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13.12.2023 | ORIGINAL ARTICLE

Nasal and sinonasal tumors formed by atypical adenomatous lesions arising in respiratory epithelial adenomatoid hamartoma/seromucinous hamartoma

verfasst von: Michal Michal, Alena Skálová, Martin Hyrcza, Jan Laco, Tomáš Vaněček, Niels J. Rupp, Michael Michal, Květoslava Michalová, Abbas Agaimy, Martina Bradová

Erschienen in: Virchows Archiv | Ausgabe 1/2024

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Abstract

Two benign adenomatous lesions are commonly recognized within the sinonasal tract, namely respiratory epithelial adenomatoid hamartoma (REAH) and seromucinous hamartoma (SH). We present 10 hitherto unrecognized benign polypoid nasal and sinonasal tumoriform lesions having in average 3.6 cm in largest dimension, which are histogenetically related to SH and REAH. In addition to typical structures of REAH and SH, these lesions contained an additional characteristic and slightly atypical adenomatous component, which we termed atypical sinonasal glands arising in SH (ASGSH). ASGSH often produced deep red colored secretion with peripheral clearing similar to that seen in thyroid follicles. In contrast to SH, ASGSH was endowed by both secretory and myoepithelial layers and had mostly angulated shapes with snout-like protrusions into the lumens. Both layers were formed by an irregular, disorganized, and often incomplete cell lining, which had slightly atypical cytological features without mitoses. In 3 cases, ASGSHs revealed sebaceous differentiation, and in 3 cases the stroma produced a well-differentiated cartilage. Neoplastic nature of ASGSH was supported by finding of various mutations as revealed by next generation sequencing in five cases. In two cases each, we found identical mutations in BRAF gene (Val600Glu), and RET gene (Arg912Trp), respectively and in one case FAT1 gene alteration (Pro1665Leu).
Literatur
1.
Zurück zum Zitat Wenig BM, Heffner DK (1995) Respiratory epithelial adenomatoid hamartomas of the sinonasal tract and nasopharynx” A clinicopathologic study of 31 cases. Ann Otol Rhinol Laryngol 121:2706–2709 Wenig BM, Heffner DK (1995) Respiratory epithelial adenomatoid hamartomas of the sinonasal tract and nasopharynx” A clinicopathologic study of 31 cases. Ann Otol Rhinol Laryngol 121:2706–2709
2.
Zurück zum Zitat Weinreb I, Gnepp DR, Laver NM, Hoschar AP, Hunt JI, Seethala RR, Barnes EL, Chetty R, Perez-Ordonez R (2009) Seromucinous hamartomas: a clinicopathological study of a sinonasal glandular lesion lacking myoepithelial layer. Histopathology 54:205–211CrossRefPubMed Weinreb I, Gnepp DR, Laver NM, Hoschar AP, Hunt JI, Seethala RR, Barnes EL, Chetty R, Perez-Ordonez R (2009) Seromucinous hamartomas: a clinicopathological study of a sinonasal glandular lesion lacking myoepithelial layer. Histopathology 54:205–211CrossRefPubMed
3.
Zurück zum Zitat Baillie EE, Batsakis JG (1974) Glandular (seromucinous) hamartoma of the nasopharynx. Oral Surg Oral Med Oral Pathol 38:760–762CrossRefPubMed Baillie EE, Batsakis JG (1974) Glandular (seromucinous) hamartoma of the nasopharynx. Oral Surg Oral Med Oral Pathol 38:760–762CrossRefPubMed
5.
Zurück zum Zitat Ozolek JA, Hunt JL (2006) Tumor suppressor gene alterations in respiratory epithelial adenomatoid hamartoma (REAH) comparison to sinonasal adenocarcinoma and inflamed sinonasal mucosa. Am J Surg Pathol 30:1576–1580CrossRefPubMed Ozolek JA, Hunt JL (2006) Tumor suppressor gene alterations in respiratory epithelial adenomatoid hamartoma (REAH) comparison to sinonasal adenocarcinoma and inflamed sinonasal mucosa. Am J Surg Pathol 30:1576–1580CrossRefPubMed
6.
