{"title":"Primary Cutaneous Diffuse Large B‑Cell Lymphoma, Leg Type: A Clinical Case","authors":"G. E. Zimnikov, A. V. Aksenenko, A. Zavialov","doi":"10.52420/umj.23.3.98","DOIUrl":null,"url":null,"abstract":"Introduction. Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type it is a rare variant of skin lymphoma that has an aggressive course and a high risk of extracutaneous manifestations.The purpose of this work is to familiarize a wide range of specialists with the clinical manifestations of a rare disease — primary cutaneous diffuse large B-cell lymphoma.Materials and methods. An interesting clinical case is presented and the medical history of a patient with B-cell lymphoma from the skin is analyzed.Results. A differential diagnosis of the disease was made. Based on the study of histological material, the final clinical diagnosis was established and further treatment tactics were determined.Discussion. The patient had spots and plaques on the lower extremities, the sole visible signs of the disease. These symptoms may suggest a positive prognosis and a gradual progression. Diagnostic measures should include gathering medical history, assessing the local condition, and carrying out an excision biopsy early in the examination process for an accurate and prompt diagnosisConclusion. Due to the rarity of this subtype of lymphoma and the limited number of domestic publications on the topic, a more detailed study and description of individual clinical cases can lead to a better understanding of the characteristics of the symptoms and the processes of pathological changes in cells, tissues, and organs. This could potentially lead to the development of more efficient methods for early diagnosis and timely treatment of the condition.","PeriodicalId":247511,"journal":{"name":"Ural Medical Journal","volume":"41 3","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-07-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Ural Medical Journal","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.52420/umj.23.3.98","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Introduction. Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type it is a rare variant of skin lymphoma that has an aggressive course and a high risk of extracutaneous manifestations.The purpose of this work is to familiarize a wide range of specialists with the clinical manifestations of a rare disease — primary cutaneous diffuse large B-cell lymphoma.Materials and methods. An interesting clinical case is presented and the medical history of a patient with B-cell lymphoma from the skin is analyzed.Results. A differential diagnosis of the disease was made. Based on the study of histological material, the final clinical diagnosis was established and further treatment tactics were determined.Discussion. The patient had spots and plaques on the lower extremities, the sole visible signs of the disease. These symptoms may suggest a positive prognosis and a gradual progression. Diagnostic measures should include gathering medical history, assessing the local condition, and carrying out an excision biopsy early in the examination process for an accurate and prompt diagnosisConclusion. Due to the rarity of this subtype of lymphoma and the limited number of domestic publications on the topic, a more detailed study and description of individual clinical cases can lead to a better understanding of the characteristics of the symptoms and the processes of pathological changes in cells, tissues, and organs. This could potentially lead to the development of more efficient methods for early diagnosis and timely treatment of the condition.
导言。原发性皮肤弥漫性大 B 细胞淋巴瘤(腿型)是一种罕见的皮肤淋巴瘤变种,病程凶险,出现皮肤外表现的风险很高。本文旨在让广大专家熟悉一种罕见疾病--原发性皮肤弥漫性大 B 细胞淋巴瘤的临床表现。本文介绍了一个有趣的临床病例,并分析了一名皮肤 B 细胞淋巴瘤患者的病史。对该病进行了鉴别诊断。讨论。患者下肢出现斑点和斑块,这是该病唯一可见的体征。这些症状可能预示着预后良好,病情会逐渐发展。诊断措施应包括收集病史、评估局部情况,并在检查过程中尽早进行切除活检,以获得准确、及时的诊断。由于该亚型淋巴瘤的罕见性和国内相关文献的有限性,对个别临床病例进行更详细的研究和描述有助于更好地了解其症状特点以及细胞、组织和器官的病理变化过程。这样就有可能开发出更有效的早期诊断和及时治疗方法。