Lymphomatoid Papulosis. Case in pediatric dermatological clinical practice

Q4 Medicine
D. Zaslavsky, I. A. Gorlanov, I. Belousova, E. S. Bolshakova, Anna A. Artykova, Ekaterina A. Lyamina, D. Kozlova
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引用次数: 0

Abstract

A clinical case of lymphomatoid papulosis in a 10-year-old boy is described, clinically characterized by the presence of ulcerating nodes that resolve with the atrophy formation. The patient’s differential diagnostic workup included cutaneous anaplastic large cell lymphoma, cutaneous tuberculosis, polyarteritis nodosa, erythema nodosum, deep lupus erythematosus, and alpha-1 antitrypsin deficiency. Based on the history, clinical picture, as well as laboratory and instrumental studies, the patient was diagnosed with lymphomatoid papulosis. During the examination, no concomitant neoplastic diseases were identified in the patient. All elements resolved with the outcome being hyperpigmented spots and atrophy. To date, the relapse-free period of the disease in the patient is 10 months.
淋巴瘤样丘疹病。儿科皮肤病临床实践中的病例
本病例描述了一名 10 岁男孩淋巴瘤样丘疹病的临床病例,其临床特征是出现溃疡性结节,并随着萎缩的形成而消退。患者的鉴别诊断包括皮肤无弹性大细胞淋巴瘤、皮肤结核、结节性多动脉炎、结节性红斑、深部红斑狼疮和α-1抗胰蛋白酶缺乏症。根据病史、临床表现以及实验室和仪器检查,患者被诊断为淋巴瘤样丘疹病。在检查过程中,患者没有发现并发肿瘤疾病。所有病因都得到了解决,结果是出现了色素沉着斑和萎缩。迄今为止,患者的疾病无复发期为 10 个月。
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
CiteScore
0.80
自引率
0.00%
发文量
40
审稿时长
8 weeks
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