View Item 

Show simple item record

Cytologic and histological features of rare nonepithelial and nonlymphoid tumors of the thyroid
dc.contributor.authorRossi, Esther Diana
dc.contributor.authorPantanowitz, Liron
dc.contributor.authorHornick, Jason L.
dc.date.accessioned2021-09-08T14:37:02Z
dc.date.available2022-09-08 10:37:00en
dc.date.available2021-09-08T14:37:02Z
dc.date.issued2021-08
dc.identifier.citationRossi, Esther Diana; Pantanowitz, Liron; Hornick, Jason L. (2021). "Cytologic and histological features of rare nonepithelial and nonlymphoid tumors of the thyroid." Cancer Cytopathology (8): 583-602.
dc.identifier.issn1934-662X
dc.identifier.issn1934-6638
dc.identifier.urihttps://hdl.handle.net/2027.42/169326
dc.publisherWolters Kluwer
dc.publisherWiley Periodicals, Inc.
dc.subject.otherthyroid nodules
dc.subject.otherfine needle aspiration cytology
dc.subject.othermalignancy
dc.subject.othernonepithelial tumors
dc.subject.otherrare thyroid entities
dc.subject.othersarcoma
dc.titleCytologic and histological features of rare nonepithelial and nonlymphoid tumors of the thyroid
dc.typeArticle
dc.rights.robotsIndexNoFollow
dc.subject.hlbsecondlevelOncology and Hematology
dc.subject.hlbtoplevelHealth Sciences
dc.description.peerreviewedPeer Reviewed
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/169326/1/cncy22404_am.pdf
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/169326/2/cncy22404.pdf
dc.identifier.doi10.1002/cncy.22404
dc.identifier.sourceCancer Cytopathology
dc.identifier.citedreferenceLayfield LJ, Kakudo K. Metastatic tumors, lymphoma and rare tumors of the thyroid. In: Ali S, Cibas ES, eds. The Bethesda System for Reporting Thyroid Cytopathology. 2 nd ed. Springer; 2018: 218 ‐ 221.
dc.identifier.citedreferenceWu X, Chen S, Zhang LY, et al. Langerhans cell histiocytosis of the thyroid complicated by papillary thyroid carcinoma. A case report and brief literature review. Medicine (Baltimore). 2017; 96: e7954.
dc.identifier.citedreferenceKuhn E, Ragazzi M, Zini M, et al. Critical pitfalls in the use of BRAF mutation as a diagnostic tool in thyroid nodules: a case report. Endocr Pathol. 2016; 27: 220 ‐ 223.
dc.identifier.citedreferenceMoschovi M, Adamaki M, Vlahopoulos S, Rodriguez‐Galindo C. Synchronous and metachronous thyroid cancer in relation to Langerhans cell histiocytosis: involvement of V600E BRAF‐mutation? Pediatr Blood Cancer. 2015; 62: 173 ‐ 174.
dc.identifier.citedreferencePhulware RH, Guleria P, Iyer VK, et al. Cytological diagnosis of Langerhans cell histiocytosis: a series of 47 cases. Cytopathol. 2019; 30: 413 ‐ 418.
dc.identifier.citedreferenceHang JF, Siddiqui MT, Ali SZ. Fine needle aspiration of Langerhans cell histiocytosis: a cytopathologic study of 37 cases. Acta Cytol. 2017; 61: 96 ‐ 102.
dc.identifier.citedreferenceAl Hamad M, Albisher HM, Al Saeed WR, et al. BRAF gene mutations in synchronous papillary thyroid carcinoma and Langerhans cell histiocytosis co‐existing in the thyroid gland: a case report and literature review. BMC Cancer. 2019; 19: 170.
dc.identifier.citedreferenceGuarino S, Giusti DM, Rubini A, et al. Association between pituitary Langerhans cell histiocytosis and papillary thyroid carcinoma. Clin Med Insights Case Rep. 2013; 9: 197 ‐ 200.
dc.identifier.citedreferenceVujhini SK, Kolte SS, Satarkar RN, Srikanth S. Fine needle aspiration diagnosis of Rosai‐Dorfman disease involving thyroid. J Cytol. 2012; 29: 83 ‐ 85.
