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16 - Mesenchymal and Other Unusual Tumors of the Pleura and Peritoneum

Published online by Cambridge University Press:  16 March 2018

By
Nicole A. Cipriani  and
Peter Pytel
Edited by
Alberto M. Marchevsky ,
Aliya N. Husain  and
Françoise Galateau-Sallé
Alberto M. Marchevsky
Affiliation:
Cedars Sinai Medical Center, Los Angeles
Aliya N. Husain
Affiliation:
University of Chicago
Françoise Galateau-Sallé
Affiliation:
MESOPATH National Reference Center & Cancer Center Leon Berard
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Type
Chapter
Information
Practical Pathology of Serous Membranes , pp. 209 - 229
Publisher: Cambridge University Press
Print publication year: 2018

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References

Chung, EM, Biko, DM, Arzamendi, AM, Meldrum, JT, Stocker, JT. Solid tumors of the peritoneum, omentum, and mesentery in children: radiologic–pathologic correlation: from the radiologic pathology archives. RadioGraphics. 2015;35(2):521–46.CrossRefGoogle ScholarPubMed
Gladish, GW, Sabloff, BM, Munden, RF, Truong, MT, Erasmus, JJ, Chasen, MH. Primary thoracic sarcomas. RadioGraphics. 2002;22(3):621–37.CrossRefGoogle ScholarPubMed
Levy, AD, Arnaiz, J, Shaw, JC, Sobin, LH. From the archives of the AFIP: primary peritoneal tumors: imaging features with pathologic correlation. RadioGraphics. 2008;28(2):583–607, quiz 621–22.CrossRefGoogle ScholarPubMed
Vicens, RA, Patnana, M, Le, O, Bhosale, PR, Sagebiel, TL, Menias, CO, et al. Multimodality imaging of common and uncommon peritoneal diseases: a review for radiologists. Abdom Imaging. 2015;40(2):436–56.CrossRefGoogle ScholarPubMed
Joshi, A, McAndrew, N, Birdsall, S, Attanoos, RL. Clear cell sarcoma mimicking malignant pleural mesothelioma. Histopathology. 2008;53(3):359–61.CrossRefGoogle ScholarPubMed
Ju, HU, Seo, KW, Jegal, Y, Ahn, JJ, Lee, YJ, Kim, YM, et al. A case of alveolar soft part sarcoma of the pleura. J Korean Med Sci. 2013;28(2):331–35.CrossRefGoogle ScholarPubMed
Liang, W, Xu, S. Imaging findings from a case of pleural low-grade fibromyxoid sarcoma similar to mesothelioma with pleural effusion. Clin Respir J. 2016;10(1):120–24.CrossRefGoogle ScholarPubMed
Lee, CH, Park, CR, Kim, JW, Suh, JH, Lee, YJ, Jung, JP. Extraskeletal osteosarcoma arising from the pleura. Korean J Thorac Cardiovasc Surg. 2014;47(3):320–24.CrossRefGoogle ScholarPubMed
Cagle, PT, Allen, TC. Pathology of the pleura: what the pulmonologists need to know. Respirology. 2011;16(3):430–38.CrossRefGoogle ScholarPubMed
Marak, CP, Dorokhova, O, Guddati, AK. Solitary fibrous tumor of the pleura. Med Oncol. 2013;30(2):573.CrossRefGoogle ScholarPubMed
Cardillo, G, Lococo, F, Carleo, F, Martelli, M. Solitary fibrous tumors of the pleura. Curr Opin Pulm Med. 2012;18(4):339–46.CrossRefGoogle ScholarPubMed
Lee, KH, Song, KS, Kwon, Y, Lee, I, Lee, JS, Lim, TH. Mesenchymal tumours of the thorax: CT findings and pathological features. Clin Radiol. 2003;58(12):934–44.CrossRefGoogle ScholarPubMed
Vogels, RJ, Vlenterie, M, Versleijen-Jonkers, YM, Ruijter, E, Bekers, EM, Verdijk, MA, et al. Solitary fibrous tumor – clinicopathologic, immunohistochemical and molecular analysis of 28 cases. Diagn Pathol. 2014;9(1):224.CrossRefGoogle ScholarPubMed
