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Published in: Endocrine Pathology 1/2022

01-03-2022

Overview of the 2022 WHO Classification of Familial Endocrine Tumor Syndromes

Authors: Vania Nosé, Anthony Gill, José Manuel Cameselle Teijeiro, Aurel Perren, Lori Erickson

Published in: Endocrine Pathology | Issue 1/2022

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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.
Literature
17.
go back to reference Yagita M, Itoh K, Tsudo M et al (1989) Involvement of both Tac and non-Tac interleukin 2-binding peptides in the interleukin 2-dependent proliferation of human tumor-infiltrating lymphocytes. Cancer Res 49:1154-9PubMed Yagita M, Itoh K, Tsudo M et al (1989) Involvement of both Tac and non-Tac interleukin 2-binding peptides in the interleukin 2-dependent proliferation of human tumor-infiltrating lymphocytes. Cancer Res 49:1154-9PubMed
20.
47.
go back to reference Oshima J, Martin GM and Hisama FM (1993) Werner Syndrome. GeneReviews((R)) Oshima J, Martin GM and Hisama FM (1993) Werner Syndrome. GeneReviews((R))
48.
go back to reference Yehia L and Eng C (1993) PTEN Hamartoma Tumor Syndrome. GeneReviews((R)) Yehia L and Eng C (1993) PTEN Hamartoma Tumor Syndrome. GeneReviews((R))
88.
94.
go back to reference Jackson CE, Norum RA, Boyd SB et al (1990) Hereditary hyperparathyroidism and multiple ossifying jaw fibromas: a clinically and genetically distinct syndrome. Surgery 108:1006–12; discussion 1012–3 Jackson CE, Norum RA, Boyd SB et al (1990) Hereditary hyperparathyroidism and multiple ossifying jaw fibromas: a clinically and genetically distinct syndrome. Surgery 108:1006–12; discussion 1012–3
119.
go back to reference Singh Ospina N, Sebo TJ, Thompson GB, Clarke BL and Young WF, Jr. (2016) Prevalence of parathyroid carcinoma in 348 patients with multiple endocrine neoplasia type 1 - case report and review of the literature. Clin Endocrinol (Oxf) 84:244-249 https://doi.org/10.1111/cen.12714CrossRef Singh Ospina N, Sebo TJ, Thompson GB, Clarke BL and Young WF, Jr. (2016) Prevalence of parathyroid carcinoma in 348 patients with multiple endocrine neoplasia type 1 - case report and review of the literature. Clin Endocrinol (Oxf) 84:244-249 https://​doi.​org/​10.​1111/​cen.​12714CrossRef
125.
go back to reference Szabo J, Heath B, Hill VM et al (1995) Hereditary hyperparathyroidism-jaw tumor syndrome: the endocrine tumor gene HRPT2 maps to chromosome 1q21-q31. Am J Hum Genet 56:944-50PubMedPubMedCentral Szabo J, Heath B, Hill VM et al (1995) Hereditary hyperparathyroidism-jaw tumor syndrome: the endocrine tumor gene HRPT2 maps to chromosome 1q21-q31. Am J Hum Genet 56:944-50PubMedPubMedCentral
135.
go back to reference Yamasaki M, Sato Y, Nomura T, Sato F, Uchino S and Mimata H (2017) Composite paraganglioma-ganglioneuroma concomitant with adrenal metastasis of medullary thyroid carcinoma in a patient with multiple endocrine neoplasia type 2B: A case report. Asian J Endosc Surg 10:66-69 https://doi.org/10.1111/ases.12332CrossRefPubMed Yamasaki M, Sato Y, Nomura T, Sato F, Uchino S and Mimata H (2017) Composite paraganglioma-ganglioneuroma concomitant with adrenal metastasis of medullary thyroid carcinoma in a patient with multiple endocrine neoplasia type 2B: A case report. Asian J Endosc Surg 10:66-69 https://​doi.​org/​10.​1111/​ases.​12332CrossRefPubMed
145.
go back to reference Hunt JL, Carty SE, Yim JH, Murphy J and Barnes L (2005) Allelic loss in parathyroid neoplasia can help characterize malignancy. Am J Surg Pathol 29:1049-55CrossRefPubMed Hunt JL, Carty SE, Yim JH, Murphy J and Barnes L (2005) Allelic loss in parathyroid neoplasia can help characterize malignancy. Am J Surg Pathol 29:1049-55CrossRefPubMed
170.
go back to reference Binderup ML, Bisgaard ML, Harbud V et al (2013) Von Hippel-Lindau disease (vHL). National clinical guideline for diagnosis and surveillance in Denmark. 3rd edition. Dan Med J 60:B4763 Binderup ML, Bisgaard ML, Harbud V et al (2013) Von Hippel-Lindau disease (vHL). National clinical guideline for diagnosis and surveillance in Denmark. 3rd edition. Dan Med J 60:B4763
175.
go back to reference Sakorafas GH, Giannopoulos GA, Parasi A et al (2008) Large somatostatin-producing endocrine carcinoma of the ampulla of vater in association with GIST in a patient with von Recklinghausen's disease. Case report and review of the literature. JOP 9:633-9PubMed Sakorafas GH, Giannopoulos GA, Parasi A et al (2008) Large somatostatin-producing endocrine carcinoma of the ampulla of vater in association with GIST in a patient with von Recklinghausen's disease. Case report and review of the literature. JOP 9:633-9PubMed