dc.identifier.citedreferenceGianella P, Dulguerov N, Arnoux G, Pusztaszeri M, Seebach JD. Thyroid Rosai‐Dorfman disease with infiltration of IgG4‐bearing plasma cells associated with multiple small pulmonary cysts. BMC Pulmonary Medicine. 2019; 19: 83 ‐ 87.
dc.identifier.citedreferenceEmile JF, Abla O, Fraitag S, et al. Histiocyte society. Revised classification of histiocytoses and neoplasms of the machropage‐dendritic cell lineage. Blood. 2016; 127: 2672 ‐ 2681.
dc.identifier.citedreferenceRosai J, Dorfman RF. Sinus histiocytosis with massive lymphadenopathy. A newly recognized benign clinicopathological entity. Arch Pathol. 1969; 87: 63 ‐ 70.
dc.identifier.citedreferenceFoucar E, Rosai J, Dorfman RF. Sinus histiocytosis with massive lymphadenopathy (Rosai‐Dorfman disease): review of the entity. Semin Diagn Pathol. 1990; 7: 19 ‐ 73.
dc.identifier.citedreferenceLee FY, Jan YJ, Chou G, Wang J, Wang CC. Thyroid involvement in Rosai‐Dorfman disease. Thyroid. 2007; 17: 471 ‐ 476.
dc.identifier.citedreferencePalmas Candia F, Porras Ledantes JA, Raventós Estellé A, Simón Muela I, Vendrell Ortega J, Näf Cortés S. Thyroid involvement by Rosai‐Dorfman disease. Endocrinol Diabetes Nutr. 2017; 64: 280 ‐ 281.
dc.identifier.citedreferencePowell GJ, Goellner JR, Nowak LE, McIver B. Rosai‐Dorfman disease of the thyroid masquerading as anaplastic carcinoma. Thyroid. 2003; 13: 217 ‐ 221.
dc.identifier.citedreferenceOak CY, Kim HK, Yoon TM, et al. Benign teratoma of the thyroid gland. Endocrinol Metab. 2013; 28: 144 ‐ 148.
dc.identifier.citedreferenceRiedlinger WF, Lack EE, Robson CD, Rahbar R, Nosé V. Primary thyroid teratomas in children: a report of 11 cases with a proposal of criteria for their diagnosis. Am J Surg Pathol. 2005; 29: 700 ‐ 706.
dc.identifier.citedreferenceThompson LDR, Rosai J, Heffess CS. Primary thyroid teratomas: a clinicopathologic study of 30 cases. Cancer. 2000; 88: 1149 ‐ 1158.
dc.identifier.citedreferenceJayaram G, Cheah PL, Yip CH. Malignant teratoma of the thyroid with predominantly neuroepithelial differentiation: fine needle aspiration cytologic, histologic and immunocytochemical features of a case. Acta Cytol. 2000; 44: 375 ‐ 379.
dc.identifier.citedreferenceMartins T, Carriho F, Gomes L, et al. Malignant teratoma of the thyroid gland: case report. Thyroid. 2006; 16: 1311 ‐ 1313.
dc.identifier.citedreferenceStarling CE, Sabra J, Brady B, Horton M, Traweek ST. Malignant teratoma of the thyroid. A difficult diagnosis by fine‐needle aspiration. Diagn Cytopathol. 2019; 47: 930 ‐ 934.
dc.identifier.citedreferenceCibas ES, Ali SZ (eds). Medullary thryoid carcinoma. In: The 2017 Bethesda System for Reporting Thyroid Cytopathology. Springer International; 2017: 157 ‐ 175.
dc.identifier.citedreferenceCan AS, Koksal G. Thyroid metastasis from small cell lung carcinoma: a case report and review of the literature. J Med Case Rep. 2015; 9: 231.
dc.identifier.citedreferenceOzaki O, Sugino K, Mimura T, et al. Primary leiomyosarcoma of the thyroid gland. Surg Today. 1997; 27: 177 ‐ 180.
dc.identifier.citedreferenceThompson LDR. Rare primary thyroid nonepithelial tumors and tumor‐like conditions. In: Nikiforov YE, Biddinger PW, Thompson LDR, eds. Diagnostic Pathology and Molecular Genetics of the Thyroid. 3 rd ed. Wolters Kluwer; 2020: 419 ‐ 452.