Rao, N, Colby, TV, Falconieri, G, Cohen, H, Moran, CA, Suster, S. Intrapulmonary solitary fibrous tumors: clinicopathologic and immunohistochemical study of 24 cases. Am J Surg Pathol. 2013;37(2):155–66.CrossRefGoogle ScholarPubMed
Vallat-Decouvelaere, AV, Dry, SM, Fletcher, CD. Atypical and malignant solitary fibrous tumors in extrathoracic locations: evidence of their comparability to intra-thoracic tumors. Am J Surg Pathol. 1998;22(12):1501–11.CrossRefGoogle ScholarPubMed
England, DM, Hochholzer, L, McCarthy, MJ. Localized benign and malignant fibrous tumors of the pleura. A clinicopathologic review of 223 cases. Am J Surg Pathol. 1989;13(8):640–58.CrossRefGoogle ScholarPubMed
de Perrot, M, Fischer, S, Bründler, M-A, Sekine, Y, Keshavjee, S. Solitary fibrous tumors of the pleura. Ann Thorac Surg. 2002;74(1):285–93.CrossRefGoogle ScholarPubMed
Tapias, LF, Mercier, O, Ghigna, MR, Lahon, B, Lee, H, Mathisen, DJ, et al. Validation of a scoring system to predict recurrence of resected solitary fibrous tumors of the pleura. Chest. 2015;147(1):216–23.CrossRefGoogle ScholarPubMed
Schmid, S, Csanadi, A, Kaifi, JT, Kübler, M, Haager, B, Kayser, G, et al. Prognostic factors in solitary fibrous tumors of the pleura. J Surg Res. 2015;195(2):580–87.CrossRefGoogle ScholarPubMed
Mosquera, J-M, Fletcher, CDM. Expanding the spectrum of malignant progression in solitary fibrous tumors: a study of 8 cases with a discrete anaplastic component–is this dedifferentiated SFT? Am J Surg Pathol. 2009;33(9):1314–21.CrossRefGoogle ScholarPubMed
Doyle, LA, Vivero, M, Fletcher, CD, Mertens, F, Hornick, JL. Nuclear expression of STAT6 distinguishes solitary fibrous tumor from histologic mimics. Mod Pathol. 2014;27(3):390–95.CrossRefGoogle ScholarPubMed
Ng, TL, Gown, AM, Barry, TS, Cheang, MCU, Chan, AKW, Turbin, DA, et al. Nuclear beta-catenin in mesenchymal tumors. Mod Pathol. 2005;18(1):68–74.CrossRefGoogle ScholarPubMed
Langman, G, Rathinam, S, Papadaki, L. Primary localised pleural neurofibroma: expanding the spectrum of spindle cell tumours of the pleura. J Clin Pathol. 2010;63(2):116–18.CrossRefGoogle ScholarPubMed
Miguchi, M, Takakura, Y, Egi, H, Hinoi, T, Adachi, T, Kawaguchi, Y, et al. Malignant peripheral nerve sheath tumor arising from the greater omentum: case report. World J Surg Oncol. 2011;9:33.CrossRefGoogle ScholarPubMed
Boland, JM, Colby, TV, Folpe, AL. Intrathoracic peripheral nerve sheath tumors – a clinicopathological study of 75 cases. Hum Pathol. 2015;46(3):419–25.CrossRefGoogle ScholarPubMed
Antonescu, CR, Perry, A, Woodruff, JM. Schwannoma (including variants). In: Fletcher, CDM, Bridge, JA, Hogdendoorn, PCW, Mertens, F, Bosman, FT, Jaffe, ES, et al., editors. WHO classification of tumours of soft tissue and bone. Lyon: International Agency for Research on Cancer; 2013: 170–72.Google Scholar
Goldblum, JR, Folpe, AL, Weiss, SW. Enzinger and Weiss's soft tissue tumors. 6th edition. Philadelphia, PA: Elsevier; 2014.Google Scholar
Nascimento, AF, Fletcher, CD. The controversial nosology of benign nerve sheath tumors: neurofilament protein staining demonstrates intratumoral axons in many sporadic schwannomas. Am J Surg Pathol. 2007;31(9):1363–70.CrossRefGoogle ScholarPubMed
Wu, J, Zhu, H, Li, K, Yuan, CY, Wang, YF, Lu, GM. Imaging observations of pulmonary inflammatory myofibroblastic tumors in patients over 40 years old. Oncol Lett. 2015;9(4):1877–84.CrossRefGoogle ScholarPubMed
