Birt-Hogg-Dube syndrome with a renal angiomyolipoma: Further evidence of a relationship between Birt-Hogg-Dube syndrome and tuberous sclerosis complex

被引:16
|
作者
Byrne, Marguerite [1 ]
Mallipeddi, Raj [1 ]
Pichert, Gabriella [2 ]
Whittaker, Sean [1 ]
机构
[1] Guys & St Thomas Hosp, St Johns Inst Dermatol, London SE1 9RT, England
[2] Guys & St Thomas Hosp, Dept Clin Genet, London SE1 9RT, England
关键词
Birt-Hogg-Dube syndrome; tuberous sclerosis complex; angiomyolipoma; folliculin gene; CELL CARCINOMA; TUMORS; DIFFERENTIATION; ULTRASONOGRAPHY; KIDNEY; MTOR;
D O I
10.1111/j.1440-0960.2011.00738.x
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Birt-Hogg-Dube syndrome (BHDS) is an autosomal dominant condition caused by mutations in the gene which codes for folliculin (FLCN). It is characterised clinically by fibrofolliculomas, trichodiscomas, pulmonary cysts, spontaneous pneumothoraces and renal cancers. This case illustrates a patient with BHDS and a renal angiomyolipoma. Angiomyolipomas are not described as a feature of BHDS, but rather they can occur sporadically or in tuberous sclerosis complex (TSC). Recent studies suggest that clinical similarities between BHDS and TSC may be explained by FLCN and TSC proteins functioning on a common pathway, mammalian target of rapamycin. This case adds to the literature of cases with clinical similarities.
引用
收藏
页码:151 / 154
页数:4
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