dc.identifier.citedreferenceWick MR, Eusebi V, Lamovec J, et al. Tumors of the thyroid gland. In: Lloyd RV, Osamura RY, Kloppel G, et al, eds. World Health Organization Classification of Tumors of Endocrine Organs. IARC; 2017: 52 ‐ 62.
dc.identifier.citedreferenceSurov A, Gottschling S, Wienke A, et al. Primary thyroid sarcoma: a systematic review. Anticancer Res. 2015; 35: 5185 ‐ 5191.
dc.identifier.citedreferenceBaloch ZW, LiVolsi VA. Unusual tumors of the thyroid gland. Endocrinol Metab Clin North Am. 2008; 37: 297 ‐ 310.
dc.identifier.citedreferenceGeller RL, Hookim K, Sullivan HC, et al. Cytologic features of angiosarcoma: a review of 26 cases diagnosed on FNA. Cancer Cytopathol. 2016; 124: 659 ‐ 668.
dc.identifier.citedreferenceIto YK, Nakashima T, Mori T. Pathomorphologic characteristics of 102 cases of thorotrast‐related hepatocellular carcinoma, cholangiocarcinoma and hepatic angiosarcoma. Cancer. 1988; 62: 1153 ‐ 1162.
dc.identifier.citedreferenceFalk S, Krishnan J, Meis JM. Primar angiosarcoma of the spleen. A clinicopathologic study of 40 cases. Am J Surg Pathol. 1993; 17: 959 ‐ 970.
dc.identifier.citedreferenceRandall MB, Geisinger KR. Angiosarcoma of the heart: pericardial fluid cytology. Diagn Cytopathol. 1990; 6: 58 ‐ 62.
dc.identifier.citedreferenceLin O, Gerhard R, Coelho Siqueira SA, De Castro IV. Cytological findings of epithelioid angiosarcoma of the thyroid. A case report. Acta Cytol. 2002; 46: 767 ‐ 771.
dc.identifier.citedreferenceHasegawa T, Fujii Y, Seki K, et al. Epithelioid angiosarcoma of the bone. Hum Pathol. 1997; 28: 985 ‐ 989.
dc.identifier.citedreferenceKuhn E, Ragazzi M, Ciarrocchi A, et al. Angiosarcoma and anaplastic carcinoma of the thyroid are two distinct entities: a morphologic, immunohistochemical, and genetic study. Mod Pathol. 2019; 32: 787 ‐ 798.
dc.identifier.citedreferenceBoucher LD, Swanson PE, Stanley MW, et al. Cytology of angiosarcoma. Findings in fourteen fine‐needle aspiration biopsy specimen and one pleural fluid specimen. Am J Clin Pathol. 2000; 114: 210 ‐ 219.
dc.identifier.citedreferenceLiu K, Layfield LJ. Cytomorphologic features of angiosarcoma on fine needle aspiration biopsy. Acta Cytol. 1999; 43: 407 ‐ 415.
dc.identifier.citedreferenceMinimo C, Zakowski M, Lin O. Cytologic findings of malignant vascular neoplasms: a study of twenty‐four cases. Diagn Cytopathol. 2002; 26: 349 ‐ 355.
dc.identifier.citedreferenceMiao J, Chen S, Li Y, Fu L, Lia H. Primary cavernous hemangioma of the thyroid gland: a case report and literature review. Medicine (Baltimore). 2017; 96: e8651.
dc.identifier.citedreferenceRice CO. Hemangioendothelioma of thyroid gland. Am J Cancer. 1931; 15: 2301 ‐ 2308.
dc.identifier.citedreferenceChen KT, Kinkegaard DD, Bocian JJ. Angiosarcoma of the breast. Cancer. 1980; 46: 368 ‐ 371.
dc.identifier.citedreferenceWick MR, Eusebi V, Lamovec J, Ryska A. Angiosarcoma. In: Lloyd RV, Osamura RY, Klöppel G, Rosai J, eds. WHO Classification of Tumors of Endocrine Organs. 4 th ed. Volume 10. IARC: 2017: 129 ‐ 132.
