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Uterine Leiomyosarkomların Leiomyomlardan Ayırıcı Tanısında Ameliyat Öncesi Laboratuvar Değerlendirmelerinin Önemi

Yıl 2025, Cilt: 15 Sayı: 3, 283 - 294, 15.09.2025

Öz

Amaç: Uterin leiomyosarkomun (ULMS) preoperatif tanısı zordur çünkü hastalık dejenere uterin leiomyoma (DULM) ve iyi huylu leiomyomu (ULM) taklit edebilir. Bu çalışmanın amacı, uterin ULMS, DULM ve ULM'yi ayırt etmede preoperatif klinik özelliklerin ve hematolojik parametrelerin rolünü araştırmaktır. Özellikle genç yaş grubunda sıklıkla semptomatik olan ve operasyon planlanan olguların leiomyoma kitlesinin maling yönde değişimi öngörülerek gerekli cerrahi ve medikal tedavilerinin eksiksiz yapılmasının sağlanması planıyla bu çalışma literatür tartışması eşliğinde planlanmıştır.
Materiyal ve yöntemler: 2022-2025 arasında jinekolojik onkoloji merkezlerinde uterin kitle nedeniyle operasyon geçiren 336 hastanın klinik kayıtlarını retrospektif olarak inceledik. Uterin benign leiomyoma tanısı alan 272 (benign) (ULM) (grup 1), malignite dışlanamayan 43 (presumed malign or dejenere uterin leiomyoma) (DULM) (grup 2) ve 21 leiomyosarkoma (malign) (ULMS) (grup 3) olgu çalışmaya dahil edildi.
Uterin leiomyosarkoma grubunda ve kontrol gruplarında (ULM, DULM) hastaların demografik, klinik, patolojik verileri, ultrasonografik özellikleri, laboratuvar testleri ve cerrahi operasyon yöntemleri retrospektif olarak alındı. Ultrasonografik özellikler arasında uterusun en büyük çapı, miyom sayısı ve en büyük miyom çapı yer aldı.
Laboratuvar testleri arasında hemoglobin, hematokrit, lökosit, nötrofil sayısı, lenfosit, trombosit, mean platelet volume (MPV), Troid stimulan hormon (TSH), açlık kan glukozu (FBG), cancer antigen-125 (CA-125), carcino-embrionic antigen (CEA), C-reactive protein (CRP), cancer antigen 15-3 (CA-15-3), Eritrosit sedimentasyon hızı (ESR), Alpha-fetoprotein (AFP), cancer antigen (CA-19-9) ve serum laktat dehidrogenaz (LDH) seviyesi yer aldı. Ultrasonografi ve laboratuvar testleri ameliyattan önceki bir ay içinde yapıldı.
Bulgular: Olguların yaş ortalaması 47,2±12,6 iken BMI oranları 26,1±6 idi. Grup I ve II arasında nötrofil 3650 (1560-12150)/4200 ( 1990-12490)ve NLR (nötrofil/lenfosit oranı) 1,44 (0,52-7,31)/1,85 (0,74-6,51) oranları açısından istatistiksel anlamlı farklılık izlendi (sırasıyla p değerleri: 0.029, 0.004). 3 grup arasında biokimyasal değerlerin postHoc analizi yapıldığında ise CRP (C reactive protein) değerleri grup I de 4,6 (1,1-26,3) iken grup II de ise 7,3 (1,8-45,1) olup iki grup arasında istatistiksel anlamlı farklılık izlendi (p değeri:0,029). ESR (eritrosit sedimentasyon oranı) açısında grup I: 11,2 (6,4-29,2), Grup II: 20,3 (8,5-32,2) ve grup III ise 22,8 (17,5-30,8) değerleri açısından grup I ile II ve I ile III arasında istatistiksel olarak anlamlı farklılık izlendi (sırasıyla p değerleri: <0,001, <0,001). LDH (laktat dehidrogenaz) düzeyleri grup I de 182 (112-295), grup II de 196 (126-381) ve grup III te ise 246 (164-373) olup her üç grubun karşılaştırılmasında grup I ile II, I ve III ve II ile III arasında istatistiksel olarak anlamlı farklılık izlendi (sırasıyla p değerleri: <0,001, <0,001, <0,001).
Sonuç: Preoperatif dönemde Bening uterin leiomyomaları, dejenere uterin leiomyoma ve malign uterin leiomyosarkomalardan ayırıcı tanısında özellikle ESR ve LDH düzeylerinin ayrıcı tanıda önemli olduğu unutulmamalıdır. Cerrahi sonrası histopatolojik incelemenin altın standart olduğu ancak özellikle çok merkezli prospektif çalışmalar ile preoperatif laboratuar belirtleçlerinin de ayırıcı tanıdaki değeri daha net ortaya konulabilir.

