新生儿特发性偏侧肥大症合并肾上腺出血性假性囊肿1例分析

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摘要特发性偏侧肥大症(IH)是以一侧肢体、躯干、头面部或整个半身不对称生长、肥大为主要特征的一种先天罕见疾病,肥大可涉及软组织和(或)骨骼。该病发病率极低,患儿在儿童时期肿瘤发生风险高,需密切随访。新生儿肾上腺出血性假性囊肿是继发于新生儿肾上腺出血,其后血肿机化形成,相对少见,超声及CT动态监测可明确诊断。本文报道1例累及右侧肢体的IH合并肾上腺出血性假性囊肿者,并复习相关文献,旨在提高临床医生对该病的认识,早期确诊并密切随访可改善患儿预后。

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	刘翠莲
	王润芳
	刘晓丹
	霍琰

关键词 ：特发性偏侧肥大症(IH), 新生儿, 肢体, 肾上腺出血性假性囊肿

收稿日期: 2021-09-22

ZTFLH:

R72

通讯作者: 霍琰(hy196867@126.com)

引用本文:

刘翠莲, 王润芳, 刘晓丹, 霍琰. 新生儿特发性偏侧肥大症合并肾上腺出血性假性囊肿1例分析[J]. 中国生育健康杂志, 2022, 33(4): 376-379.

链接本文:

http://cjrh.bjmu.edu.cn/CN/ 或 http://cjrh.bjmu.edu.cn/CN/Y2022/V33/I4/376

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