dc.identifier.citedreferenceVanderbussche CJ, Wakely PE, Siddiqui MT, Maleki Z, Ali SZ. Cytopathologic characteristics of epithelioid vascular malignancies. Acta Cytol. 2014; 58: 356 ‐ 366.
dc.identifier.citedreferenceThompson LD, Wenig BM, Adair CF, Heffess CS. Peripehral nerve sheath tumors of the thyroid gland. A series of four cases and a review of the literature. Endocr Pathol. 1996; 7: 309 ‐ 318.
dc.identifier.citedreferenceNagavalli S, Yehuda M, McPhaul LW, et al. A cervical schwannoma masquerading as a thyroid nodule. Eur Thyroid J. 2017; 6: 216 ‐ 220.
dc.identifier.citedreferenceChen G, Liu Z, Su C, et al. Primary peripheral nerve sheath tumors of the thyroid gland: a case report and literature review. Mol Clin Oncol. 2016; 4: 209 ‐ 210.
dc.identifier.citedreferenceCapelli A, Guernelli L, Bertoni F, Fuga G. Neurofibroma of the thyroid gland (report of a case). Arch Chir Torac Cardiovasc. 1975; 32: 23 ‐ 27.
dc.identifier.citedreferenceGaud U, Shukla K, Kumar M, Pandey M. Isolated intrathyroidal neurofibroma. Otolaryngol Head Neck Surg. 2009; 141: 300 ‐ 301.
dc.identifier.citedreferenceKandil E, Khalek MB, Abdullah O, et al. Primary peripheral nerve sheath tumors of the thyroid gland. Thyroid. 2010; 20: 583 ‐ 586.
dc.identifier.citedreferenceJayaram G. Neurilemmoma (schwannoma) of the thyroid diagnosed by fine needle aspiration cytology. Acta Cytol. 1999; 43: 743 ‐ 744.
dc.identifier.citedreferenceBaglaj M, Markowska‐Woyciechowska A, Sawicz‐Birkowska K, et al. Primary neurilemmoma of the thyroid gland in a 12‐year‐old girl. J Pediatr Surg. 2004; 38: 1418 ‐ 1420.
dc.identifier.citedreferenceYu GH, Sack MJ, Baloch Z, et al. Difficulties in the fine needle aspiration (FNA) diagnosis of schwannoma. Cytopathology. 1999; 10: 186 ‐ 194.
dc.identifier.citedreferenceZheng X, Guo K, Wang H, et al. Extracranial schwannoma in the carotid space: a retrospective review of 91 cases. Head Neck. 2017; 39: 42 ‐ 47.
dc.identifier.citedreferenceKasraeian S, Allison DC, Ahlmann ER, et al. A comparison of fine‐needle aspiration, core biopsy, and surgical biopsy in the diagnosis of extremity soft tissue masses. Clin Orthop Relat Res. 2010; 468: 2992 ‐ 3002.
dc.identifier.citedreferenceAhn D, Lee GJ, Sohn JH, et al. Fine‐needle aspiration cytology versus core‐needle biopsy for the diagnosis of extracranial head and neck schwannoma. Head Neck. 2018; 40: 2695 ‐ 2700.
dc.identifier.citedreferenceKang JY, Yi KS, Cha SH, et al. Schwannoma of the thyroid bed. A case report and review of literature. Medicine (Baltimore). 2020; 99: e18814.
dc.identifier.citedreferenceWakely PE, Ali SZ, Bishop J. The cytopathology of malignant peripheral nerve sheath tumor. A report of 55 fine‐needle aspiration cases. Cancer Cytopathol. 2012; 120: 334 ‐ 341.
dc.identifier.citedreferenceSchaefer IM, Fletcher C, Hornick JL. Loss of H3K27 trimethylation distinguishes malignant peripheral nerve sheath tumors from histologic mimics. Mod Pathol. 2016; 29: 4 ‐ 13.
dc.identifier.citedreferenceMiller DL, Thompson LDR, Bishop JA, Rooper LM, Ali SZ. Malignant teratomas of the thyroid gland: clinico‐radiologic and cytomorphologic features of a rare entity. J Am Soc Cytopathol. 2020; 9: 221 ‐ 231.
