• Mgr. Petr Martínek, Ph.D.
    Mgr. Petr Martínek, Ph.D.

Seznam publikací

  1. Ambrozkiewicz, F., Ali, E., Bradova, M., Slavík, P., Martinek, P., Svaton, M., Hemminki, A., & Hemminki, K. (2026). Mutational landscape of lung adenocarcinoma in Czechia. Cancer Treatment and Research Communications, 101095. 10.1016/j.ctarc.2026.101095
  2. Bradová, M., Slavík, P., Vaněček, T., Martínek, P., Grossmann, P., Kormunda, S., Behenská, K., Svatoň, M., Pešek, M., & Jirásek, T. (2026). Clinicopathologic features of KRAS G12C-mutated non-small cell lung carcinomas: Insights from 279 retrospective cases. Virchows Archiv, 1–15. 10.1007/s00428-026-04526-x
  3. Farkas, M., Agaimy, A., Švajdler, M., Hauer, L., Martínek, P., Vaněček, T., Pivovarčíková, K., Prchlíková, B., Simpson, R. H., & Gočárová, K. (2026). SMARCA4-deficient carcinoma of the head and neck region: Report of 8 new sinonasal and non-sinonasal cases and literature review. Virchows Archiv, 1–17. 10.1007/s00428-026-04459-5
  4. Gettse, P., Presl, J., Martinek, P., Peterikova, A. S., Michal, M., & Michalova, K. (2026). A subset of low-grade TP53-mutated endometrial carcinomas exhibits a copy-number-low profile and favorable outcomes, challenging current high-risk classification. International Journal of Gynecological Cancer, 36(2). 10.1016/j.ijgc.2025.103535
  5. Michal, M., Malik, F., Mansour, B., Hattery, T., Dehner, C. A., Martínek, P., Hájková, V., Vaněček, T., Chrisinger, J. S., & Machado, I. (2026). FET-Rearranged Myoepithelial Tumors Are Clinically Heterogeneous and Epigenetically Distinct from PLAG1-Rearranged Adnexal and Salivary Gland Myoepithelial Tumors. Clinical Cancer Research, 32(3), 628–644. 10.1158/1078-0432.CCR-25-2426
  6. Michalova, K., Hruby, M., Baniak, N., Gordetsky, J. B., Idrees, M. T., Anderson, W. J., Martinek, P., Grendar, M., Michal, M., & Ulbright, T. M. (2026). Genome-Wide Copy-Number Landscape of Germ Cell Tumors With Synchronous Conventional and “Somatic-Type” Malignancy Components. The American Journal of Surgical Pathology, 50(5), 535–542. 10.1097/pas.0000000000002515
  7. Bradová, M., Agaimy, A., Laco, J., Martínek, P., Ing, S. K., Badoual, C., Damjanov, I., Leivo, I., Bacchi, C. E., & Comperat, E. (2025). Sinonasal adenoid cystic carcinomas accompanied by seromucinous hamartoma and/or atypical sinonasal glands arising from seromucinous hamartoma: Insight into their histogenesis. Virchows Archiv, 486(6), 1269–1287. 10.1007/s00428-025-04053-1
  8. de Lima-Souza, R. A., de Carvalho Kimura, T., Scarini, J. F., Lavareze, L., Maciel, T. F., Damas, I. I., Hara, L. W., de Sousa Mesquita, A., Simionato, A. V. C., & Martínek, P. (2025). Discovery metabolomics and genetic analysis reveal lipid pathway alterations associated with malignant phenotype acquisition in pleomorphic adenoma and a novel NTF3: ITPR2 fusion in carcinoma ex pleomorphic adenoma. Virchows Archiv, 1–13. 10.1007/s00428-025-04242-y
  9. Jäger, N., Reuss, D. E., Sill, M., Schrimpf, D., Suwala, A. K., Sievers, P., Banan, R., Hinz, F., Rahmanzade, R., & Bogumil, H. (2025). Advancing sarcoma diagnostics with expanded DNA methylation-based classification. medRxiv. 10.1101/2025.06.30.25330543
  10. Koleják, R., Mraček, J., Šubrt, I., Vaněček, T., Martínek, P., Mezencev, R., Farcas, M., Švajdler, M., & Přibáň, V. (2025). Primary Intracranial Sarcoma, DICER1-Mutant, Diagnosed by DNA Methylation Profiling in an Adult Patient with Germline DICER1 Mutation: A Case Report. International Journal of Surgical Pathology, 10668969251388390. 10.1177/10668969251388390
  11. Michalova, K., Martinek, P., Mezencev, R., Gupta, S., Williamson, S., Wasco, M., Mohanty, S., Magi-Galluzzi, C., Cañete-Portillo, S., & Aron, M. (2025). Renal juxtaglomerular cell tumors exhibit distinct genomic and epigenomic features and lack recurrent gene fusions: Comprehensive molecular analysis of a multi-institutional series. The American Journal of Surgical Pathology, 49(3), 217–226. 10.1097/pas.0000000000002344
