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一名儿童多发性肿瘤性钙化症的自发消退

Spontaneous regression of multiple tumoral calcinosis in a child.

作者信息

Okada Tomoyoshi, Hara Hiroyuki, Shimojima Hiroyuki, Suzuki Hiroyuki

机构信息

Department of Dermatology, Nihon University School of Medicine, 30-1 Oyaguchi-kamimachi, Itabashi-ku, Tokyo, 173-8610, Japan.

出版信息

Eur J Dermatol. 2004 Nov-Dec;14(6):424-5.

PMID:15564210
Abstract

We report a case of multiple tumoral calcinosis on the head and back of a one-year-old boy who had no renal diseases. After an excisional biopsy of one of the tumors from the occipital region, all of the tumors spontaneously regressed without any further surgical or medical treatment. Although he had neonatal hepatitis, his liver function improved as well as the course of the spontaneous regression of the tumoral calcinosis. There has been only one case of a child with this condition in the literature.

摘要

我们报告一例一岁男童头部和背部多发性肿瘤性钙化症,该患儿无肾脏疾病。对枕部的一个肿瘤进行切除活检后,所有肿瘤未经进一步手术或药物治疗便自行消退。尽管他曾患新生儿肝炎,但其肝功能得到改善,肿瘤性钙化症的自发消退过程也得以改善。文献中仅有一例儿童患有此病。

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2
Long-term clinical outcome and phenotypic variability in hyperphosphatemic familial tumoral calcinosis and hyperphosphatemic hyperostosis syndrome caused by a novel GALNT3 mutation; case report and review of the literature.由新型GALNT3突变引起的高磷血症性家族性肿瘤性钙化症和高磷血症性骨肥厚综合征的长期临床结局及表型变异性;病例报告及文献复习
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