{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2022,3,31]],"date-time":"2022-03-31T01:55:51Z","timestamp":1648691751477},"reference-count":12,"publisher":"Walter de Gruyter GmbH","issue":"1","license":[{"start":{"date-parts":[[2017,3,1]],"date-time":"2017-03-01T00:00:00Z","timestamp":1488326400000},"content-version":"unspecified","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by-nc-nd\/3.0"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2017,3,1]]},"abstract":"<jats:title>Abstract<\/jats:title>\n               <jats:p>\n                  <jats:bold>Objective<\/jats:bold>. Histiocytic sarcoma (HS) is an extraordinary rare tumor and it has an offensive clinical course. HS of the uterine cervix is a far uncommon tumor with just a few cases described so far. Here we presented a case of primary HS of the uterine cervix in a 62-year-old female initially misdiagnosed as large cell non-keratinizing squamous cell carcinoma. To the best of our knowledge, this is the first reported case of HS of the uterine cervix from Iran.<\/jats:p>\n               <jats:p>\n                  <jats:bold>Case report<\/jats:bold>. The patient presented with post-menopausal vaginal bleeding. Further evaluations revealed the presence of a relatively large cervical mass that was sampled. Under the preliminary diagnosis of large cell non-keratinizing squamous cell carcinoma, the patient underwent radical surgery. Postoperative pathological examination confirmed the diagnosis of HS of the uterine cervix. The patient received chemotherapy.<\/jats:p>\n               <jats:p>\n                  <jats:bold>Conclusion<\/jats:bold>. Clinical presentations of HS of the uterine cervix are very similar to more common cervical tumors; as a result its diagnosis relies on immunohistochemical methods. A correct diagnose could lead to the proper and timely treatment.<\/jats:p>","DOI":"10.1515\/rjim-2016-0051","type":"journal-article","created":{"date-parts":[[2016,11,9]],"date-time":"2016-11-09T10:05:10Z","timestamp":1478685910000},"page":"53-56","source":"Crossref","is-referenced-by-count":1,"title":["Primary histiocytic sarcoma of the uterine cervix: an extremely rare entity"],"prefix":"10.1515","volume":"55","author":[{"given":"Fariba","family":"Binesh","sequence":"first","affiliation":[{"name":"Department of Pathology, Shahid Sadoughi University of Medical Sciences, Yazd, Iran (Islamic Republic of)"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Mojgan","family":"Karimi-Zarchi","sequence":"additional","affiliation":[{"name":"Department of Obstetrics and Gynaecology, Shahid Sadoughi University of Medical Sciences, Yazd, Iran (Islamic Republic of)"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Mohammad Reza","family":"Vahidfar","sequence":"additional","affiliation":[{"name":"Medical Oncologist, Yazd, Iran (Islamic Republic of)"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Zahra Kargar","family":"Hadgiabadi","sequence":"additional","affiliation":[{"name":"Department of Pathology, Shahid Sadoughi University of Medical Sciences, Yazd, Iran (Islamic Republic of)"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"374","published-online":{"date-parts":[[2017,3,4]]},"reference":[{"key":"2021040609531995306_j_rjim-2016-0051_ref_001_w2aab2b8b9b1b7b1ab1ab1Aa","doi-asserted-by":"crossref","unstructured":"1. TAKAHASHI E, NAKAMURA S. Histiocytic sarcoma: an updated literature review based on the 2008 WHO classification. J Clin Exp Hematop. 2013; 53(1):1-8.","DOI":"10.3960\/jslrt.53.1"},{"key":"2021040609531995306_j_rjim-2016-0051_ref_002_w2aab2b8b9b1b7b1ab1ab2Aa","unstructured":"2. SWERDLOW SH, CAMPO E, HARRIS NL. WHO Classification of Tumours of Haematopoietic and Lymphoid Tissues. 4th edition. Lyon, France: IARC Press; 2008, 354-357."},{"key":"2021040609531995306_j_rjim-2016-0051_ref_003_w2aab2b8b9b1b7b1ab1ab3Aa","unstructured":"3. JAFFE E S. Histiocytic and dendritic cell neoplasms. In: Jaffe E S, Harris N L, Stein, H et al. (eds), World Health Orgnization classification of tumours: pathology and genetics of tumours of haematopoietic and lymphoid tissues. Lyon: IARC Press 2001: 275-277."},{"key":"2021040609531995306_j_rjim-2016-0051_ref_004_w2aab2b8b9b1b7b1ab1ab4Aa","unstructured":"4. CHEN CJ, WILLIAMS EA, MCANENEY TE, et al. 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VOS JA, ABBONDANZO SL, BAREKMAN CL, ANDRIKO JW, MIETTINEN M, AGUILERA NS. Histiocytic sarcoma: a study of five cases including the histiocyte marker CD163. Mod Pathol. 2005; 18(5):693-704.","DOI":"10.1038\/modpathol.3800346"},{"key":"2021040609531995306_j_rjim-2016-0051_ref_008_w2aab2b8b9b1b7b1ab1ab8Aa","doi-asserted-by":"crossref","unstructured":"8. WANG H, ZHANG J, TAO Q, et al. Flow cytometry used to identify histiocytic sarcoma: A case report. Cytometry B Clin Cytom. 2015, doi: 10.1002\/cyto.b.21262. [Epub ahead of print]","DOI":"10.1002\/cyto.b.21262"},{"key":"2021040609531995306_j_rjim-2016-0051_ref_009_w2aab2b8b9b1b7b1ab1ab9Aa","doi-asserted-by":"crossref","unstructured":"9. SUN W, NORDBERG ML, FOWLER MR. Histiocytic sarcoma involving the central nervous system: clinical, immunohistochemical, and molecular genetic studies of a case with review of the literature. 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