  12. Ondič, O., Michalová, K., Švajdler, M., Presl, J., Kosťun, J., Hájková, V., Martínek, P., & Michal, M. (2025). Molecular substratification of endometrial carcinomas with no special molecular profile (NSMP) by using a limited NGS custom panel may facilitate effective patient selection for the PIK3CA-targeted therapy. Virchows Archiv, 486(4), 827–832. 10.1007/s00428-024-03905-6
  13. Pancsa, T., Martínek, P., & Michal, M. (2025). Malignant esophageal glomus tumor with CARMN:: NOTCH2 fusion: An additional tumor underscoring the frequent tendency of esophageal glomus tumors for aggressive behavior. International journal of surgical pathology, 33(4), 987–991. 10.1177/10668969241291887
  14. Sangoi, A. R., Pivovarcikova, K., Akgul, M., Williamson, S. R., Ulamec, M., Rogala, J. D., Martinek, P., Vanecek, T., Hes, O., & Alaghehbandan, R. (2025). Chromophobe renal cell carcinoma with extensive retraction artifact: A potential diagnostic pitfall from micropapillary urothelial carcinoma. International Journal of Surgical Pathology, 33(1), 5–12. 10.1177/10668969241239678
  15. Skálová, A., Bradová, M., Agaimy, A., Laco, J., Badual, C., Ihrler, S., Damjanov, I., Rupp, N. J., Bacchi, C. E., & Mueller, S. (2025). Molecular profiling of sinonasal adenoid cystic carcinoma: Canonical and noncanonical gene fusions and mutation. The American Journal of Surgical Pathology, 49(3), 227–242. 10.1097/pas.0000000000002349
  16. Skálová, A., Bradová, M., Laco, J., Vaněček, T., Hájková, V., Martínek, P., Grendár, M., Querzoli, G., Leivo, I., & Michal, M. (2025). Basal cell adenoma with S100 protein–positive “stroma”: A distinct triphasic salivary gland neoplasm characterized by CTNNB1 mutation. Virchows Archiv, 1–18. 10.1007/s00428-025-04141-2
  17. Strakova-Peterikova, A., Fedeli, F., Rychly, B., Soukup, J., Michal, M., Martinek, P., Grendar, M., Mosaieby, E., Ptakova, N., & Slisarenko, M. (2025). Calcifying nested stromal-epithelial tumor of the liver: Report of two cases revealing novel WT1 mutation and distinct epigenetic features. Virchows Archiv, 1–10. 10.1007/s00428-025-04281-5
  18. Švajdler, M., Brousil, M., Soukup, J., Netuka, D., Kašparová, P., Rychlý, B., Jirásek, T., Hendrych, M., Farcas, M., & Pivovarčíková, K. (2025). Glycoprotein nonmetastatic melanoma protein b immunohistochemistry can be a useful ancillary tool to diagnose subependymal giant cell astrocytoma. Virchows Archiv, 1–9. 10.1007/s00428-025-04110-9
  19. Klubíčková, N., Dermawan, J. K., Mosaieby, E., Martínek, P., Vaněček, T., Hájková, V., Ptáková, N., Grossmann, P., Šteiner, P., & Švajdler, M. (2024). Comprehensive clinicopathological, molecular, and methylation analysis of mesenchymal tumors with NTRK and other kinase gene aberrations. The Journal of Pathology, 263(1), 61–73. 10.1002/path.6260
  20. Mickael, M.-E., Kubick, N., Atanasov, A. G., Martinek, P., Horbańczuk, J. O., Floretes, N., Michal, M., Vanecek, T., Paszkiewicz, J., & Sacharczuk, M. (2024). Using copy number variation data and neural networks to predict cancer metastasis origin achieves high area under the curve value with a trade-off in precision. Current Issues in Molecular Biology, 46(8), 8301–8319. 10.3390/cimb46080490
  21. Michal, M., Agaimy, A., Croce, S., Mechtersheimer, G., Gross, J. M., Xing, D., Bell, D. A., Gupta, S., Mosaieby, E., & Martínek, P. (2024). PLAG1-rearranged uterine sarcomas: A study of 11 cases showing a wide phenotypical spectrum not limited to myxoid leiomyosarcoma-like morphology. Modern Pathology, 37(9), 100552. 10.1016/j.modpat.2024.100552
  22. Sánta, F., Dabaghian, A., Pósfai, B., Vasas, B., Kaizer, L., Jenei, A., Scheich, B., Téglási, V., Sápi, Z., & Bíró, K. (2024). Morphological diversity in SDH-deficient renal carcinomas: A three-case exploration of variant features and dedifferentiation. Virchows Archiv, 485(6), 1167–1173. 10.1007/s00428-024-03978-3
  23. Skálová, A., Klubíčková, N., Bradová, M., Agaimy, A., Rupp, N. J., Damjanov, I., Kolnikova, G., Martínek, P., Šteiner, P., & Grossmann, P. (2024). Discovery of novel TULP4/ACTN4/EWSR1/ACTB:: MYB and ESRRG:: DNM3 fusions expands molecular landscape of adenoid cystic carcinoma beyond fusions between MYB/MYBL1 and NFIB genes. The American Journal of Surgical Pathology, 48(12), 1503–1511. 10.1097/pas.0000000000002304
