儿童、青少年和年轻人皮肤淋巴瘤和淋巴样细胞增生的诊断和治疗

IF 2.2 4区 医学 Q3 HEMATOLOGY
Jamie Stokke , Annabelle Tann , Nader Kim El-Mallawany , Ilske Oschlies
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引用次数: 1

摘要

儿童、青少年和年轻人的皮肤淋巴瘤和淋巴增生(LPD)是一组异质性淋巴肿瘤,对临床医生和病理学家来说都是一个巨大的诊断挑战。尽管总体而言很罕见,但皮肤淋巴瘤/LPD发生在现实世界中,对鉴别诊断、潜在并发症和各种治疗方法的认识将有助于确保最佳的诊断检查和临床管理。涉及皮肤的淋巴瘤/LPD可以作为原发性皮肤病发生在特征性淋巴瘤/LPD局限于皮肤的患者中,也可以作为继发性全身性疾病发生在患者中。这篇综述将全面总结发生在CAYA人群中的原发性皮肤淋巴瘤/LPD,以及那些有继发性皮肤受累倾向的CAYA系统性淋巴瘤/LPD。关注CAYA中最常见的原发性实体包括淋巴瘤样丘疹病、原发性皮肤间变性大细胞淋巴瘤、蕈样肉芽肿、皮下脂膜炎样T细胞淋巴瘤和疫苗样水疱性淋巴增生性疾病。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Diagnosis and management of cutaneous lymphomas and lymphoid proliferations in children, adolescents and young adults (CAYA)

Cutaneous lymphomas and lymphoid proliferations (LPD) in children, adolescents, and young adults (CAYA) are a heterogeneous group of lymphoid neoplasms that present formidable diagnostic challenges to clinicians and pathologists alike. Although rare overall, cutaneous lymphomas/LPD occur in real-world settings and awareness of the differential diagnosis, potential complications, and various therapeutic approaches will help ensure the optimal diagnostic work-up and clinical management. Lymphomas/LPD involving the skin can occur as primary cutaneous disease in a patient that characteristically has lymphoma/LPD confined to the skin, or as secondary involvement in patients with systemic disease. This review will comprehensively summarize both primary cutaneous lymphomas/LPD that occur in the CAYA population as well as those CAYA systemic lymphomas/LPD with propensity for secondary cutaneous involvement. Focus on the most common primary entities occurring in CAYA will include lymphomatoid papulosis, primary cutaneous anaplastic large cell lymphoma, mycosis fungoides, subcutaneous panniculitis-like T-cell lymphoma, and hydroa vacciniforme lymphoproliferative disorder.

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来源期刊
CiteScore
4.20
自引率
0.00%
发文量
42
审稿时长
35 days
期刊介绍: Best Practice & Research Clinical Haematology publishes review articles integrating the results from the latest original research articles into practical, evidence-based review articles. These articles seek to address the key clinical issues of diagnosis, treatment and patient management. Each issue follows a problem-orientated approach which focuses on the key questions to be addressed, clearly defining what is known and not known, covering the spectrum of clinical and laboratory haematological practice and research. Although most reviews are invited, the Editor welcomes suggestions from potential authors.
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