dc.identifier.citedreferenceMito JK, Qian X, Doyle LA, Hornick JL, Jo V. Role of histone H3K27 trimethylation loss as a marker for malignant peripheral nerve sheath tumor in fine‐needle aspiration and small biopsy specimens. Am J Clin Pathol. 2017; 148: 179 ‐ 189.
dc.identifier.citedreferenceCetin S, Kir G, Yilmaz M. Thyroid paraganglioma diagnosed by fine needle aspiration biopsy, correlated with histopathological findings. Report of a case. Diagn Cytopathol. 2016; 44: 643 ‐ 647.
dc.identifier.citedreferenceKiriakopoulos A, Linos D. Thyroid paraganglioma: a case report of a rare head and neck tumor. J Surg Case Rep. 2018; 8: 1 ‐ 3.
dc.identifier.citedreferenceLack EE, Cubila AL, Woodruff JM. Paragangliomas of the head and neck region. A pathologic study of tumors from 71 parents. Hum Pathol. 1979; 10: 191 ‐ 218.
dc.identifier.citedreferenceBaloch ZW, LiVolsi VA. Neuroendocrine tumors of the thyroid gland. Am J Clin Pathol. 2002; 115: 556 ‐ 567.
dc.identifier.citedreferenceDe Tullio A, Lisco G, Duda L, Renzulli G, Triggiani V. Medullary thyroid cancer with paraganglioma‐like pattern diagnosed during pregnancy: a case report and literature revision. Endocr Metab Immune Disord Drug Targets. 2020; 20: 295 ‐ 302.
dc.identifier.citedreferenceZhang W, Policarpio‐Nicolas MLC. Aspiration cytology of primary thyroid paraganglioma. Diagn Cytopathol. 2015; 43: 838 ‐ 843.
dc.identifier.citedreferenceLaGuette J, Matias‐Guiu X, Rosai J. Thyroid paraganglioma: a clinicopathologic and immunohistochemical study of three cases. Am J Surg Pathol. 1997; 21: 748 ‐ 752.
dc.identifier.citedreferencePlaza JA, Wakely PE Jr, Moran C, Fletcher CD, Suster S. Sclerosing paraganglioma: report of 19 cases of an unusual variant of neuroendocrine tumor that may be mistaken for an aggressive malignant neoplasm. Am J Surg Pathol. 2006; 30: 7 ‐ 11.
dc.identifier.citedreferenceVon Dobschuetz E, Leijon H, Schalin‐Jantti C, et al. A registry‐based study of thyroid paraganglioma: histological and genetics characteristics. Endocr Relat Cancer. 2015; 22: 191 ‐ 204.
dc.identifier.citedreferenceJohnson TL, Zarbo RJ, Lloyd RV, Crissman JD. Paragangliomas of the head and neck: immunohistochemical neuroendocrine and intermediate filament typing. Mod Pathol. 1988; 1: 216 ‐ 223.
dc.identifier.citedreferenceSatturwar S, Rossi ED, Maleki Z, Canton R, Faquin W, Pantanowitz L. Thyroid paraganglioma: a diagnostic pitfall in thyroid FNA. Cancer Cytopathology. Published online November 24, 2020. doi: 10.1002/cncy.22390
dc.identifier.citedreferenceCostinean S, Balatti V, Bottoni A, et al. Primary intrathyroidal paraganglioma: histopathology and novel molecular alterations. Human Pathol. 2012; 43: 2371 ‐ 2375.
dc.identifier.citedreferenceZantour B, Guilhaume B, Tissier F, et al. A thyroid nodule revealing a paraganglioma in a patient with a new germline mutation in the succinate dehydrogenase B gene. Eur J Endocrinol. 2004; 151: 433 ‐ 438.
dc.identifier.citedreferenceKaushal S, Iyer VK, Mathur SR, Ray R. Fine needle aspiration cytology of medullary carcinoma of the thyroid with a focus on rare variants: a review of 78 cases. Cytopathol. 2011; 22: 95 ‐ 106.
dc.identifier.citedreferenceMilias S, Hytiroglou P, Kourtis D, et al. Granular cell tumor of the thyroid gland. Histopathology. 2004; 44: 190 ‐ 191.
dc.identifier.citedreferenceAbrikossoff A. Uber myome ausgehend von der quergestreiften willkurlichen muskulatur. Virchows Arch Pathol Anat. 1926; 260: 215 ‐ 233.
