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跟骨前先天性纤维脂肪性错构瘤:4例报告

Precalcaneal congenital fibrolipomatous hamartoma: a report of four cases.

作者信息

Ortega-Monzó C, Molina-Gallardo I, Monteagudo-Castro C, Cardá-Batalla C, Pinazo-Canales I, Smith-Ferres V, Calduch-Rodríguez L, Jordá-Cuevas E

机构信息

Departments of Dermatology, Pathology, and Molecular Biology, University Clinic Hospital of Valencia, Valencia, Spain.

出版信息

Pediatr Dermatol. 2000 Nov-Dec;17(6):429-31. doi: 10.1046/j.1525-1470.2000.01816.x.

Abstract

Four infants had soft, skin-colored nodules in the midline plantar region of the heels since birth. The lesions were asymptomatic, bilateral, and symmetric, and measured approximately 1 cm in diameter. Their size increased in proportion to the growth of the child. In three infants the lesions persisted at 1 year of age, while in the fourth they remained at age 12 years. The nodules were not associated with any other disease or abnormality. A review of the literature revealed only one Argentinean series comprising four cases, and two communications at international pediatric congresses by French and American authors who reported five and three cases, respectively. We describe four additional cases of precalcaneal congenital fibrolipomatous hamartoma and comment on their histopathologic and ultrastructural characteristics.

摘要

四名婴儿自出生起在足跟足底中线区域有柔软的肤色结节。这些损害无症状,双侧对称,直径约1厘米。其大小随儿童生长而相应增大。三名婴儿的损害在1岁时持续存在,而第四名婴儿的损害在12岁时仍存在。这些结节与任何其他疾病或异常均无关联。文献回顾显示,仅有一篇阿根廷的系列报道包含4例病例,以及法国和美国作者在国际儿科学术会议上分别报告5例和3例病例的两篇通讯。我们描述另外4例跟骨前先天性纤维脂肪性错构瘤病例,并对其组织病理学和超微结构特征进行评论。

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