Coffin, CM, Hornick, JL, Fletcher, CDM. Inflammatory myofibroblastic tumor: comparison of clinicopathologic, histologic, and immunohistochemical features including ALK expression in atypical and aggressive cases. Am J Surg Pathol. 2007;31(4):509–20.CrossRefGoogle ScholarPubMed
Panagiotopoulos, N, Patrini, D, Gvinianidze, L, Woo, WL, Borg, E, Lawrence, D. Inflammatory myofibroblastic tumour of the lung: a reactive lesion or a true neoplasm? J Thorac Dis. 2015;7(5):908–11.Google ScholarPubMed
Siminovich, M, Galluzzo, L, López, J, Lubieniecki, F, de Dávila, MTG. Inflammatory myofibroblastic tumor of the lung in children: anaplastic lymphoma kinase (ALK) expression and clinico-pathological correlation. Pediatr Dev Pathol. 2012;15(3):179–86.CrossRefGoogle ScholarPubMed
Oguz, B, Ozcan, HN, Omay, B, Ozgen, B, Haliloglu, M. Imaging of childhood inflammatory myofibroblastic tumor. Pediatr Radiol. 2015;45(11):1672–81.CrossRefGoogle ScholarPubMed
Coffin, CM, Humphrey, PA, Dehner, LP. Extrapulmonary inflammatory myofibroblastic tumor: a clinical and pathological survey. Semin Diagn Pathol. 1998;15(2):85–101.Google ScholarPubMed
Coffin, CM, Watterson, J, Priest, JR, Dehner, LP. Extrapulmonary inflammatory myofibroblastic tumor (inflammatory pseudotumor). A clinicopathologic and immunohistochemical study of 84 cases. Am J Surg Pathol. 1995;19(8):859–72.CrossRefGoogle ScholarPubMed
Antonescu, CR, Suurmeijer, AJH, Zhang, L, Sung, YS, Jungbluth, AA, Travis, WD, et al. Molecular characterization of inflammatory myofibroblastic tumors with frequent ALK and ROS1 gene fusions and rare novel RET rearrangement. Am J Surg Pathol. 2015;39(7):957–67.CrossRefGoogle ScholarPubMed
Lovly, CM, Gupta, A, Lipson, D, Otto, G, Brennan, T, Chung, CT, et al. Inflammatory myofibroblastic tumors harbor multiple potentially actionable kinase fusions. Cancer Discov. 2014;4(8):889–95.CrossRefGoogle ScholarPubMed
Cook, JR, Dehner, LP, Collins, MH, Ma, Z, Morris, SW, Coffin, CM, et al. Anaplastic lymphoma kinase (ALK) expression in the inflammatory myofibroblastic tumor: a comparative immunohistochemical study. Am J Surg Pathol. 2001;25(11):1364–71.CrossRefGoogle ScholarPubMed
Hornick, JL, Sholl, LM, Dal, Cin P, Childress, MA, Lovly, CM. Expression of ROS1 predicts ROS1 gene rearrangement in inflammatory myofibroblastic tumors. Mod Pathol. 2015;28(5):732–39.CrossRefGoogle ScholarPubMed
Kovach, SJ, Fischer, AC, Katzman, PJ, Salloum, RM, Ettinghausen, SE, Madeb, R, et al. Inflammatory myofibroblastic tumors. J Surg Oncol. 2006;94(5):385–91.CrossRefGoogle ScholarPubMed
Tothova, Z, Wagner, AJ. Anaplastic lymphoma kinase-directed therapy in inflammatory myofibroblastic tumors. Curr Opin Oncol. 2012;24(4):409–13.CrossRefGoogle ScholarPubMed
Kasper, B, Baumgarten, C, Bonvalot, S, Haas, R, Haller, F, Hohenberger, P, et al. Management of sporadic desmoid-type fibromatosis: a European consensus approach based on patients “and professionals” expertise – a sarcoma patients EuroNet and European Organisation for Research and Treatment of Cancer/Soft Tissue and Bone Sarcoma Group initiative. Eur J Cancer. 2015;51(2):127–36.CrossRefGoogle ScholarPubMed
Otero, S, Moskovic, EC, Strauss, DC, Benson, C, Miah, AB, Thway, K, et al. Desmoid-type fibromatosis. Clin Radiol. 2015;70(9):1038–45.CrossRefGoogle ScholarPubMed
Fisher, C, Thway, K. Aggressive fibromatosis. Pathology. 2014;46(2):135–40.CrossRefGoogle ScholarPubMed
