Literature DB >> 31383958

Carbonic anhydrase 9 immunohistochemistry as a tool to predict or validate germline and somatic VHL mutations in pheochromocytoma and paraganglioma-a retrospective and prospective study.

Judith Favier1, Tchao Meatchi2,3, Estelle Robidel2, Cécile Badoual2,3, Mathilde Sibony4,5, An Thach Nguyen3, Anne-Paule Gimenez-Roqueplo2,6,7, Nelly Burnichon2,6.   

Abstract

The development of pheochromocytomas and paragangliomas is strongly linked to the presence of germline mutations in more than 15 predisposing genes. Among them, germline and somatic VHL mutations account for ~10% of all cases. In contrast with SDHA and SDHB immunohistochemistries that are routinely used to validate SDHx gene mutations, there is no such tool available for VHL mutations. The aim of this study was to evaluate whether CA9 immunostaining could be used as a tool to predict the presence or validate the pathogenicity of VHL gene mutations in paraganglioma. Immunohistochemistry for CA9 was performed on 207 tumors. A retrospective series of 100 paragangliomas with known mutation status for paraganglioma susceptibility genes was first investigated. Then, a prospective series of 107 paragangliomas was investigated for CA9 immunostaining followed by germline and/or somatic genetic testing of all paraganglioma susceptibility genes by next-generation sequencing. Cytosolic CA9 protein expression was heterogeneous in the different samples. However, we observed that a membranous CA9 staining was almost exclusively observed in VHL-related cases. Forty two of 48 (88%) VHL-mutated samples showed a CA9 membranous immunostaining. Positive cells were either isolated, varying from 1 or 2 cells (5% of cases) to 10-20 cells per tumor block (35% of cases), grouped in areas of focal positivity representing between 1 and 20% of the tissue section (35% of cases), or widely distributed on 80-100% of the tumor sections (25% of samples). In contrast, 142/159 (91%) of non-VHL-mutated tumors presented no membrane CA9 localization. Our results demonstrate that VHL gene mutations can be predicted or validated reliably by an easy-to-perform and low-cost immunohistochemical procedure. CA9 immunohistochemistry on paragangliomas will improve the diagnosis of VHL-related disease, which is important for the surveillance and therapeutic management of paraganglioma patients, and in case of germline mutation, their family members.

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Year:  2019        PMID: 31383958     DOI: 10.1038/s41379-019-0343-4

Source DB:  PubMed          Journal:  Mod Pathol        ISSN: 0893-3952            Impact factor:   7.842


  8 in total

Review 1.  Overview of the 2022 WHO Classification of Paragangliomas and Pheochromocytomas.

Authors:  Ozgur Mete; Sylvia L Asa; Anthony J Gill; Noriko Kimura; Ronald R de Krijger; Arthur Tischler
Journal:  Endocr Pathol       Date:  2022-03-13       Impact factor: 3.943

Review 2.  Update from the 5th Edition of the World Health Organization Classification of Head and Neck Tumors: Familial Tumor Syndromes.

Authors:  Vania Nosé; Alexander J Lazar
Journal:  Head Neck Pathol       Date:  2022-03-21

Review 3.  Update from the 5th Edition of the World Health Organization Classification of Head and Neck Tumors: Overview of the 2022 WHO Classification of Head and Neck Neuroendocrine Neoplasms.

Authors:  Ozgur Mete; Bruce M Wenig
Journal:  Head Neck Pathol       Date:  2022-03-21

4.  Genetic stratification of inherited and sporadic phaeochromocytoma and paraganglioma: implications for precision medicine.

Authors:  Ruth Casey; Hartmut P H Neumann; Eamonn R Maher
Journal:  Hum Mol Genet       Date:  2020-10-20       Impact factor: 6.150

Review 5.  Pheochromocytoma/paraganglioma: recent updates in genetics, biochemistry, immunohistochemistry, metabolomics, imaging and therapeutic options.

Authors:  Karren Antonio; Ma Margarita Noreen Valdez; Leilani Mercado-Asis; David Taïeb; Karel Pacak
Journal:  Gland Surg       Date:  2020-02

Review 6.  Challenges in Paragangliomas and Pheochromocytomas: from Histology to Molecular Immunohistochemistry.

Authors:  C Christofer Juhlin
Journal:  Endocr Pathol       Date:  2021-03-25       Impact factor: 3.943

7.  Germline mutations in the new E1' cryptic exon of the VHL gene in patients with tumours of von Hippel-Lindau disease spectrum or with paraganglioma.

Authors:  Bruna Calsina; Shahida Flores; Sophie Giraud; Marion Lenglet; Alexandre Buffet; Pauline Romanet; Elisa Deflorenne; Javier Aller; Isabelle Bourdeau; Brigitte Bressac-de Paillerets; María Calatayud; Caroline Dehais; Erwan De Mones Del Pujol; Atanaska Elenkova; Philippe Herman; Peter Kamenický; Sophie Lejeune; Jean Louis Sadoul; Anne Barlier; Stephane Richard; Judith Favier; Nelly Burnichon; Betty Gardie; Patricia L Dahia; Mercedes Robledo; Anne-Paule Gimenez-Roqueplo
Journal:  J Med Genet       Date:  2020-01-29       Impact factor: 6.318

Review 8.  Preoperative Diagnosis of Abdominal Extra-Adrenal Paragangliomas with Fine-Needle Biopsy.

Authors:  Ilias P Nikas; Angela Ishak; Mousa M AlRawashdeh; Eirini Klapsinou; Athanasia Sepsa; George N Tzimas; Dimitrios Panagiotakopoulos; Dimitrios Papaioannou; Charitini Salla
Journal:  Diagnostics (Basel)       Date:  2022-07-28
  8 in total

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