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首页> 外文期刊>Pediatric radiology >A large infiltrating fibrous hamartoma of infancy in the abdominal wall with rare associated tuberous sclerosis.
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A large infiltrating fibrous hamartoma of infancy in the abdominal wall with rare associated tuberous sclerosis.

机译:腹壁有大量婴儿浸润性纤维错构瘤,伴有罕见的结节性硬化症。

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摘要

Tuberous sclerosis is a complex autosomal-dominant neurocutaneous syndrome characterized by hamartomatous malformations of fibrous and connective tissues in various organs. Although various histologic types of soft-tissue masses can occur with tuberous sclerosis, we present a unique case of fibrous hamartoma of infancy presenting as large infiltrating cutaneous and subcutaneous masses in the abdominal wall in a 4-year-old boy with tuberous sclerosis. Although the co-occurrence of tuberous sclerosis and fibrous hamartoma of infancy is very rare, it should be considered in the differential diagnosis of subcutaneous soft-tissue masses found in children with tuberous sclerosis.
机译:结节性硬化症是一种复杂的常染色体显性遗传神经皮肤综合症,其特征是各种器官中纤维和结缔组织的错构瘤畸形。尽管结节性硬化症可发生多种组织学类型的软组织肿块,但我们介绍了一个婴儿期纤维状错构瘤的独特病例,在一个4岁的结节性硬化症男孩的腹壁中出现大的浸润性皮肤和皮下肿物。尽管结节性硬化症和婴儿纤维状错构瘤并发的情况非常少见,但在结节性硬化症儿童中发现的皮下软组织肿块的鉴别诊断中应考虑到这一点。

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