Dow Eryn, Winship Ingrid
Genetic Medicine and Family Cancer Clinic, Royal Melbourne Hospital, Melbourne, Victoria, Australia.
Department of Medicine, University of Melbourne, Parkville, Victoria, Australia.
Am J Med Genet A. 2016 Dec;170(12):3323-3326. doi: 10.1002/ajmg.a.37952. Epub 2016 Sep 19.
Birt-Hogg-Dube syndrome (BHD) is an autosomal dominant disease characterised by benign cutaneous lesions, pulmonary cysts, and an increased risk of renal tumors. This rare condition is due to a mutation in the folliculin (FLCN) gene on chromosome 17q11.2, which has a role in the mechanistic/mammalian target of rapamycin (mTOR) signaling pathway of tumorigenesis. This case illustrates a patient with BHD and a renal angiomyolipoma, a neoplastic lesion not usually associated with BHD but common in Tuberous Sclerosis Complex (TSC). There is both clinical and molecular overlap between BHD and TSC, which may arise from similarities in function of the TSC and FLCN proteins in the mTOR pathway; this case further demonstrates this potential correlation. © 2016 Wiley Periodicals, Inc.
Birt-Hogg-Dube综合征(BHD)是一种常染色体显性疾病,其特征为良性皮肤病变、肺囊肿以及肾肿瘤风险增加。这种罕见病症是由17号染色体长臂11.2区的卵泡抑素(FLCN)基因突变所致,该基因在肿瘤发生的机制/哺乳动物雷帕霉素靶蛋白(mTOR)信号通路中发挥作用。本病例展示了一名患有BHD和肾血管平滑肌脂肪瘤的患者,肾血管平滑肌脂肪瘤是一种通常与BHD无关但在结节性硬化症(TSC)中常见的肿瘤性病变。BHD和TSC在临床和分子层面存在重叠,这可能源于TSC和FLCN蛋白在mTOR通路中功能的相似性;本病例进一步证明了这种潜在关联。© 2016威利期刊公司