A rare case of Brooke–Spiegler syndrome

Anuja Sunkwad, S. Mahajan, J. Dave, D. Das
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Abstract

Brooke–Spiegler syndrome (BSS) is a rare autosomal dominant inherited disorder characterized by multiple skin appendageal tumors. The predominant tumors can be a cylindroma, trichoepithelioma, and/or spiradenoma. Here we report this rare entity of Brooke–Spiegler syndrome in a 50 year old female on the basis of clinico-histopathological correlation. The gene responsible for this condition is cylindromatosis gene (CYLD1) which has been mapped on chromosome 16q12–q13. However, no mutation have been detected in CYLD gene analyzed in our patient which indicates lack of genotype–phenotype correlation in this patient.
罕见的布鲁克-斯皮格勒综合症
布鲁克-斯皮格勒综合征(BSS)是一种罕见的常染色体显性遗传疾病,其特征是多发性皮肤附属物肿瘤。主要肿瘤可为柱状瘤、毛上皮瘤和/或螺旋腺瘤。在此,我们报告一例罕见的布鲁克-斯皮格勒综合征,患者为50岁女性,基于临床-组织病理学相关性。导致这种情况的基因是圆柱形病基因(CYLD1),已被定位在染色体16q12-q13上。然而,在我们的患者中,没有检测到CYLD基因突变,这表明该患者缺乏基因型-表型相关性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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