dc.identifier.citedreferenceFiner EB, Villalba JA, Pitman MB, et al. Granular cell tumor of the lung. Diagn Cytopathol. 2019; 47: 345 ‐ 346.
dc.identifier.citedreferenceCorso G, Di Nubila B, Ciccia A, et al. Granular cell tumor of the breast: molecular pathology and clinical management. Breast J. 2018; 24: 778 ‐ 782.
dc.identifier.citedreferenceUlivieri S, Muscas G, Lavalle L, et al. Granular cell tumor of the orbit: pathological features and treatment. J Neurosurg Sci. 2017; 61: 342 ‐ 343.
dc.identifier.citedreferenceDomínguez‐González M, Nogales‐Pérez A, Vázquez Navarrete S, et al. Granular cell tumor of the vulva. J Low Genit Tract Dis. 2013; 17: 82 ‐ 84.
dc.identifier.citedreferenceAlmaghrabi M, Almaghrabi H, Al‐Magrhabi H. Granular cell tumor of thyroid: challenging pitfalls and mimickers in diagnosis. J Microsc Ultrastruct. 2020; 8: 1 ‐ 6.
dc.identifier.citedreferenceBowry M, Almeida B, Jeannon JP. Granular cell tumour of the thyroid gland: a case report and review of the literature. Endocr Pathol. 2011; 22: 1 ‐ 5.
dc.identifier.citedreferenceXu D, Zhuang S, Liao S, Lv Y, Yu J. Granular cell tumor of the thyroid in a 16‐year‐old girl: a rare entity. Int J Clin Exp Pathol. 2016; 9: 1499 ‐ 1503.
dc.identifier.citedreferenceDu ZH, Qiu HY, Wei T, Zhu JQ. Granular cell tumor of the thyroid: clinical and pathological characteristics of a rare case in a 14‐year‐old girl. Oncol Lett. 2015; 9: 777 ‐ 779.
dc.identifier.citedreferencePark WC, Choi SH, Lee YS. Granular cell tumor of the thyroid gland: a case report and review of the literature. Korean J Endocr Surg. 2015; 15: 20 ‐ 24.
dc.identifier.citedreferenceChen Q, Li Q, Guo L, Li S, Jiang Y. Fine needle aspiration cytology of a granular cell tumor arising in the thyroid gland: a case report and review of literature. Int J Clin Exp Pathol. 2014; 7: 5186 ‐ 5191.
dc.identifier.citedreferenceHarp E, Caraway NP. FNA of thyroid granular cell tumor. Diagn Cytopathol. 2013; 41: 825 ‐ 828.
dc.identifier.citedreferenceMin KW, Paik SS, Jun YJ, Han H, Jang KS. Fine needle aspiration cytology of a granular cell tumour arising in the thyroid gland. Cytopathology. 2012; 23: 411 ‐ 412.
dc.identifier.citedreferenceSingh S, Gupta N, Sharma S, Azad RK. Aspiration cytology in the preoperative diagnosis of granular cell tumor of thyroid region in an 11‐years‐old female child. J Cytol. 2013; 30: 218 ‐ 219.
dc.identifier.citedreferenceKlemperer P, Rabin CB. Primary neoplasms of the pleura: a report of five cases. Arch Pathol. 1931; 11: 385 ‐ 412.
dc.identifier.citedreferencePapi G, Corradi S, LiVolsi VA. Primary spindle cell lesions of the thyroid gland. An overview. Am J Clin Pathol. 2006; 125 ( suppl ): S95 ‐ S123.
dc.identifier.citedreferenceDeng XR, Wang G, Kuang CJ, et al. Metastasis of leiomyosarcoma of the thyroid. Clin Med J. 2005; 118: 174 ‐ 176.
dc.identifier.citedreferenceSahin MI, Vurl A, Yuce I, et al. Thyroid leiomyosarcoma: presentation of two cases and review of the literature. Braz J Otorhinolaryngol. 2016; 82: 715 ‐ 721.
dc.identifier.citedreferenceCanu GL, Bulla JS, Lai ML, et al. Primary thyroid leiomyosarcoma: a case report and review of the literature. G Chir. 2018; 39: 51 ‐ 56.