Carlson, JW, Fletcher, CDM, Fletcher, C. Immunohistochemistry for β-catenin in the differential diagnosis of spindle cell lesions: analysis of a series and review of the literature. Histopathology. 2007;51(4):509–14.CrossRefGoogle ScholarPubMed
Bhattacharya, B, Dilworth, HP, Iacobuzio-Donahue, C, Ricci, F, Weber, K, Furlong, MA, et al. Nuclear β-catenin expression distinguishes deep fibromatosis from other benign and malignant fibroblastic and myofibroblastic lesions. Am J Surg Pathol. 2005;29(5):653–59.CrossRefGoogle ScholarPubMed
Dei Tos, AP. Liposarcomas: diagnostic pitfalls and new insights. Histopathology. 2014;64(1):38–52.CrossRefGoogle ScholarPubMed
Okby, NT, Travis, WD. Liposarcoma of the pleural cavity: clinical and pathologic features of 4 cases with a review of the literature. Arch Pathol Lab Med. 2000;124(5):699–703.CrossRefGoogle ScholarPubMed
Wong, WW, Pluth, JR, Grado, GL, Schild, SE, Sanderson, DR. Liposarcoma of the pleura. Mayo Clin Proc. 1994;69(9):882–85.CrossRefGoogle ScholarPubMed
Grifasi, C, Calogero, A, Carlomagno, N, Campione, S, D'Armiento, FP, Renda, A. Intraperitoneal dedifferentiated liposarcoma showing MDM2 amplification: case report. World J Surg Oncol. 2013;11:305.CrossRefGoogle ScholarPubMed
Hasegawa, T, Seki, K, Hasegawa, F, Matsuno, Y, Shimodo, T, Hirose, T, et al. Dedifferentiated liposarcoma of retroperitoneum and mesentery: varied growth patterns and histological grades – a clinicopathologic study of 32 cases. Hum Pathol. 2000;31(6):717–27.CrossRefGoogle ScholarPubMed
Chen, M, Yang, J, Zhu, L, Zhou, C, Zhao, H. Primary intrathoracic liposarcoma: a clinicopathologic study and prognostic analysis of 23 cases. J Cardiothorac Surg. 2014;9:119.CrossRefGoogle ScholarPubMed
Zidane, A, Atoini, F, Arsalane, A, Traibi, A, Hammoumi, M, Ouariachi, F, et al. Parietal pleura lipoma: a rare intrathoracic tumor. Gen Thorac Cardiovasc Surg. 2011;59(5):363–66.CrossRefGoogle ScholarPubMed
Sakurai, H, Kaji, M, Yamazaki, K, Suemasu, K. Intrathoracic lipomas: their clinicopathological behaviors are not as straightforward as expected. Ann Thorac Surg. 2008;86(1):261–65.CrossRefGoogle Scholar
Evans, HL. Atypical lipomatous tumor, its variants, and its combined forms: a study of 61 cases, with a minimum follow-up of 10 years. Am J Surg Pathol. 2007;31(1):1–14.CrossRefGoogle ScholarPubMed
Thway, K, Flora, R, Shah, C, Olmos, D, Fisher, C. Diagnostic utility of p16, CDK4, and MDM2 as an immunohistochemical panel in distinguishing well-differentiated and dedifferentiated liposarcomas from other adipocytic tumors. Am J Surg Pathol. 2012;36(3):462–69.CrossRefGoogle ScholarPubMed
Tavassoli, FA, Norris, HJ. Peritoneal leiomyomatosis (leiomyomatosis peritonealis disseminata): a clinicopathologic study of 20 cases with ultrastructural observations. Int J Gynecol Pathol. 1982;1(1):59–74.CrossRefGoogle ScholarPubMed
Al-Talib, A, Tulandi, T. Pathophysiology and possible iatrogenic cause of leiomyomatosis peritonealis disseminata. Gynecol Obstet Invest. 2010;69(4):239–44.CrossRefGoogle ScholarPubMed
Parmley, TH, Woodruff, JD, Winn, K, Johnson, JW, Douglas, PH. Histogenesis of leiomyomatosis peritonealis disseminata (disseminated fibrosing deciduosis). Obstet Gynecol. 1975;46(5):511–16.Google ScholarPubMed
Düe, W, Pickartz, H. Immunohistologic detection of estrogen and progesterone receptors in disseminated peritoneal leiomyomatosis. Int J Gynecol Pathol. 1989;8(1):46–53.CrossRefGoogle ScholarPubMed
