Benign clear cell “sugar” tumor of the lung in a patient with Birt-Hogg-Dubé syndrome: a case report

BACKGROUND: Birt-Hogg-Dubé (BHD) syndrome is a rare inherited autosomal genodermatosis and caused by germline mutation of the folliculin (FLCN) gene, a tumor suppressor gene of which protein product is involved in mechanistic target of rapamycin (mTOR) signaling pathway regulating cell growth and me...

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Veröffentlicht in:BMC Med Genet
Hauptverfasser: Gunji-Niitsu, Yoko, Kumasaka, Toshio, Kitamura, Shigehiro, Hoshika, Yoshito, Hayashi, Takuo, Tokuda, Hitoshi, Morita, Riichiro, Kobayashi, Etsuko, Mitani, Keiko, Kikkawa, Mika, Takahashi, Kazuhisa, Seyama, Kuniaki
Format: Artigo
Sprache:Inglês
Veröffentlicht: BioMed Central 2016
Schlagworte:
Case Report
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC5117512/
https://ncbi.nlm.nih.gov/pubmed/27871249
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12881-016-0350-y
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