approach is essential in establishing the correct diagnosis. Recent advances in genomics have provided new insights into the pathogenesis, aided in the diagnosis, prognostication, and identification of potential therapeutic targets. This article focuses on the clinicopathologic features of these entities, incorporating recent advances in genetic characterization, and highlighting features that assist in distinguishing these conditions from potential mimickers.

非皮肤结节外成熟 T 细胞和自然杀伤 (NK) 细胞肿瘤:临床病理特征、遗传学和最新进展
非皮肤结节外成熟 T 细胞和自然杀伤 (NK) 细胞肿瘤是一种涉及各种结节外部位的广泛肿瘤,主要发生在肝、脾、骨髓、胃肠道和鼻腔,从轻微到高度侵袭性疾病不等。结节外 NK/T 细胞淋巴瘤(ENKTL)、侵袭性 NK 细胞白血病(ANKL)以及 EBV 阳性的儿童 T 细胞和 NK 细胞淋巴增生和淋巴瘤与 Epstein-Barr 病毒(EBV)密切相关。不同类型的淋巴瘤在临床和组织病理学特征上存在重叠,因此很难区分。多学科方法对于确定正确诊断至关重要。基因组学的最新进展使人们对发病机制有了新的认识,有助于诊断、预后和确定潜在的治疗靶点。本文将重点介绍这些实体的临床病理特征,结合基因表征方面的最新进展,突出有助于将这些疾病与潜在的模仿者区分开来的特征。
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来源期刊
Diagnostic Histopathology
Diagnostic Histopathology Medicine-Pathology and Forensic Medicine
CiteScore
1.30
自引率
0.00%
发文量
64
期刊介绍: This monthly review journal aims to provide the practising diagnostic pathologist and trainee pathologist with up-to-date reviews on histopathology and cytology and related technical advances. Each issue contains invited articles on a variety of topics from experts in the field and includes a mini-symposium exploring one subject in greater depth. Articles consist of system-based, disease-based reviews and advances in technology. They update the readers on day-to-day diagnostic work and keep them informed of important new developments. An additional feature is the short section devoted to hypotheses; these have been refereed. There is also a correspondence section.
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