dc.identifier.citedreferenceD’andrea N, Romano V, Mattioli F, et al. Pulmonary artery leiomyosarcoma with thyroid metastases. Monaldi Arch Chest Dis. 2003; 59: 304 ‐ 307.
dc.identifier.citedreferenceBiankin SA, Cachia AR. Leiomyoma of the thyroid gland. Pathology. 1999; 31: 48 ‐ 66.
dc.identifier.citedreferenceThompson LD, Wenig BM, Adair CF, et al. Primary smooth muscle tumors of the thyroid gland. Cancer. 1997; 79: 579 ‐ 587.
dc.identifier.citedreferenceBlack M, Wei XJ, Sun W, et al. Adult rhabdomyoma presenting as thyroid nodule on fine needle aspiration in patient with BIRT‐Hogg‐Dube’ syndrome: case report and literature review. Diagn Cytopathol. 2020; 48: 576 ‐ 580.
dc.identifier.citedreferencePurgina B, Rao UNM, Miettinen M, Pantanowitz L. AIDS‐related EBV‐associated smooth muscle tumors: a review of 64 published cases. Path Res Int. 2011; 10: 561548.
dc.identifier.citedreferenceTaccagni G, Sambade C, Nesland J, Terreni MR, Sobrinho‐Simoes M. Solitary fibrous tumor of the thyroid: clinico‐pathological, immunohistochemical and ultrastructural study of three cases. Virchows Arch A Pathol Anat Histopathol. 1993; 422: 491 ‐ 497.
dc.identifier.citedreferenceMizuuchi Y, Yamamoto H, Nakamura K, et al. Solitary fibrous tumor of the thyroid gland. Med Mol Morphol. 2014; 47: 117 ‐ 122.
dc.identifier.citedreferenceParwani AV, Galindo R, Steinberg D, et al. Solitary fibrous tumor of the thyroid: cytopathologic findings and differential diagnosis. Diagn Cytopathol. 2003; 28: 213 ‐ 216.
dc.identifier.citedreferenceDoyle LA, Vivero M, Fletcher CD, Mertens F, Hornick JL. Nuclear expression of STAT6 distinguishes solitary fibrous tumor from histologic mimics. Mod Pathol. 2014; 27: 390 ‐ 395.
dc.identifier.citedreferenceDemicco EG, Wagner MJ, Maki RG, et al. Risk assessment in solitary fibrous tumors: validation and refinement of a risk stratification model. Mod Pathol. 2017; 30: 1433 ‐ 1442.
dc.identifier.citedreferenceWestra WH, Gerald WL, Rosai J. Solitary fibrous tumor. Consistent CD34 immunoreactivity and occurrence in the orbit. Am J Surg Pathol. 1994; 18: 992 ‐ 998.
dc.identifier.citedreferenceSuster D, Michal M, Nishino M, et al. Papillary thyroid carcinoma with prominent myofibroblastic stromal component: clinicopathologic, immunohistochemical and next‐generation sequencing study of seven cases. Mod Pathol. 2020; 33: 1702 ‐ 1711.
dc.identifier.citedreferenceYu L, Yang SJ. Primary Follicular dendritic cell Sarcoma of the thyroid gland coexisting with hashimoto thyroiditis. Int J Surg Pathol. 2011; 19: 502 ‐ 505.
dc.identifier.citedreferenceFonseca R, Yamakawa M, Nagkamura S, et al. Follicular dendritic cell sarcoma and interdigitating reticulum cell sarcoma: a review. Am J Hematol. 1998; 59: 161 ‐ 167.
dc.identifier.citedreferenceMonda L, Warnke R, Rosai J. A primary lymph node malignancy with features suggestive of dendritic reticulum cell differentiation. A report of 4 cases. Am J Pathol. 1986; 122: 562 ‐ 572.
dc.identifier.citedreferenceJabbour MN, Fedda FA, Tawil AN, Shabb NS, Boulos FI. Follicular dendritic cell sarcoma of the head and neck expressing thyroid transcription factor‐1: a case report with clinocopathologic and immunohistochemical literature review. Appl Immunohistochem Mol Morphol. 2014; 22: 705 ‐ 712.