Bekkers, RL, Willemsen, WN, Schijf, CP, Massuger, LF, Bulten, J, Merkus, JM. Leiomyomatosis peritonealis disseminata: does malignant transformation occur? A literature review. Gynecologic Oncology. 1999;75(1):158–63.CrossRefGoogle ScholarPubMed
Lin, BT, Colby, T, Gown, AM, Hammar, SP, Mertens, RB, Churg, A, et al. Malignant vascular tumors of the serous membranes mimicking mesothelioma. A report of 14 cases. Am J Surg Pathol. 1996;20(12):1431–39.CrossRefGoogle ScholarPubMed
Anderson, T, Zhang, L, Hameed, M, Rusch, V, Travis, WD, Antonescu, CR. Thoracic epithelioid malignant vascular tumors: a clinicopathologic study of 52 cases with emphasis on pathologic grading and molecular studies of WWTR1–CAMTA1 fusions. Am J Surg Pathol. 2015;39(1):132–39.CrossRefGoogle ScholarPubMed
Suzuki, F, Saito, A, Ishi, K, Koyatsu, J, Maruyama, T, Suda, K. Intra-abdominal angiosarcomatosis after radiotherapy. J Gastroenterol Hepatol. 1999;14(3):289–92.CrossRefGoogle ScholarPubMed
Suster, S, Moran, CA, Koss, MN. Epithelioid hemangioendothelioma of the anterior mediastinum. Clinicopathologic, immunohistochemical, and ultrastructural analysis of 12 cases. Am J Surg Pathol. 1994;18(9):871–81.CrossRefGoogle ScholarPubMed
Khong, PL, Chan, GC, Shek, TW, Tam, PK, Chan, FL. Imaging of peripheral PNET: common and uncommon locations. Clin Radiol. 2002;57(4):272–77.CrossRefGoogle ScholarPubMed
Tanida, S, Tanioka, F, Inukai, M, Yoshioka, N, Saida, Y, Imai, K, et al. Ewing's sarcoma/peripheral primitive neuroectodermal tumor (pPNET) arising in the omentum as a multilocular cyst with intracystic hemorrhage. J Gastroenterol. 2000;35(12):933–40.CrossRefGoogle ScholarPubMed
Askin, FB, Rosai, J, Sibley, RK, Dehner, LP, McAlister, WH. Malignant small cell tumor of the thoracopulmonary region in childhood: a distinctive clinicopathologic entity of uncertain histogenesis. Cancer. 1979;43(6):2438–51.3.0.CO;2-9>CrossRefGoogle ScholarPubMed
Angervall, L, Enzinger, FM. Extraskeletal neoplasm resembling Ewing's sarcoma. Cancer. 1975;36(1):240–51.3.0.CO;2-H>CrossRefGoogle ScholarPubMed
Aurias, A, Rimbaut, C, Buffe, D, Zucker, JM, Mazabraud, A. Translocation involving chromosome 22 in Ewing's sarcoma. A cytogenetic study of four fresh tumors. Cancer Genet Cytogenet. 1984;12(1):21–25.CrossRefGoogle ScholarPubMed
Whang-Peng, J, Triche, TJ, Knutsen, T, Miser, J, Douglass, EC, Israel, MA. Chromosome translocation in peripheral neuroepithelioma. N Engl J Med. 1984;311(9):584–85.CrossRefGoogle ScholarPubMed
Folpe, AL, Goldblum, JR, Rubin, BP, Shehata, BM, Liu, W, Dei Tos, AP, et al. Morphologic and immunophenotypic diversity in Ewing family tumors: a study of 66 genetically confirmed cases. Am J Surg Pathol. 2005;29(8):1025–33.CrossRefGoogle ScholarPubMed
Tsokos, M, Alaggio, RD, Dehner, LP, Dickman, PS. Ewing sarcoma/peripheral primitive neuroectodermal tumor and related tumors. Pediatr Dev Pathol. 2012;15(1 Suppl):108–26.CrossRefGoogle ScholarPubMed
Subbiah, V, Anderson, P, Lazar, AJ, Burdett, E, Raymond, K, Ludwig, JA. Ewing's sarcoma: standard and experimental treatment options. Curr Treat Options Oncol. 2009;10(1–2):126–40.CrossRefGoogle ScholarPubMed
Prat, J, Matias-Guiu, X, Algaba, F. Desmoplastic small round-cell tumor. Am J Surg Pathol. 1992;16(3):306–07.CrossRefGoogle ScholarPubMed
