Literature DB >> 35285003

Overview of the 2022 WHO Classification of Familial Endocrine Tumor Syndromes.

Vania Nosé1, Anthony Gill2, José Manuel Cameselle Teijeiro3, Aurel Perren4, Lori Erickson5.   

Abstract

This review of the familial tumor syndromes involving the endocrine organs is focused on discussing the main updates on the upcoming fifth edition of the WHO Classification of Endocrine and Neuroendocrine Tumors. This review emphasizes updates on histopathological and molecular genetics aspects of the most important syndromes involving the endocrine organs. We describe the newly defined Familial Cancer Syndromes as MAFA-related, MEN4, and MEN5 as well as the newly reported pathological findings in DICER1 syndrome. We also describe the updates done at the new WHO on the syndromic and non-syndromic familial thyroid diseases. We emphasize the problem of diagnostic criteria, mention the new genes that are possibly involved in this group, and at the same time, touching upon the role of some immunohistochemical studies that could support the diagnosis of some of these conditions. As pathologists play an important role in identifying tumors within a familial cancer syndrome, we highlight the most important clues for raising the suspicious of a syndrome. Finally, we highlight the challenges in defining these entities as well as determining their clinical outcome in comparison with sporadic tumors. Instead of the usual subject review, we present the highlights of the updates on familial cancer syndromes by answering select questions relevant to practicing pathologists.
© 2022. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.

Entities:  

Keywords:  Endocrine familial cancer syndromes; Familial cancer syndromes; Familial tumor syndromes; Genetic tumor syndromes; Hereditary tumor syndromes

Mesh:

Substances:

Year:  2022        PMID: 35285003     DOI: 10.1007/s12022-022-09705-5

Source DB:  PubMed          Journal:  Endocr Pathol        ISSN: 1046-3976            Impact factor:   3.943


  242 in total

Review 1.  MEN4 and CDKN1B mutations: the latest of the MEN syndromes.

Authors:  Rami Alrezk; Fady Hannah-Shmouni; Constantine A Stratakis
Journal:  Endocr Relat Cancer       Date:  2017-08-19       Impact factor: 5.678

Review 2.  [Inherited tumor syndromes of gastroenteropancreatic and thoracic neuroendocrine neoplasms].

Authors:  Anne Couvelard; Jean-Yves Scoazec
Journal:  Ann Pathol       Date:  2020-02-05       Impact factor: 0.407

3.  18F-FDOPA PET/CT Imaging of MAX-Related Pheochromocytoma.

Authors:  David Taïeb; Abhishek Jha; Carole Guerin; Ying Pang; Karen T Adams; Clara C Chen; Pauline Romanet; Philippe Roche; Wassim Essamet; Alexander Ling; Martha M Quezado; Frédéric Castinetti; Fréderic Sebag; Karel Pacak
Journal:  J Clin Endocrinol Metab       Date:  2018-04-01       Impact factor: 5.958

Review 4.  MEN-4 and other multiple endocrine neoplasias due to cyclin-dependent kinase inhibitors (p27(Kip1) and p18(INK4C)) mutations.

Authors:  Marianthi Georgitsi
Journal:  Best Pract Res Clin Endocrinol Metab       Date:  2010-06       Impact factor: 4.690

5.  MAX mutations cause hereditary and sporadic pheochromocytoma and paraganglioma.

Authors:  Nelly Burnichon; Alberto Cascón; Francesca Schiavi; Nicole Paes Morales; Iñaki Comino-Méndez; Nasséra Abermil; Lucía Inglada-Pérez; Aguirre A de Cubas; Laurence Amar; Marta Barontini; Sandra Bernaldo de Quirós; Jérôme Bertherat; Yves-Jean Bignon; Marinus J Blok; Sara Bobisse; Salud Borrego; Maurizio Castellano; Philippe Chanson; María-Dolores Chiara; Eleonora P M Corssmit; Mara Giacchè; Ronald R de Krijger; Tonino Ercolino; Xavier Girerd; Encarna B Gómez-García; Alvaro Gómez-Graña; Isabelle Guilhem; Frederik J Hes; Emiliano Honrado; Esther Korpershoek; Jacques W M Lenders; Rocío Letón; Arjen R Mensenkamp; Anna Merlo; Luigi Mori; Arnaud Murat; Peggy Pierre; Pierre-François Plouin; Tamara Prodanov; Miguel Quesada-Charneco; Nan Qin; Elena Rapizzi; Victoria Raymond; Nicole Reisch; Giovanna Roncador; Macarena Ruiz-Ferrer; Frank Schillo; Alexander P A Stegmann; Carlos Suarez; Elisa Taschin; Henri J L M Timmers; Carli M J Tops; Miguel Urioste; Felix Beuschlein; Karel Pacak; Massimo Mannelli; Patricia L M Dahia; Giuseppe Opocher; Graeme Eisenhofer; Anne-Paule Gimenez-Roqueplo; Mercedes Robledo
Journal:  Clin Cancer Res       Date:  2012-03-27       Impact factor: 12.531