  24. Kalmykova, A., Mosaieby, E., Kacerovská, D., Baranovska-Andrigo, V., Martínek, P., Smahová, S., Michal, M., & Michal, M. (2023). MITF:: CREM-rearranged tumor: A novel group of cutaneous tumors with melanocytic differentiation. Virchows Archiv, 483(4), 569–575. 10.1007/s00428-023-03621-7
  25. Michal, M., Kravtsov, O., Ross, J. S., Skanderová, D., Martínek, P., Mosaieby, E., Mata, D. A., Williams, E. A., & Hung, Y. P. (2023). Clear cell mesotheliomas with inactivating VHL mutations and near‐haploid genomic features. Genes, Chromosomes and Cancer, 62(5), 267–274. 10.1002/gcc.23119
  26. Warmke, L. M., Michal, M., Martínek, P., Agaimy, A., Din, N. U., Perret, R., Hostein, I., Le Loarer, F., Voltaggio, L., & Gross, J. M. (2023). “PRRX1-rearranged mesenchymal tumors”: Expanding the immunohistochemical profile and molecular spectrum of a recently described entity with the proposed revision of nomenclature. Virchows Archiv, 483(2), 207–214. 10.1007/s00428-023-03575-w
  27. Donati, M., Martinek, P., Steiner, P., Grossmann, P., Vanecek, T., Kastnerova, L., Kolm, I., Baneckova, M., Donati, P., & Kletskaya, I. (2022). Novel insights into the BAP1-inactivated melanocytic tumor. Modern Pathology, 35(5), 664–675. 10.1038/s41379-021-00976-7
  28. Grendár, M., Martínek, P., Loderer, D., & Ondič, O. (2022). CNHplus: The chromosomal copy number heterogeneity which respects biological constraints. BioRxiv, 2022–09. 10.1101/2022.09.30.510279
  29. Mosaieby, E., Martínek, P., & Ondič, O. (2022). The significance of the fusion partner gene genomic neighborhood analysis in translocation‐defined tumors. Molecular Genetics & Genomic Medicine, 10(8), e1994. 10.1002/mgg3.1994
  30. Nemcova, J., Riegert, J., Cerna, K., Rob, F., Smahelova, J., Hercogova, J. T., Martinek, P., & Ondic, O. (2022a). Prevalence of oral and anal human papillomavirus infection in Czech predominantly HIV-positive men having sex with men-data from a previously unreported population. International journal of STD & AIDS, 33(12), 1054–1064. 10.1177/09564624221123869
  31. Nemcova, J., Riegert, J., Cerna, K., Rob, F., Smahelova, J., Hercogova, J. T., Martinek, P., & Ondic, O. (2022b). Prevalence of oral and anal human papillomavirus infection in Czech predominantly Human immunodeficiency virus-positive men having sex with men-data from a previously unreported population. International Journal of STD & AIDS. 10.1177/09564624221123869
  32. Polivka, J., Svajdler, M., Priban, V., Mracek, J., Kasik, P., Martinek, P., Ptakova, N., Bagheri, M. S., Shetti, D., & Pesta, M. (2022). Oncogenic fusions in gliomas: An institutional experience. Anticancer Research, 42(4), 1933–1939. 10.21873/anticanres.15671
  33. Donati, M., Nosek, D., Waldenbäck, P., Martinek, P., Jonsson, B.-A., Galgonkova, P., Hawawrehova, M., Berouskova, P., Kastnerova, L., & Persichetti, P. (2021). MAP2K1-mutated melanocytic neoplasms with a SPARK-like morphology. The American Journal of Dermatopathology, 43(6), 412–417. 10.1097/dad.0000000000001840
  34. Ptáková, N., Martínek, P., Holubec, L., Janovský, V., Vančurová, J., Grossmann, P., Navarro, P. A., Rodriguez Moreno, J. F., Alaghehbandan, R., & Hes, O. (2021). Identification of tumors with NRG1 rearrangement, including a novel putative pathogenic UNC5D‐NRG1 gene fusion in prostate cancer by data‐drilling a de‐identified tumor database. Genes, Chromosomes and Cancer, 60(7), 474–481. 10.1002/gcc.22942
  35. Baněčková, M., Martínek, P., Skálová, A., Mezencev, R., Hadravský, L., Michal, M., & Švajdler, M. (2020). Solitary fibrous tumors of the head and neck region revisited: A single-institution study of 20 cases and review of the literature. Human Pathology, 99, 1–12. 10.1016/j.humpath.2020.03.007
  36. Donati, M., Kastnerova, L., Martinek, P., Grossmann, P., Sticová, E., Hadravský, L., Torday, T., Kyclova, J., Michal, M., & Kazakov, D. V. (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. The American Journal of Dermatopathology, 42(2), 92–102. 10.1097/dad.0000000000001499