Zurück zum Zitat Ambrosini-Spaltro A, Morandi L, Spagnolo DV, Cavazza A, Brisigotti M, Damiani S, Jain S, Eusebi V (2010) Nasal seromucinous hamartoma (microglandular adenosis of the nose): a morphological and molecular study of five cases. Virchows Arch 457:727–734CrossRefPubMed Ambrosini-Spaltro A, Morandi L, Spagnolo DV, Cavazza A, Brisigotti M, Damiani S, Jain S, Eusebi V (2010) Nasal seromucinous hamartoma (microglandular adenosis of the nose): a morphological and molecular study of five cases. Virchows Arch 457:727–734CrossRefPubMed
7.
Zurück zum Zitat Skálová A, Baněčková M, Laco J, Di Palma S, Agaimy A, Ptáková N, Costes-Martineau V, Petersson BF, van den Hout MFCM, de Rezende G, Klubíčková N, Koblížek M, Koshyk O (2022) Sclerosing polycystic adenoma of salivary glands: a novel neoplasm characterized by PI3K-AKT pathway alterations-new insights into a challenging entity. Am J Surg Pathol 46:268–280CrossRefPubMed Skálová A, Baněčková M, Laco J, Di Palma S, Agaimy A, Ptáková N, Costes-Martineau V, Petersson BF, van den Hout MFCM, de Rezende G, Klubíčková N, Koblížek M, Koshyk O (2022) Sclerosing polycystic adenoma of salivary glands: a novel neoplasm characterized by PI3K-AKT pathway alterations-new insights into a challenging entity. Am J Surg Pathol 46:268–280CrossRefPubMed
8.
Zurück zum Zitat Donati M, Kastnerova L, Martinek P, Grossmann P, Sticová E, Hadravský L, Torday T, Kyclova J, Michal M, Kazakov DV (2020) Spitz tumors with ROS1 fusions: a clinicopathological study of 6 cases, including FISH for chromosomal copy number alterations and mutation analysis using next-generation sequencing. Am J Dermatopathol 42:92–102CrossRefPubMed Donati M, Kastnerova L, Martinek P, Grossmann P, Sticová E, Hadravský L, Torday T, Kyclova J, Michal M, Kazakov DV (2020) Spitz tumors with ROS1 fusions: a clinicopathological study of 6 cases, including FISH for chromosomal copy number alterations and mutation analysis using next-generation sequencing. Am J Dermatopathol 42:92–102CrossRefPubMed
9.
Zurück zum Zitat Michal M, Rubin BP, Kazakov DV, Michalová K, Šteiner P, Grossmann P, Hájková V, Martínek P, Švajdler M, Agaimy A, Hadravský L, Kalmykova AV, Konishi E, Heidenreich F, Michal M (2020) Inflammatory leiomyosarcoma shows frequent co-expression of smooth and skeletal muscle markers supporting a primitive myogenic phenotype: a report of 9 cases with a proposal for reclassification as low-grade inflammatory myogenic tumor. Virchows Arch 477:219–230CrossRefPubMed Michal M, Rubin BP, Kazakov DV, Michalová K, Šteiner P, Grossmann P, Hájková V, Martínek P, Švajdler M, Agaimy A, Hadravský L, Kalmykova AV, Konishi E, Heidenreich F, Michal M (2020) Inflammatory leiomyosarcoma shows frequent co-expression of smooth and skeletal muscle markers supporting a primitive myogenic phenotype: a report of 9 cases with a proposal for reclassification as low-grade inflammatory myogenic tumor. Virchows Arch 477:219–230CrossRefPubMed
10.
Zurück zum Zitat Skalova A, Sar A, Laco J, Metelkova A, Miesbauerova M, Steiner P, Michal M (2018) The role of SATB2 as a diagnostic marker of sinonasal intestinal-type adenocarcinoma. Appl Immunohistochem Mol Morphol 26:140–146CrossRefPubMed Skalova A, Sar A, Laco J, Metelkova A, Miesbauerova M, Steiner P, Michal M (2018) The role of SATB2 as a diagnostic marker of sinonasal intestinal-type adenocarcinoma. Appl Immunohistochem Mol Morphol 26:140–146CrossRefPubMed
11.
Zurück zum Zitat Sjősted S, Schmid AY, Vieira FG, Woller NC, Nielsen FC, von Buchwald C (2021) Intestinal metaplasia is a precursor lesion of sinonasal intestinal-type adenocarcinoma: genomic investigation of a case proving this hypothesis. APMIS 130:53–56CrossRef Sjősted S, Schmid AY, Vieira FG, Woller NC, Nielsen FC, von Buchwald C (2021) Intestinal metaplasia is a precursor lesion of sinonasal intestinal-type adenocarcinoma: genomic investigation of a case proving this hypothesis. APMIS 130:53–56CrossRef
12.