6.  Temozolomide treatment of a malignant pheochromocytoma and an unresectable MAX-related paraganglioma.

Authors:  Alfonso M Ferrara; Giuseppe Lombardi; Ardi Pambuku; Domenico Meringolo; Roberta Bertorelle; Margherita Nardin; Francesca Schiavi; Maurizio Iacobone; Giuseppe Opocher; Vittorina Zagonel; Stefania Zovato
Journal:  Anticancer Drugs       Date:  2018-01       Impact factor: 2.248

7.  Complex MAX Rearrangement in a Family With Malignant Pheochromocytoma, Renal Oncocytoma, and Erythrocytosis.

Authors:  Esther Korpershoek; Djamailys Koffy; Bert H Eussen; Lindsey Oudijk; Thomas G Papathomas; Francien H van Nederveen; Eric J T Belt; Gaston J H Franssen; David F J Restuccia; Niels M G Krol; Rob B van der Luijt; Richard A Feelders; Rogier A Oldenburg; Wilfred F J van Ijcken; Annelies de Klein; Wouter W de Herder; Ronald R de Krijger; Winand N M Dinjens
Journal:  J Clin Endocrinol Metab       Date:  2015-12-15       Impact factor: 5.958

8.  Clinical Characterization of the Pheochromocytoma and Paraganglioma Susceptibility Genes SDHA, TMEM127, MAX, and SDHAF2 for Gene-Informed Prevention.

Authors:  Birke Bausch; Francesca Schiavi; Ying Ni; Jenny Welander; Attila Patocs; Joanne Ngeow; Ulrich Wellner; Angelica Malinoc; Elisa Taschin; Giovanni Barbon; Virginia Lanza; Peter Söderkvist; Adam Stenman; Catharina Larsson; Fredrika Svahn; Jin-Lian Chen; Jessica Marquard; Merav Fraenkel; Martin A Walter; Mariola Peczkowska; Aleksander Prejbisz; Barbara Jarzab; Kornelia Hasse-Lazar; Stephan Petersenn; Lars C Moeller; Almuth Meyer; Nicole Reisch; Arnold Trupka; Christoph Brase; Matthias Galiano; Simon F Preuss; Pingling Kwok; Nikoletta Lendvai; Gani Berisha; Özer Makay; Carsten C Boedeker; Georges Weryha; Karoly Racz; Andrzej Januszewicz; Martin K Walz; Oliver Gimm; Giuseppe Opocher; Charis Eng; Hartmut P H Neumann
Journal:  JAMA Oncol       Date:  2017-09-01       Impact factor: 31.777

9.  Synchronous bilateral pheochromocytomas and paraganglioma with novel germline mutation in MAX: a case report.

Authors:  Masahiro Shibata; Takahiro Inaishi; Noriyuki Miyajima; Yayoi Adachi; Yuko Takano; Kenichi Nakanishi; Dai Takeuchi; Sumiyo Noda; Yuichi Aita; Kazuhiro Takekoshi; Yasuhiro Kodera; Toyone Kikumori
Journal:  Surg Case Rep       Date:  2017-12-28

10.  Somatic mutation of CDKN1B in small intestine neuroendocrine tumors.

Authors:  Joshua M Francis; Adam Kiezun; Alex H Ramos; Stefano Serra; Chandra Sekhar Pedamallu; Zhi Rong Qian; Michaela S Banck; Rahul Kanwar; Amit A Kulkarni; Anna Karpathakis; Veronica Manzo; Tanupriya Contractor; Juliet Philips; Elizabeth Nickerson; Nam Pho; Susanne M Hooshmand; Lauren K Brais; Michael S Lawrence; Trevor Pugh; Aaron McKenna; Andrey Sivachenko; Kristian Cibulskis; Scott L Carter; Akinyemi I Ojesina; Samuel Freeman; Robert T Jones; Douglas Voet; Gordon Saksena; Daniel Auclair; Robert Onofrio; Erica Shefler; Carrie Sougnez; Jonna Grimsby; Lisa Green; Niall Lennon; Tim Meyer; Martyn Caplin; Daniel C Chung; Andreas S Beutler; Shuji Ogino; Christina Thirlwell; Ramesh Shivdasani; Sylvia L Asa; Chris R Harris; Gad Getz; Matthew Kulke; Matthew Meyerson
Journal:  Nat Genet       Date:  2013-11-03       Impact factor: 38.330

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  1 in total

1.  Special Issue On the 2022 WHO Classification of Endocrine and Neuroendocrine Tumors: a New Primer for Endocrine Pathology Practice.

Authors:  Ozgur Mete
Journal:  Endocr Pathol       Date:  2022-03       Impact factor: 4.056

  1 in total

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