罗莎-多尔夫曼病在儿童时期呈现无全身症状
Lakshmi S Arvapalli1, Venkat Tej Sai Bodla2, Hari P Bodla3
1Department of General Medicine, Rajiv Gandhi Institute of Medical Sciences, Ongole, India.
BMJ case reports
|November 5, 2025
概括
罗莎-多夫曼病 (RDD) 是一种罕见的囊细胞瘤,在儿童中可以无症状出现. 这一案例突出了RDD.
科学领域:
- 儿科血液学 儿科血液学
- 组织细胞化 (histiocytosis) 是一种
- 罕见疾病 罕见疾病
背景情况:
- 罗莎-多尔夫曼病 (RDD) 是一种罕见的非朗格汉斯细胞囊炎.
- 它通常表现为大规模的淋巴腺病变.
- 儿科病例的诊断可能是具有挑战性的,因为呈现的不同.
研究的目的:
- 报告儿童患有无症状罗赛-多夫曼病的病例.
- 强调在儿科RDD中良性和自我限制的课程的潜力.
- 讨论儿童早期RDD的诊断和管理方面的考虑.
主要方法:
- 一个患有广泛淋巴腺病的儿科患者的病例报告.
- 通过细针吸收细胞学来确认诊断.
- 临床随访,以评估疾病进展和治疗有效性.
主要成果:
- 一名儿童出现了无痛的宫,腹部和部淋巴腺症.
- 尽管发生了广泛的节点参与,但患者仍然无症状.
- 罗赛-多夫曼病的诊断通过精细针吸收细胞学得到证实.
结论:
- 罗赛-多夫曼病在儿科患者中可以无症状呈现.
- 对于无症状的RDD,保守的治疗可能是有效的.
- 在一些儿童中,这种疾病可能表现为良性,自我限制的过程,需要仔细观察.
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