Zurück zum Zitat Jo VY, Mills SE, Cathro HP, Carson DL, Stelow EB (2009) Low-grade sinonasal adenocarcinomas. The association with and distinction from respiratory epithelial adenomatoid hamartomas and other glandular lesions. Am J Surg Pathol 33:401–408CrossRefPubMed Jo VY, Mills SE, Cathro HP, Carson DL, Stelow EB (2009) Low-grade sinonasal adenocarcinomas. The association with and distinction from respiratory epithelial adenomatoid hamartomas and other glandular lesions. Am J Surg Pathol 33:401–408CrossRefPubMed
13.
Zurück zum Zitat Skalova A, Cardesa A, Pfaltz M, Leivo I, Ryska A, Simpson R, Michal M (2003) Sinonasal tubulopapillary low grade adenocarcinoma. Histopathological, immunohistochemical and ultrastructural characterization of poorly recognized entity. Virchows Arch 443:152–158CrossRefPubMed Skalova A, Cardesa A, Pfaltz M, Leivo I, Ryska A, Simpson R, Michal M (2003) Sinonasal tubulopapillary low grade adenocarcinoma. Histopathological, immunohistochemical and ultrastructural characterization of poorly recognized entity. Virchows Arch 443:152–158CrossRefPubMed
14.
Zurück zum Zitat Luna MA (2005) Sinonasal tubulopapillary low-grade adenocarcinoma: a specific diagnosis or just another seromucous adenocarcinoma? Adv Anat Pathol 12:109–115CrossRefPubMed Luna MA (2005) Sinonasal tubulopapillary low-grade adenocarcinoma: a specific diagnosis or just another seromucous adenocarcinoma? Adv Anat Pathol 12:109–115CrossRefPubMed
15.
Zurück zum Zitat Rooper LM, Thompson LDR, Gagan J, Hwang JSG, London NR, Mikula MW, Stevens TM, Bishop JA (2022) Low-grade non-intestinal-type sinonasal adenocarcinoma: a histologically distinctive but molecularly heterogeneous entity. Modern Pathol 35:1160–1167CrossRef Rooper LM, Thompson LDR, Gagan J, Hwang JSG, London NR, Mikula MW, Stevens TM, Bishop JA (2022) Low-grade non-intestinal-type sinonasal adenocarcinoma: a histologically distinctive but molecularly heterogeneous entity. Modern Pathol 35:1160–1167CrossRef
16.
Zurück zum Zitat Purgina B, Bastaki JM, Duvvuri U, Seethaqla RR (2015) A subset of sinonasal non-intestinal type adenocarcinomas are truly seromucinous adenocarcinomas: a morphologic and immunophenotypic assessment and description of a novel pitfall. Head Neck Pathol 9:436–446CrossRefPubMedPubMedCentral Purgina B, Bastaki JM, Duvvuri U, Seethaqla RR (2015) A subset of sinonasal non-intestinal type adenocarcinomas are truly seromucinous adenocarcinomas: a morphologic and immunophenotypic assessment and description of a novel pitfall. Head Neck Pathol 9:436–446CrossRefPubMedPubMedCentral
17.
Zurück zum Zitat Abdullgaffar B, Hamadi I (2023) Are focal complex proliferations in respiratory adenomatoid/seromucinous hamartomas clues of precursor neoplastic lesions to sinonasal adenocarcinoma? Int J Surg Pathol 31:343–347CrossRefPubMed Abdullgaffar B, Hamadi I (2023) Are focal complex proliferations in respiratory adenomatoid/seromucinous hamartomas clues of precursor neoplastic lesions to sinonasal adenocarcinoma? Int J Surg Pathol 31:343–347CrossRefPubMed
19.