Karavitakis, EM, Moschovi, M, Stefanaki, K, Karamolegou, K, Dimitriadis, E, Pandis, N, et al. Desmoplastic small round cell tumor of the pleura. Pediatr Blood Cancer. 2007;49(3):335–38.CrossRefGoogle ScholarPubMed
Antonescu, CR, Ladanyi, M. Desmoplastic small round cell tumour. In: Fletcher, CDM, Bridge, JA, Hogdendoorn, PCW, Mertens, F, Bosman, FT, Jaffe, ES, et al., editors. WHO classification of tumours of soft tissue and bone. Lyon: International Agency for Research on Cancer; 2013: 225–27.Google Scholar
Messinger, YH, Stewart, DR, Priest, JR, Williams, GM, Harris, AK, Schultz, KA, et al. Pleuropulmonary blastoma: a report on 350 central pathology-confirmed pleuropulmonary blastoma cases by the International Pleuropulmonary Blastoma Registry. Cancer. 2015;121(2):276–85.CrossRefGoogle ScholarPubMed
Doros, L, Schultz, KA, Stewart, DR, Bauer, AJ, Williams, G, Rossi, CT, et al. DICER1-related disorders. In: Pagon, RA, Adam, MP, Ardinger, HH, Wallace, SE, Amemiya, A, Bean, LJH, et al., editors. GeneReviews(R). Seattle, WA; 1993.Google Scholar
Hachitanda, Y, Aoyama, C, Sato, JK, Shimada, H. Pleuropulmonary blastoma in childhood. A tumor of divergent differentiation. Am J Surg Pathol. 1993;17(4):382–91.CrossRefGoogle ScholarPubMed
Manivel, JC, Priest, JR, Watterson, J, Steiner, M, Woods, WG, Wick, MR, et al. Pleuropulmonary blastoma. The so-called pulmonary blastoma of childhood. Cancer. 1988;62(8):1516–26.3.0.CO;2-3>CrossRefGoogle ScholarPubMed
de Krijger, RR, Claessen, SM, van der Ham, F, van Unnik, AJ, Hulsbergen-van de Kaa, CA, van Leuven, L, et al. Gain of chromosome 8q is a frequent finding in pleuropulmonary blastoma. Mod Pathol. 2007;20(11):1191–99.CrossRefGoogle ScholarPubMed
Pugh, TJ, Yu, W, Yang, J, Field, AL, Ambrogio, L, Carter, SL, et al. Exome sequencing of pleuropulmonary blastoma reveals frequent biallelic loss of TP53 and two hits in DICER1 resulting in retention of 5p-derived miRNA hairpin loop sequences. Oncogene. 2014;33(45):5295–302.CrossRefGoogle ScholarPubMed
Kim, GH, Kim, MY, Koo, HJ, Song, JS, Choi, C-M. Primary pulmonary synovial sarcoma in a tertiary referral center: clinical characteristics, CT, and 18F-FDG PET findings, with pathologic correlations. Medicine (Baltimore). 2015;94(34):e1392.CrossRefGoogle Scholar
Goldblatt, J, Saxena, P, McGiffin, DC, Zimmet, A. Pericardial synovial sarcoma: a rare clinical entity. J Card Surg. 2015;30(11):801–04.CrossRefGoogle ScholarPubMed
Hemmings, C, Fisher, C. Primary omental synovial sarcoma: a case with cytogenetic confirmation. Pathology. 2004;36(2):208–11.CrossRefGoogle ScholarPubMed
Mirzoyan, M, Muslimani, A, Setrakian, S, Swedeh, M, Daw, HA. Primary pleuropulmonary synovial sarcoma. Clin Lung Cancer. 2008;9(5):257–61.CrossRefGoogle ScholarPubMed
van de Rijn, M, Barr, FG, Xiong, QB, Hedges, M, Shipley, J, Fisher, C. Poorly differentiated synovial sarcoma: an analysis of clinical, pathologic, and molecular genetic features. Am J Surg Pathol. 1999;23(1):106–12.CrossRefGoogle ScholarPubMed
Foo, WC, Cruise, MW, Wick, MR, Hornick, JL. Immunohistochemical staining for TLE1 distinguishes synovial sarcoma from histologic mimics. Am J Clin Pathol. 2011;135(6):839–44.CrossRefGoogle ScholarPubMed
Kosemehmetoglu, K, Vrana, JA, Folpe, AL. TLE1 expression is not specific for synovial sarcoma: a whole section study of 163 soft tissue and bone neoplasms. Mod Pathol. 2009;22(7):872–78.CrossRefGoogle Scholar

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