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首页> 外文期刊>International Journal of Biomedical and Advance Research >Castleman’s disease presenting as persistent asymptomatic cervical lymphadenopathy in a child: A very rare disease with atypical presentation
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Castleman’s disease presenting as persistent asymptomatic cervical lymphadenopathy in a child: A very rare disease with atypical presentation

机译:儿童表现为持续性无症状颈淋巴结肿大的卡斯尔曼病:一种非常罕见的非典型症状

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Castleman?? disease is a rare atypical lympho-proliferative disorder characterised by enlarged hyperplastic lymphnodes with striking vascular proliferations. A cervical location has very rarely been reported in paediatric literature. It can be unicentric or multicentric. There are mainly four histological variants, hyaline vascular type being the commonest one.?Although unicentric Castleman's disease carries a favorable prognosis in children, surgical excision is recommended to confirm the diagnosis and to rule out other causes. We report a case of unicentric cervical Castleman?? disease of neck in a 6-years old male child, who came to paediatric ward with history of right sided neck mass since 2yrs. After thorough clinical examination and investigations, complete excision of the mass was done. Histopathological examination confirmed the diagnosis of Castleman?? disease-hyaline vascular type. On follow-up for two years no recurrence has been seen.
机译:城堡人?该病是一种罕见的非典型淋巴增生性疾病,其特征在于增生性淋巴结肿大,血管增生明显。儿科文献中很少报道宫颈位置。它可以是单中心或多中心的。组织学上的变化主要有四种,其中最常见的是透明血管类型。尽管单中心性卡斯曼氏病对儿童的预后良好,但建议手术切除以确诊并排除其他原因。我们报告一例单中心宫颈Castleman病例?一个6岁男孩的颈部疾病,该男孩自2岁起就来到小儿病房,有右侧颈部肿块的病史。经过彻底的临床检查和调查,将肿块完全切除。组织病理学检查证实了Castleman的诊断?疾病-透明血管类型。随访两年未见复发。

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