Zurück zum Zitat Baněčková M, Michal M, Laco J, Leivo I, Ptáková N, Horáková M, Michal M, Skálová A (2020) Immunohistochemical and genetic analysis of respiratory epithelial adenomatoid aamartomas and seromucinous hamartomas: are they precursor lesions to sinonasal low-grade tubulopapillary adenocarcinomas? Human Pathol 97:94–102CrossRef Baněčková M, Michal M, Laco J, Leivo I, Ptáková N, Horáková M, Michal M, Skálová A (2020) Immunohistochemical and genetic analysis of respiratory epithelial adenomatoid aamartomas and seromucinous hamartomas: are they precursor lesions to sinonasal low-grade tubulopapillary adenocarcinomas? Human Pathol 97:94–102CrossRef
20.
Zurück zum Zitat Dai J, Kunder CA, Chu EY, Chan EF, Egan CL, Novoa RA (2017) Development of RET mutant cutaneous angiosarcoma during BRAF inhibitor therapy. J Cutan Pathol 44:1053–1056CrossRefPubMed Dai J, Kunder CA, Chu EY, Chan EF, Egan CL, Novoa RA (2017) Development of RET mutant cutaneous angiosarcoma during BRAF inhibitor therapy. J Cutan Pathol 44:1053–1056CrossRefPubMed
21.
Zurück zum Zitat Kwok ALM, Tang AHN, Luk ISC, Lau GTC, Cheuk W (2023) Adenofibromatous solitary fibrous tumor: an unusual morphologic variant occurring in the sinonasal tract. Head and Neck Pathol 17:165–171CrossRef Kwok ALM, Tang AHN, Luk ISC, Lau GTC, Cheuk W (2023) Adenofibromatous solitary fibrous tumor: an unusual morphologic variant occurring in the sinonasal tract. Head and Neck Pathol 17:165–171CrossRef
22.
Zurück zum Zitat Shirakura T, Yamada Y, Nakata S, Asayama B, Seo Y, Tanikawa S, Kato T, Komoribayashi N, Kubo N, Monma N, Okura N, Tanaka S, Oda Y, Hirato J, Yokoo H, Nobusawa S (2022) Analysis of clinicopathological features and NAB2-STAT6 fusion variants of meningeal solitary fibrous tumor with ectopic salivary gland components in the cerebellopontine angle. Virchovs Arch 481:913–923CrossRef Shirakura T, Yamada Y, Nakata S, Asayama B, Seo Y, Tanikawa S, Kato T, Komoribayashi N, Kubo N, Monma N, Okura N, Tanaka S, Oda Y, Hirato J, Yokoo H, Nobusawa S (2022) Analysis of clinicopathological features and NAB2-STAT6 fusion variants of meningeal solitary fibrous tumor with ectopic salivary gland components in the cerebellopontine angle. Virchovs Arch 481:913–923CrossRef
23.
Zurück zum Zitat Javadirad E, Azimivaghar J, Montazer S, Sharafi S (2022) A systematic review of nasal chondromesenchymal hamartoma (NCMH) with a new case report. Head Neck Pathol 16:1172–1184CrossRefPubMedPubMedCentral Javadirad E, Azimivaghar J, Montazer S, Sharafi S (2022) A systematic review of nasal chondromesenchymal hamartoma (NCMH) with a new case report. Head Neck Pathol 16:1172–1184CrossRefPubMedPubMedCentral
24.
Zurück zum Zitat González IA, Stewart DG, Schultz KAP, Field AP, Hill DA, Dehner LP (2022) DICER1 tumor predisposition syndrome: an evolving story initiated with the pleuropulmonary blastoma. Modern Pathol 35:4–22CrossRef González IA, Stewart DG, Schultz KAP, Field AP, Hill DA, Dehner LP (2022) DICER1 tumor predisposition syndrome: an evolving story initiated with the pleuropulmonary blastoma. Modern Pathol 35:4–22CrossRef
Metadaten
Titel
Nasal and sinonasal tumors formed by atypical adenomatous lesions arising in respiratory epithelial adenomatoid hamartoma/seromucinous hamartoma
verfasst von
Michal Michal
Alena Skálová
Martin Hyrcza
Jan Laco
Tomáš Vaněček
Niels J. Rupp
Michael Michal
Květoslava Michalová
Abbas Agaimy
Martina Bradová
Publikationsdatum
13.12.2023
Verlag
Springer Berlin Heidelberg
Erschienen in
Virchows Archiv / Ausgabe 1/2024
Print ISSN: 0945-6317
Elektronische ISSN: 1432-2307
DOI
https://doi.org/10.1007/s00428-023-03719-y

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