dc.identifier.citedreferenceDavila J, Starr JS, Attia S, et al. Comprehensive genomic profiling of a rare thyroid follicular dendritic cell sarcoma. Rare Tumors. 2017; 9: 6834 ‐ 6837.
dc.identifier.citedreferenceStarr JS, Attia S, Joseph RW, et al. Follicular dendritic cell sarcoma presenting as a thyroid mass. J Clin Oncol. 2015; 33: e74 ‐ e76.
dc.identifier.citedreferenceGalati LT, Barnes EL, Myers EN. Dendritic cell sarcoma of the thyroid. Head Neck. 1999; 21: 273 ‐ 275.
dc.identifier.citedreferenceChetty R, Clark SP, Dowlin JP. Leiomyosarcoma of the thyroid: immunohistochemical and ultrastructural study. Pathology. 1993; 25: 203 ‐ 205.
dc.identifier.citedreferenceGriffin GK, Sholl LM, Lindeman NI, Fletcher CD, Hornick JL. Targeted genomic sequencing of follicular dendritic cell sarcoma reveals recurrent alterations in NF‐κB regulatory genes. Mod Pathol. 2016; 29: 67 ‐ 74.
dc.identifier.citedreferencePusztaszeri M, Sauder K, Cibas ES, Faquin WC. Fine‐needle aspiration of primary Langerhans cell histiocytosis of the thyroid gland, a potential mimic of papillary thyroid carcinoma. Acta Cytol. 2013; 57: 406 ‐ 412.
dc.identifier.citedreferenceHarmon CM, Brown N. Langerhans cell histiocytosis: a clinicopathologic review and molecular pathogenetic update. Arch Pathol Lab Med. 2015; 139: 1211 ‐ 1214.
dc.identifier.citedreferencePandyaraj RA, Sathik M, Masoodu K, et al. Langerhans cell histiocytosis of thyroid—a diagnostic dilemma. Indian J Surg. 2015; 77: 49 ‐ 51.
dc.identifier.citedreferenceSaqi A, Kuker AP, Ebner SA, et al. Langerhans cell histiocytosis: diagnosis on thyroid aspirate and review of the literature. Head Neck Pathol. 2015; 9: 496 ‐ 502.
dc.identifier.citedreferenceCeyran AB, Senol S, Bayraktar B, et al. Langerhans cell histiocytosis of the thyroid with multiple cervical lymph node involvement accompanying metastatic thyroid papillary carcinoma. Case Rep Pathol. 2014: 184237.
dc.identifier.citedreferenceXia CX, Li R, Wang ZH, et al. A rare cause of goiter: Langerhans cell histiocytosis of the thyroid. Endocr J. 2012; 59: 47 ‐ 54.
dc.identifier.citedreferenceGul OO, Sisman P, Cander S, et al. An unusual case of adult‐onset multi‐systemic Langerhans cell histiocytosis with perianal and incident thyroid involvement. Endocrinol Diabetes Metab Case Rep. 2017; 2: 16‐0087.
dc.identifier.citedreferenceBehrens RJ, Levi AW, Westra WH, Dutta D, Cooper DS, Behrens RJ, et al. Langerhans cell histiocytosis of the thyroid: a report of two cases and review of the literature. Thyroid. 2001; 11: 697 ‐ 705.
dc.identifier.citedreferencePatten DK, Wani Z, Tolley N, Patten DK, et al. Solitary Langerhans histiocytosis of the thyroid gland: a case report and literature review. Head Neck Pathol. 2012; 6: 279 ‐ 289.
dc.working.doiNOen
dc.owningcollnameInterdisciplinary and Peer-Reviewed


Files in this item

Name:
cncy22404_am.pdf
Size:
1.949MB
Format:
PDF
View/Open
Name:
cncy22404.pdf
Size:
4.933MB
Format:
PDF
View/Open

Show simple item record

Remediation of Harmful Language

The University of Michigan Library aims to describe library materials in a way that respects the people and communities who create, use, and are represented in our collections. Report harmful or offensive language in catalog records, finding aids, or elsewhere in our collections anonymously through our metadata feedback form. More information at Remediation of Harmful Language.

Accessibility

If you are unable to use this file in its current format, please select the Contact Us link and we can modify it to make it more accessible to you.