Are lung cysts in renal cell cancer (RCC) patients an indication for FLCN mutation analysis?

被引:4
作者
Johannesma, Paul C. [1 ]
Houweling, Arjan C. [2 ]
Menko, Fred H. [3 ]
van de Beek, I. [2 ]
Reinhard, Rinze [4 ]
Gille, Johan J. P. [2 ]
van Waesberghe, JanHein T. M. [4 ]
Thunnissen, Erik [5 ]
Starink, Theo M. [6 ]
Postmus, Pieter E. [7 ]
van Moorselaar, R. Jeroen A. [8 ]
机构
[1] Vrije Univ Amsterdam Med Ctr, Dept Pulm Dis, POB 7057, NL-1007 MB Amsterdam, Netherlands
[2] Vrije Univ Amsterdam Med Ctr, Dept Clin Genet, NL-1007 MB Amsterdam, Netherlands
[3] Netherlands Canc Inst, Family Canc Clin, Amsterdam, Netherlands
[4] Vrije Univ Amsterdam Med Ctr, Dept Radiol, NL-1007 MB Amsterdam, Netherlands
[5] Vrije Univ Amsterdam Med Ctr, Dept Pathol, NL-1007 MB Amsterdam, Netherlands
[6] Leiden Univ, Dept Dermatol, Med Ctr, Leiden, Netherlands
[7] Univ Liverpool, Liverpool Heart & Chest Hosp, Clatterbridge Canc Ctr, Dept Mol & Clin Canc Med, Liverpool L69 3BX, Merseyside, England
[8] Vrije Univ Amsterdam Med Ctr, Dept Urol, NL-1007 MB Amsterdam, Netherlands
关键词
Birt-Hogg-Dube syndrome; BHD; Folliculin; Pneumothorax; Renal cell cancer; RCC; HOGG-DUBE SYNDROME;
D O I
10.1007/s10689-015-9853-5
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Renal cell cancer (RCC) represents 2-3 % of all cancers and is the most lethal of the urologic malignancies, in a minority of cases caused by a genetic predisposition. Birt-Hogg-Dube syndrome (BHD) is one of the hereditary renal cancer syndromes. As the histological subtype and clinical presentation in BHD are highly variable, this syndrome is easily missed. Lung cysts-mainly under the main carina-are reported to be present in over 90 % of all BHD patients and might be an important clue in differentiating between sporadic RCC and BHD associated RCC. We conducted a retrospective study among patients diagnosed with sporadic RCC, wherein we retrospectively scored for the presence of lung cysts on thoracic CT. We performed FLCN mutation analysis in 8 RCC patients with at least one lung cysts under the carina. No mutations were identified. We compared the radiological findings in the FLCN negative patients to those in 4 known BHD patients and found multiple basal lung cysts were present significantly more frequent in FLCN mutation carriers and may be an indication for BHD syndrome in apparent sporadic RCC patients.
引用
收藏
页码:297 / 300
页数:4
相关论文
共 10 条
[1]  
[Anonymous], 2018, ANTI-CANCER DRUG, DOI [DOI 10.3322/caac.20115, DOI 10.1097/CAD.0000000000000617]
[2]   Folliculin encoded by the BHD gene interacts with a binding protein, FNIP1, and AMPK, and is involved in AMPK and mTOR signaling [J].
Baba, Masaya ;
Hong, Seung-Beom ;
Sharma, Nirmala ;
Warren, Michelle B. ;
Nickerson, Michael L. ;
Iwamatsu, Akihiro ;
Esposito, Dominic ;
Gillette, William K. ;
Hopkins, Ralph F., III ;
Hartley, James L. ;
Furihata, Mutsuo ;
Oishi, Shinya ;
Zhen, Wei ;
Burke, Terrence R., Jr. ;
Linehan, W. Marston ;
Schmidt, Laura S. ;
Zbar, Berton .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (42) :15552-15557
[3]   Distinguishing the histological and radiological features of cystic lung disease in Birt-Hogg-Dube syndrome from those of tobacco-related spontaneous pneumothorax [J].
Fabre, Aurelie ;
Borie, Raphael ;
Debray, Marie Pierre ;
Crestani, Bruno ;
Danel, Claire .
HISTOPATHOLOGY, 2014, 64 (05) :741-749
[4]   Estimates of worldwide burden of cancer in 2008: GLOBOCAN 2008 [J].
Ferlay, Jacques ;
Shin, Hai-Rim ;
Bray, Freddie ;
Forman, David ;
Mathers, Colin ;
Parkin, Donald Maxwell .
INTERNATIONAL JOURNAL OF CANCER, 2010, 127 (12) :2893-2917
[5]   Renal cancer and pneumothorax risk in Birt-Hogg-Dube syndrome; an analysis of 115 FLCN mutation carriers from 35 BHD families [J].
Houweling, A. C. ;
Gijezen, L. M. ;
Jonker, M. A. ;
van Doorn, M. B. A. ;
Oldenburg, R. A. ;
van Spaendonck-Zwarts, K. Y. ;
Leter, E. M. ;
van Os, T. A. ;
van Grieken, N. C. T. ;
Jaspars, E. H. ;
de Jong, M. M. ;
Bongers, E. M. H. F. ;
Johannesma, P. C. ;
Postmus, P. E. ;
van Moorselaar, R. J. A. ;
van Waesberghe, J-H T. M. ;
Starink, T. M. ;
van Steensel, M. A. M. ;
Gille, J. J. P. ;
Menko, F. H. .
BRITISH JOURNAL OF CANCER, 2011, 105 (12) :1912-1919
[6]   Mode of presentation of renal cell carcinoma provides prognostic information [J].
Lee, CT ;
Katz, J ;
Fearn, PA ;
Russo, P .
UROLOGIC ONCOLOGY, 2002, 7 (04) :135-140
[7]  
Maffe A, 2014, ATLAS GENET CYTOGENE, V18, P521
[8]   Birt-Hogg-Dube syndrome: diagnosis and management [J].
Menko, Fred H. ;
van Steensel, Maurice A. M. ;
Giraud, Sophie ;
Friis-Hansen, Lennart ;
Richard, Stephane ;
Ungari, Silvana ;
Nordenskjold, Magnus ;
Hansen, Thomas v. O. ;
Solly, John ;
Maher, Eamonn R. .
LANCET ONCOLOGY, 2009, 10 (12) :1199-1206
[9]   Germline BHD-mutation spectrum and phenotype analysis of a large cohort of families with Birt-Hogg-Dube syndrome [J].
Schmidt, LS ;
Nickerson, ML ;
Warren, MB ;
Glenn, GM ;
Toro, JR ;
Merino, MJ ;
Turner, ML ;
Choyke, PL ;
Sharma, N ;
Peterson, J ;
Morrison, P ;
Maher, ER ;
Walther, MM ;
Zbar, B ;
Linehan, WM .
AMERICAN JOURNAL OF HUMAN GENETICS, 2005, 76 (06) :1023-1033
[10]   Hereditary Renal Cancer Syndromes: An Update of a Systematic Review [J].
Verine, Jerome ;
Pluvinage, Amelie ;
Bousquet, Guilhem ;
Lehmann-Che, Jacqueline ;
de Bazelaire, Cedric ;
Soufir, Nadem ;
Mongiat-Artus, Pierre .
EUROPEAN UROLOGY, 2010, 58 (05) :701-710