  37. Donati, M., Martinek, P., Kastnerova, L., Persichetti, P., Michal, M., & Kazakov, D. V. (2020). RAF1 gene fusions as a possible driver mechanism in rare BAP1-inactivated melanocytic tumors: A report of 2 cases. The American Journal of Dermatopathology, 42(12), 961–966. 10.1097/dad.0000000000001740
  38. Kastnerova, L., Martinek, P., Grossmann, P., Steiner, P., Vanecek, T., Kyclova, J., Ferak, I., Zalud, R., Slehobr, O., & Svajdler, P. (2020). A clinicopathological study of 29 spitzoid melanocytic lesions with ALK fusions, including novel fusion variants, accompanied by fluorescence in situ hybridization analysis for chromosomal copy number changes, and both TERT promoter and next-generation sequencing mutation analysis. The American Journal of Dermatopathology, 42(8), 578–592. 10.1097/dad.0000000000001632
  39. Michal, M., Rubin, B. P., Kazakov, D. V., Michalová, K., Šteiner, P., Grossmann, P., Hájková, V., Martínek, P., Švajdler, M., & Agaimy, A. (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 Archiv, 477(2), 219–230. 10.1007/s00428-020-02774-z
  40. Michalova, K., McKenney, J. K., Kristiansen, G., Steiner, P., Grossmann, P., Putzova, M., Martinek, P., Chottova-Dvorakova, M., Michal, M., & Hes, O. (2020). Novel insights into the mixed germ cell-sex cord stromal tumor of the testis: Detection of chromosomal aneuploidy and further morphological evidence supporting the neoplastic nature of the germ cell component. Virchows Archiv, 477(5), 615–623. 10.1007/s00428-020-02843-3
  41. Pires-Luis, A. S., Martinek, P., Alaghehbandan, R., Trpkov, K., Comperat, E. M., Montiel, D. M. P., Bulimbasic, S., Lobo, J., Henrique, R., & Vanecek, T. (2020). Molecular genetic features of primary nonurachal enteric-type adenocarcinoma, urachal adenocarcinoma, mucinous adenocarcinoma, and intestinal metaplasia/adenoma: Review of the literature and next-generation sequencing study. Advances in anatomic pathology, 27(5), 303–310. 10.1097/pap.0000000000000268
  42. Polivka, J., Svajdler, M., Priban, V., Martinek, P., Ptakova, N., & Kasik, P. (2020). 386P Oncogenic fusions in CNS gliomas assessed by next generation sequencing: The real-world experience. Annals of Oncology, 31, S405–S406. 10.1016/j.annonc.2020.08.495
  43. Rogala, J., Kojima, F., Alaghehbandan, R., Agaimy, A., Martinek, P., Ondic, O., Ulamec, M., Sperga, M., Michalova, K., & Pivovarcikova, K. (2020). Papillary renal cell carcinoma with prominent spindle cell stroma-tumor mimicking mixed epithelial and stromal tumor of the kidney: Clinicopathologic, morphologic, immunohistochemical and molecular genetic analysis of 6 cases. Annals of Diagnostic Pathology, 44, 151441. 10.1016/j.anndiagpath.2019.151441
  44. Alaghehbandan, R., Ulamec, M., Martinek, P., Pivovarcikova, K., Michalova, K., Skenderi, F., Hora, M., Michal, M., & Hes, O. (2019). Papillary pattern in clear cell renal cell carcinoma: Clinicopathologic, morphologic, immunohistochemical and molecular genetic analysis of 23 cases. Annals of diagnostic pathology, 38, 80–86. 10.1016/j.anndiagpath.2018.11.004
  45. Gonzalez, M. L., Alaghehbandan, R., Pivovarcikova, K., Michalova, K., Rogala, J., Martinek, P., Foix, M. P., Mundo, E. C., Comperat, E., & Ulamec, M. (2019). Reactivity of CK 7 across the spectrum of renal cell carcinomas with clear cells. Histopathology, 74(4), 608–617. 10.1111/his.13791
  46. Kastnerova, L., Luzar, B., Goto, K., Grishakov, V., Gatalica, Z., Kamarachev, J., Martinek, P., Hájková, V., Grossmann, P., & Imai, H. (2019). Secretory Carcinoma of the Skin: Report of 6 Cases, Including a Case With a Novel: NFIX-PKN1: Translocation. The American journal of surgical pathology, 43(8), 1092–1098. 10.1097/PAS.0000000000001261
  47. Kojima, F., Bulimbasic, S., Alaghehbandan, R., Martinek, P., Vanecek, T., Michalova, K., Pivovarcikova, K., Michal, M., Hora, M., & Murata, S. (2019). Clear cell renal cell carcinoma with Paneth-like cells: Clinicopathologic, morphologic, immunohistochemical, ultrastructural, and molecular analysis of 13 cases. Annals of diagnostic pathology, 41, 96–101. 10.1016/j.anndiagpath.2019.05.012