177.
go back to reference Deschamps L, Dokmak S, Guedj N, Ruszniewski P, Sauvanet A and Couvelard A (2010) Mixed endocrine somatostatinoma of the ampulla of vater associated with a neurofibromatosis type 1: a case report and review of the literature. JOP 11:64-8PubMed Deschamps L, Dokmak S, Guedj N, Ruszniewski P, Sauvanet A and Couvelard A (2010) Mixed endocrine somatostatinoma of the ampulla of vater associated with a neurofibromatosis type 1: a case report and review of the literature. JOP 11:64-8PubMed
187.
go back to reference Robinson MF, Furst EJ, Nunziata V et al (1992) Characterization of the clinical features of five families with hereditary primary cutaneous lichen amyloidosis and multiple endocrine neoplasia type 2. Henry Ford Hosp Med J 40:249-52PubMed Robinson MF, Furst EJ, Nunziata V et al (1992) Characterization of the clinical features of five families with hereditary primary cutaneous lichen amyloidosis and multiple endocrine neoplasia type 2. Henry Ford Hosp Med J 40:249-52PubMed
190.
go back to reference Donovan DT, Levy ML, Furst EJ et al (1989) Familial cutaneous lichen amyloidosis in association with multiple endocrine neoplasia type 2A: a new variant. Henry Ford Hosp Med J 37:147-50PubMed Donovan DT, Levy ML, Furst EJ et al (1989) Familial cutaneous lichen amyloidosis in association with multiple endocrine neoplasia type 2A: a new variant. Henry Ford Hosp Med J 37:147-50PubMed
207.
go back to reference Cameselle-Teijeiro J and Chan JK (1999) Cribriform-morular variant of papillary carcinoma: a distinctive variant representing the sporadic counterpart of familial adenomatous polyposis-associated thyroid carcinoma? Mod Pathol 12:400-11PubMed Cameselle-Teijeiro J and Chan JK (1999) Cribriform-morular variant of papillary carcinoma: a distinctive variant representing the sporadic counterpart of familial adenomatous polyposis-associated thyroid carcinoma? Mod Pathol 12:400-11PubMed
216.
go back to reference Stratakis CA and Raygada M (1993) Carney Complex. GeneReviews((R)) Stratakis CA and Raygada M (1993) Carney Complex. GeneReviews((R))
219.
go back to reference Ishikawa Y, Sugano H, Matsumoto T, Furuichi Y, Miller RW and Goto M (1999) Unusual features of thyroid carcinomas in Japanese patients with Werner syndrome and possible genotype-phenotype relations to cell type and race. Cancer 85:1345-52CrossRefPubMed Ishikawa Y, Sugano H, Matsumoto T, Furuichi Y, Miller RW and Goto M (1999) Unusual features of thyroid carcinomas in Japanese patients with Werner syndrome and possible genotype-phenotype relations to cell type and race. Cancer 85:1345-52CrossRefPubMed
232.
go back to reference Gasior-Perczak D, Kowalik A, Walczyk A et al (2019) Coexisting Germline CHEK2 and Somatic BRAF(V600E) Mutations in Papillary Thyroid Cancer and Their Association with Clinicopathological Features and Disease Course. Cancers (Basel) 11 https://doi.org/10.3390/cancers11111744 Gasior-Perczak D, Kowalik A, Walczyk A et al (2019) Coexisting Germline CHEK2 and Somatic BRAF(V600E) Mutations in Papillary Thyroid Cancer and Their Association with Clinicopathological Features and Disease Course. Cancers (Basel) 11 https://​doi.​org/​10.​3390/​cancers11111744
234.
243.
go back to reference Neurofibromatosis (1988) Conference statement. National Institutes of Health Consensus Development Conference. Arch Neurol 45:575–8. PMID: 3128965 Neurofibromatosis (1988) Conference statement. National Institutes of Health Consensus Development Conference. Arch Neurol 45:575–8. PMID: 3128965
250.
271.
go back to reference Gasior-Perczak D, Kowalik A, Gruszczynski K et al (2021) Incidence of the CHEK2 Germline Mutation and Its Impact on Clinicopathological Features, Treatment Responses, and Disease Course in Patients with Papillary Thyroid Carcinoma. Cancers (Basel) 13 https://doi.org/10.3390/cancers13030470 Gasior-Perczak D, Kowalik A, Gruszczynski K et al (2021) Incidence of the CHEK2 Germline Mutation and Its Impact on Clinicopathological Features, Treatment Responses, and Disease Course in Patients with Papillary Thyroid Carcinoma. Cancers (Basel) 13 https://​doi.​org/​10.​3390/​cancers13030470
Metadata
Title
Overview of the 2022 WHO Classification of Familial Endocrine Tumor Syndromes
Authors
Vania Nosé
Anthony Gill
José Manuel Cameselle Teijeiro
Aurel Perren
Lori Erickson
Publication date
01-03-2022
Publisher
Springer US
Published in
Endocrine Pathology / Issue 1/2022
Print ISSN: 1046-3976
Electronic ISSN: 1559-0097
DOI
https://doi.org/10.1007/s12022-022-09705-5

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