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  • Surprising genetic and pathological findings in a patient with giant bilateral periadrenal tumours: PEComas and mutations of PTCH1 in Gorlin-Goltz syndrome

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Cancer genetics
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Surprising genetic and pathological findings in a patient with giant bilateral periadrenal tumours: PEComas and mutations of PTCH1 in Gorlin-Goltz syndrome

Authors

  • Peter Igaz Department of Endocrinology, Semmelweis University Faculty of Medicine, Budapest, Hungary MTA-SE Molecular Medicine Research Group, Eötvös Loránd Research Network, Budapest, Hungary Department of Internal Medicine and Oncology, Semmelweis University Faculty of Medicine, Budapest, Hungary PubMed articlesGoogle scholar articles
  • Geza Toth Szt. Lazar Hospital, Salgotarjan, Hungary PubMed articlesGoogle scholar articles
  • Peter Nagy 1st Department of Pathology and Experimental Cancer Research, Semmelweis University Faculty of Medicine, Budapest, Hungary PubMed articlesGoogle scholar articles
  • Katalin Dezső 1st Department of Pathology and Experimental Cancer Research, Semmelweis University Faculty of Medicine, Budapest, Hungary PubMed articlesGoogle scholar articles
  • Peter Istvan Turai Department of Endocrinology, Semmelweis University Faculty of Medicine, Budapest, Hungary MTA-SE Molecular Medicine Research Group, Eötvös Loránd Research Network, Budapest, Hungary Department of Internal Medicine and Oncology, Semmelweis University Faculty of Medicine, Budapest, Hungary PubMed articlesGoogle scholar articles
  • Marta Medvecz Department of Dermatology, Venereology and Dermatooncology, Semmelweis University Faculty of Medicine, Budapest, Hungary PubMed articlesGoogle scholar articles
  • Norbert Wikonkal Department of Dermatology, Venereology and Dermatooncology, Semmelweis University Faculty of Medicine, Budapest, Hungary PubMed articlesGoogle scholar articles
  • Gergely Huszty Department of Transplantation and Surgery, Semmelweis University Faculty of Medicine, Budapest, Hungary PubMed articlesGoogle scholar articles
  • László Piros Department of Transplantation and Surgery, Semmelweis University Faculty of Medicine, Budapest, Hungary PubMed articlesGoogle scholar articles
  • Erika Toth Department of Surgical and Molecular Pathology, National Institute of Oncology, Budapest, Hungary PubMed articlesGoogle scholar articles
  • Aniko Bozsik MTA-SE Hereditary Tumors Research Group, Eötvös Loránd Research Network, Budapest, Hungary Department of Molecular Genetics, National Institute of Oncology, Budapest, Hungary PubMed articlesGoogle scholar articles
  • István Likó MTA-SE Hereditary Tumors Research Group, Eötvös Loránd Research Network, Budapest, Hungary PubMed articlesGoogle scholar articles
  • Attila Patócs MTA-SE Hereditary Tumors Research Group, Eötvös Loránd Research Network, Budapest, Hungary Department of Molecular Genetics, National Institute of Oncology, Budapest, Hungary Department of Laboratory Medicine, Semmelweis University Faculty of Medicine, Budapest, Hungary PubMed articlesGoogle scholar articles
  • Henriett Butz MTA-SE Hereditary Tumors Research Group, Eötvös Loránd Research Network, Budapest, Hungary Department of Molecular Genetics, National Institute of Oncology, Budapest, Hungary Department of Laboratory Medicine, Semmelweis University Faculty of Medicine, Budapest, Hungary PubMed articlesGoogle scholar articles
  1. Correspondence to Professor Peter Igaz, Department of Endocrinology, Semmelweis University Faculty of Medicine, Budapest, Hungary; igaz.peter{at}med.semmelweis-univ.hu
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Citation

Igaz P, Toth G, Nagy P, et al
Surprising genetic and pathological findings in a patient with giant bilateral periadrenal tumours: PEComas and mutations of PTCH1 in Gorlin-Goltz syndrome
Journal of Medical Genetics 2022;59:916-919.

Publication history

  • Received July 5, 2021
  • Accepted November 27, 2021
  • First published December 16, 2021.
Online issue publication 
November 15, 2022

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© Author(s) (or their employer(s)) 2022. No commercial re-use. See rights and permissions. Published by BMJ.