  48. Michal, M., Ptáková, N., Martínek, P., Gatalica, Z., Kazakov, D. V., Michalová, K., Stoláriková, L., Švajdler, M., & Michal, M. (2019). S100 and CD34 positive spindle cell tumor with prominent perivascular hyalinization and a novel NCOA4‐RET fusion. Genes, Chromosomes and Cancer, 58(9), 680–685. 10.1002/gcc.22758
  49. Pivovarcikova, K., Agaimy, A., Martinek, P., Alaghehbandan, R., Perez‐Montiel, D., Alvarado‐Cabrero, I., Rogala, J., Kuroda, N., Rychly, B., & Gasparov, S. (2019). Primary renal well‐differentiated neuroendocrine tumour (carcinoid): Next‐generation sequencing study of 11 cases. Histopathology, 75(1), 104–117. 10.1111/his.13856
  50. Pivovarcikova, K., Martinek, P., Grossmann, P., Trpkov, K., Alaghehbandan, R., Magi-Galluzzi, C., Foix, M. P., Mundo, E. C., Berney, D., & Gill, A. (2019). Fumarate hydratase deficient renal cell carcinoma: Chromosomal numerical aberration analysis of 12 cases. Annals of Diagnostic Pathology, 39, 63–68. 10.1016/j.anndiagpath.2019.02.008
  51. Santana, T., Pavel, A., Martinek, P., Steiner, P., Grossmann, P., Baněčková, M., & Skálová, A. (2019). Biomarker immunoprofile and molecular characteristics in salivary duct carcinoma: Clinicopathological and prognostic implications. Human Pathology, 93, 37–47. 10.1016/j.humpath.2019.08.009
  52. Švajdler, M., Michal, M., Martínek, P., Ptáková, N., Kinkor, Z., Szépe, P., Švajdler, P., Mezencev, R., & Michal, M. (2019). Fibro-osseous pseudotumor of digits and myositis ossificans show consistent COL1A1-USP6 rearrangement: A clinicopathological and genetic study of 27 cases. Human Pathology, 88, 39–47. 10.1016/j.humpath.2019.02.009
  53. Trpkov, K., Williamson, S. R., Gao, Y., Martinek, P., Cheng, L., Sangoi, A. R., Yilmaz, A., Wang, C., San Miguel Fraile, P., & Perez Montiel, D. M. (2019). Low‐grade oncocytic tumour of kidney (CD117‐negative, cytokeratin 7‐positive): A distinct entity? Histopathology, 75(2), 174–184. 10.1111/his.13865
  54. He, H., Trpkov, K., Martinek, P., Isikci, O. T., Maggi-Galuzzi, C., Alaghehbandan, R., Gill, A. J., Tretiakova, M., Lopez, J. I., & Williamson, S. R. (2018). “High-grade oncocytic renal tumor”: Morphologic, immunohistochemical, and molecular genetic study of 14 cases. Virchows Archiv, 473(6), 725–738. 10.1007/s00428-018-2456-4
  55. Chapman, E., Skalova, A., Ptakova, N., Martinek, P., Goytain, A., Tucker, T., Xiong, W., Leader, M., Kudlow, B. A., & Haimes, J. D. (2018). Molecular profiling of hyalinizing clear cell carcinomas revealed a subset of tumors harboring a novel EWSR1-CREM fusion: Report of 3 cases. The American Journal of Surgical Pathology, 42(9), 1182–1189. 10.1097/pas.0000000000001114
  56. Kazakov, D. V., Kyrpychova, L., Martinek, P., Grossmann, P., Steiner, P., Vanecek, T., Pavlovsky, M., Bencik, V., Michal, M., & Michal, M. (2018). ALK gene fusions in epithelioid fibrous histiocytoma: A study of 14 cases, with new histopathological findings. The American Journal of Dermatopathology, 40(11), 805–814. 10.1097/dad.0000000000001085
  57. Kyrpychova, L., Vanecek, T., Grossmann, P., Martinek, P., Steiner, P., Hadravsky, L., Belousova, I. E., Shelekhova, K. V., Svajdler, M., & Dubinsky, P. (2018). Small subset of adenoid cystic carcinoma of the skin is associated with alterations of the MYBL1 gene similar to their extracutaneous counterparts. The American Journal of Dermatopathology, 40(10), 721–726. 10.1097/dad.0000000000001091
  58. Michal, M., Agaimy, A., Contreras, A. L., Svajdler, M., Kazakov, D. V., Steiner, P., Grossmann, P., Martinek, P., Hadravsky, L., & Michalova, K. (2018). Dysplastic Lipoma: A Distinctive Atypical Lipomatous Neoplasm With Anisocytosis, Focal Nuclear Atypia, p53 Overexpression, and a Lack of: MDM2: Gene Amplification by FISH: A Report of 66 Cases Demonstrating Occasional Multifocality and a Rare Association With Retinoblastoma. The American Journal of Surgical Pathology, 42(11), 1530–1540. 10.1097/pas.0000000000001129
  59. Michal, M., Berry, R. S., Rubin, B. P., Kilpatrick, S. E., Agaimy, A., Kazakov, D. V., Steiner, P., Ptakova, N., Martinek, P., & Hadravsky, L. (2018). EWSR1-SMAD3–rearranged fibroblastic tumor: An emerging entity in an increasingly more complex group of fibroblastic/myofibroblastic neoplasms. The American Journal of Surgical Pathology, 42(10), 1325–1333. 10.1097/PAS.0000000000001109
  60. Michalova, K., Steiner, P., Alaghehbandan, R., Trpkov, K., Martinek, P., Grossmann, P., Montiel, D. P., Sperga, M., Straka, L., & Prochazkova, K. (2018). Papillary renal cell carcinoma with cytologic and molecular genetic features overlapping with renal oncocytoma: Analysis of 10 cases. Annals of diagnostic pathology, 35, 1–6. 10.1016/j.anndiagpath.2018.01.010
  61. Petersson, F., Martinek, P., Vanecek, T., Pivovarcikova, K., Peckova, K., Ondic, O., Perez-Montiel, D., Skenderi, F., Ulamec, M., & Nenutil, R. (2018). Renal cell carcinoma with leiomyomatous stroma: A group of tumors with indistinguishable histopathologic features, but 2 distinct genetic profiles: Next-generation sequencing analysis of 6 cases negative for aberrations related to the VHL gene. Applied immunohistochemistry & molecular morphology, 26(3), 192–197. 10.1097/pai.0000000000000410
  62. Rotterova, P., Martinek, P., Alaghehbandan, R., Prochazkova, K., Damjanov, I., Rogala, J., Suster, S., Perez-Montiel, D., Alvarado-Cabrero, I., & Sperga, M. (2018). High-grade renal cell carcinoma with emperipolesis: Clinicopathological, immunohistochemical and molecular-genetic analysis of 14 cases. Histol Histopathol, 33(3), 277–287. 10.14670/HH-11-925
  63. Skalova, A., Vanecek, T., Martinek, P., Weinreb, I., Stevens, T. M., Simpson, R. H., Hyrcza, M., Rupp, N. J., Baneckova, M., & Michal Jr, M. (2018). Molecular profiling of mammary analog secretory carcinoma revealed a subset of tumors harboring a novel ETV6-RET translocation: Report of 10 cases. The American journal of surgical pathology, 42(2), 234–246. 10.1097/pas.0000000000000972
  64. Konstantinova, A. M., Vanecek, T., Martinek, P., Kyrpychova, L., Spagnolo, D. V., Stewart, C. J., Portelli, F., Michal, M., & Kazakov, D. V. (2017). Molecular alterations in lesions of anogenital mammary-like glands and their mammary counterparts including hidradenoma papilliferum, intraductal papilloma, fibroadenoma and phyllodes tumor. Annals of Diagnostic Pathology, 28, 12–18. 10.1016/j.anndiagpath.2017.02.004
  65. Kyrpychova, L., Carr, R. A., Martinek, P., Vanecek, T., Perret, R., Chottová-Dvořáková, M., Zamecnik, M., Hadravsky, L., Michal, M., & Kazakov, D. V. (2017). Basal cell carcinoma with matrical differentiation: Clinicopathologic, immunohistochemical, and molecular biological study of 22 cases. The American Journal of Surgical Pathology, 41(6), 738–749. 10.1097/pas.0000000000000841
  66. Peckova, K., Martinek, P., Pivovarcikova, K., Vanecek, T., Alaghehbandan, R., Prochazkova, K., Montiel, D. P., Hora, M., Skenderi, F., & Ulamec, M. (2017). Cystic and necrotic papillary renal cell carcinoma: Prognosis, morphology, immunohistochemical, and molecular-genetic profile of 10 cases. Annals of diagnostic pathology, 26, 23–30. 10.1016/j.anndiagpath.2016.10.007
  67. Ryška, A., Horký, O., Berkovcová, J., Tichá, I., Kalinová, M., Matějčková, M., Bóday, A., Drábek, J., Martínek, P., & Šimová, J. (2017a). Malignant melanoma-from classical histology towards molecular genetic testing. Klinicka onkologie: casopis Ceske a Slovenske Onkologicke Spolecnosti, 30(3), 182–189. 10.14735/amko2017182
  68. Skenderi, F., Ulamec, M., Vanecek, T., Martinek, P., Alaghehbandan, R., Foix, M. P., Babankova, I., Montiel, D. P., Alvarado-Cabrero, I., & Svajdler, M. (2017). Warthin-like papillary renal cell carcinoma: Clinicopathologic, morphologic, immunohistochemical and molecular genetic analysis of 11 cases. Annals of diagnostic pathology, 27, 48–56. 10.1016/j.anndiagpath.2017.01.005
  69. Foix, M. P., Dunatov, A., Martinek, P., Mundó, E. C., Suster, S., Sperga, M., Lopez, J. I., Ulamec, M., Bulimbasic, S., & Montiel, D. P. (2016). Morphological, immunohistochemical, and chromosomal analysis of multicystic chromophobe renal cell carcinoma, an architecturally unusual challenging variant. Virchows archiv, 469(6), 669–678. 10.1007/s00428-016-2022-x
  70. Harrison, W. J., Andrici, J., Maclean, F., Madadi-Ghahan, R., Farzin, M., Sioson, L., Toon, C. W., Clarkson, A., Watson, N., & Pickett, J. (2016). Fumarate hydratase–deficient uterine leiomyomas occur in both the syndromic and sporadic settings. The American journal of surgical pathology, 40(5), 599–607. 10.26226/morressier.596dfd56d462b80292387898
  71. Hes, O., Mundo, E. C., Peckova, K., Lopez, J. I., Martinek, P., Vanecek, T., Falconieri, G., Agaimy, A., Davidson, W., & Petersson, F. (2016). Biphasic squamoid alveolar renal cell carcinoma: A distinctive subtype of papillary renal cell carcinoma? The American Journal of Surgical Pathology, 40(5), 664–675. 10.1097/pas.0000000000000639
  72. Pivovarcikova, K., Peckova, K., Martinek, P., Montiel, D. P., Kalusova, K., Pitra, T., Hora, M., Skenderi, F., Ulamec, M., & Daum, O. (2016). “Mucin”-secreting papillary renal cell carcinoma: Clinicopathological, immunohistochemical, and molecular genetic analysis of seven cases. Virchows archiv, 469(1), 71–80. 10.1007/s00428-016-1936-7
  73. Trpkov, K., Hes, O., Agaimy, A., Bonert, M., Martinek, P., Magi-Galluzzi, C., Kristiansen, G., Lüders, C., Nesi, G., & Compérat, E. (2016). Fumarate hydratase–deficient renal cell carcinoma is strongly correlated with fumarate hydratase mutation and hereditary leiomyomatosis and renal cell carcinoma syndrome. The American journal of surgical pathology, 40(7), 865–875. 10.1097/PAS.0000000000000617
  74. Trpkov, K., Hes, O., Bonert, M., Lopez, J. I., Bonsib, S. M., Nesi, G., Comperat, E., Sibony, M., Berney, D. M., & Martinek, P. (2016). Eosinophilic, solid, and cystic renal cell carcinoma: Clinicopathologic study of 16 unique, sporadic neoplasms occurring in women. The American journal of surgical pathology, 40(1), 60–71. 10.1097/PAS.0000000000000508
  75. Ulamec, M., Skenderi, F., Zhou, M., Krušlin, B., Martínek, P., Grossmann, P., Peckova, K., Alvarado-Cabrero, I., Kalusova, K., & Kokoskova, B. (2016). Molecular genetic alterations in renal cell carcinomas with tubulocystic pattern: Tubulocystic renal cell carcinoma, tubulocystic renal cell carcinoma with heterogenous component and familial leiomyomatosis-associated renal cell carcinoma. Clinicopathologic and molecular genetic analysis of 15 cases. Applied immunohistochemistry & molecular morphology, 24(7), 521–530. 10.1097/pai.0000000000000213
  76. Hayes, M., Peckova, K., Martinek, P., Hora, M., Kalusova, K., Straka, L., Daum, O., Kokoskova, B., Rotterova, P., & Pivovarčikova, K. (2015). Molecular-genetic analysis is essential for accurate classification of renal carcinoma resembling Xp11. 2 translocation carcinoma. Virchows Archiv, 466(3), 313–322. 10.1007/s00428-014-1702-7
  77. Martínek, P., Grossmann, P., Hes, O., Bouda, J., Eret, V., Frizzell, N., Gill, A. J., & Ondič, O. (2015). Genetic testing of leiomyoma tissue in women younger than 30 years old might provide an effective screening approach for the hereditary leiomyomatosis and renal cell cancer syndrome (HLRCC). Virchows Archiv, 467(2), 185–191. 10.1007/s00428-015-1783-y
  78. Peckova, K., Martinek, P., Ohe, C., Kuroda, N., Bulimbasic, S., Mundo, E. C., Montiel, D. P., Lopez, J. I., Daum, O., & Rotterova, P. (2015). Chromophobe renal cell carcinoma with neuroendocrine and neuroendocrine-like features. Morphologic, immunohistochemical, ultrastructural, and array comparative genomic hybridization analysis of 18 cases and review of the literature. Annals of diagnostic pathology, 19(4), 261–268. 10.1016/j.anndiagpath.2015.05.001
  79. Peckova, K., Martinek, P., Sperga, M., Montiel, D. P., Daum, O., Rotterova, P., Kalusová, K., Hora, M., Pivovarcikova, K., & Rychly, B. (2015). Mucinous spindle and tubular renal cell carcinoma: Analysis of chromosomal aberration pattern of low-grade, high-grade, and overlapping morphologic variant with papillary renal cell carcinoma. Annals of diagnostic pathology, 19(4), 226–231. 10.1016/j.anndiagpath.2015.04.004
  80. Hes, O., De Souza, T. G., Pivovarcikova, K., Grossmann, P., Martinek, P., Kuroda, N., Kacerovska, D., Svajdler, M., Straka, L., & Petersson, F. (2014). Distinctive renal cell tumor simulating atrophic kidney with 2 types of microcalcifications. Report of 3 cases. Annals of Diagnostic Pathology, 18(2), 82–88. 10.1016/j.anndiagpath.2013.12.003
  81. Hes, O., Pivovarcikova, K., Stehlik, J., Martinek, P., Vanecek, T., Bauleth, K., Dolejsova, O., Petersson, F., Hora, M., & Montiel, D. P. (2014). Choriogonadotropin positive seminoma—A clinicopathological and molecular genetic study of 15 cases. Annals of diagnostic pathology, 18(2), 89–94. 10.1016/j.anndiagpath.2013.12.004
  82. Peckova, K., Vanecek, T., Martinek, P., Spagnolo, D., Kuroda, N., Brunelli, M., Vranic, S., Djuricic, S., Rotterova, P., & Daum, O. (2014). Aggressive and nonaggressive translocation t (6; 11) renal cell carcinoma: Comparative study of 6 cases and review of the literature. Annals of diagnostic pathology, 18(6), 351–357. 10.1016/j.anndiagpath.2014.10.002
  83. Petersson, F., Branzovsky, J., Martinek, P., Korabecna, M., Kruslin, B., Hora, M., Peckova, K., Bauleth, K., Pivovarcikova, K., & Michal, M. (2014). The leiomyomatous stroma in renal cell carcinomas is polyclonal and not part of the neoplastic process. Virchows archiv, 465(1), 89–96. 10.1007/s00428-014-1591-9
  84. Petersson, F., Sperga, M., Bulimbasic, S., Martinek, P., Svajdler, M., Kuroda, N., Hora, M., Simpson, R., Tichy, T., & Peckova, K. (2014). Foamy cell (hibernoma-like) change is a rare histopathological feature in renal cell carcinoma. Virchows Archiv, 465(2), 215–224. 10.1007/s00428-014-1600-z
  85. Vanecek, T., Halbhuber, Z., Kacerovska, D., Martinek, P., Sedivcova, M., Carr, R. A., Slouka, D., Michal, M., & Kazakov, D. V. (2014). Large germline deletions of the CYLD gene in patients with Brooke–Spiegler syndrome and multiple familial trichoepithelioma. The American Journal of Dermatopathology, 36(11), 868–874. 10.1097/dad.0000000000000068
  86. Grossmann, P., Vanecek, T., Steiner, P., Kacerovska, D., Spagnolo, D. V., Cribier, B., Rose, C., Vazmitel, M., Carlson, J. A., & Emberger, M. (2013). Novel and recurrent germline and somatic mutations in a cohort of 67 patients from 48 families with Brooke–Spiegler syndrome including the phenotypic variant of multiple familial trichoepitheliomas and correlation with the histopathologic findings in 379 biopsy specimens. The American Journal of Dermatopathology, 35(1), 34–44. 10.1097/dad.0b013e31824e7658
  87. Petersson, F., Grossmann, P., Hora, M., Sperga, M., Montiel, D. P., Martinek, P., Gutierrez, M. E. C., Bulimbasic, S., Michal, M., & Branzovsky, J. (2013). Renal cell carcinoma with areas mimicking renal angiomyoadenomatous tumor/clear cell papillary renal cell carcinoma. Human Pathology, 44(7), 1412–1420. 10.1016/j.humpath.2012.11.019
  88. Sperga, M., Martinek, P., Vanecek, T., Grossmann, P., Bauleth, K., Perez-Montiel, D., Alvarado-Cabrero, I., Nevidovska, K., Lietuvietis, V., & Hora, M. (2013). Chromophobe renal cell carcinoma—Chromosomal aberration variability and its relation to Paner grading system: An array CGH and FISH analysis of 37 cases. Virchows Archiv, 463(4), 563–573. 10.1007/s00428-013-1457-6
  89. Steiner, P., Hora, M., Stehlik, J., Martinek, P., Vanecek, T., Petersson, F., Michal, M., Korabecna, M., Travnicek, I., & Hes, O. (2013). Tubulocystic renal cell carcinoma: Is there a rational reason for targeted therapy using angiogenic inhibition? Analysis of seven cases. Virchows Archiv, 462(2), 183–192. 10.1007/s00428-012-1367-z
  90. Kacerovska, D., Cerna, K., Martinek, P., Grossmann, P., Michal, M., Ricar, J., & Kazakov, D. V. (2012). MSH6 mutation in a family affected by Muir–Torre syndrome. The American Journal of Dermatopathology, 34(6), 648–652. 10.1097/dad.0b013e3182446fe2
  91. Petersson, F., Bulimbasic, S., Hes, O., Slavik, P., Martínek, P., Michal, M., Gomolčáková, B., Hora, M., & Damjanov, I. (2012). Biphasic alveolosquamoid renal carcinoma: A histomorphological, immunohistochemical, molecular genetic, and ultrastructural study of a distinctive morphologic variant of renal cell carcinoma. Annals of diagnostic pathology, 16(6), 459–469. 10.1016/j.anndiagpath.2012.08.007

Kontakt

Email: martinek@biopticka.cz