Kaynakça

  • 1. Nishigaya Y, Kobayashi Y, Matsuzawa Y, Hasegawa K, Fukasawa I, Watanabe Y, et al. Diagnostic value of combination serum assay of lactate dehydrogenase, D-dimer, and C-reactive protein for uterine leiomyosarcoma. J Obstet Gynaecol Res. 2019;45(1):189-94.
  • 2. Cui RR, Wright JD. Risk of occult uterine sarcoma in presumed uterine fibroids. Clin Obstet Gynecol. 2016;59(1):103-8.
  • 3. Cho HY, Kim K, Kim YB, No JH. Differential diagnosis between uterine sarcoma and leiomyoma using preoperative clinical characteristics. J Obstet Gynaecol Res. 2016;42(3):313-8.
  • 4. Zhang G, Yu X, Zhu L, Fan Q, Shi H, Lang J. Preoperative clinical characteristics scoring system for differentiating uterine leiomyosarcoma from fibroid. BMC Cancer. 2020;20(1):514.
  • 5. Eo WK, Kim KH, Park EJ, Kim HY, Kim HB, Koh SB, et al. Diagnostic accuracy of inflammatory markers for distinguishing malignant and benign ovarian masses. J Cancer. 2018;9(7):1165-72.
  • 6. Kwon BS, Jeong DH, Byun JM, Lee TH, Choi KU, Song YJ, et al. Prognostic value of preoperative lymphocyte-monocyte ratio in patients with ovarian clear cell carcinoma. J Cancer. 2018;9(7):1127- 34.
  • 7. Jeong MJ, Park JH, Hur SY, Kim CJ, Nam HS, Lee YS. Preoperative neutrophil-to-lymphocyte ratio as a prognostic factor in uterine sarcoma. J Clin Med. 2020;9(9):2898.
  • 8. U.S. Food and Drug Administration. Updated laparoscopic uterine power morcellation in hysterectomy and myomectomy: FDA safety communication. Silver Spring (MD): U.S. Food and Drug Administration; 2014. [Erişim: 29.07.2025]. Erişim adresi: https:// www.fda.gov/media/88836/download
  • 9. Gallicchio L, Harvey LA, Kjerulff KH. Fear of cancer among women undergoing hysterectomy for benign conditions. Psychosom Med. 2005;67(3):420-4.
  • 10. Ricci S, Stone RL, Fader AN. Uterine leiomyosarcoma: epidemiology, contemporary treatment strategies and the impact of uterine morcellation. Gynecol Oncol. 2017;145(1):208-16.
  • 11. Skorstad M, Kent A, Lieng M. Uterine leiomyosarcoma–incidence, treatment, and the impact of morcellation. A nationwide cohort study. Acta Obstet Gynecol Scand. 2016;95(9):984-90.
  • 12. Köhler G, Vollmer M, Nath N, Hessler PA, Dennis K, Lehr A, et al. Benign uterine mass-discrimination from leiomyosarcoma by a preoperative risk score: a multicenter cohort study. Arch Gynecol Obstet. 2019;300(6):1719-27.
  • 13. Ghosh S, Naftalin J, Imrie R, Hoo WL. Natural History of Uterine Fibroids: A Radiological Perspective. Curr Obstet Gynecol Rep. 2018;7:117-21.
  • 14. Mavrelos D, Ben-Nagi J, Holland T, Hoo W, Naftalin J, Jurkovic D. The natural history of fibroids. Ultrasound Obstet Gynecol. 2010;35(2):238-42.
  • 15. Li Q, Zhong J, Yi D, Deng G, Liu Z, Wang W. Assessing the risk of rapid fibroid growth in patients with asymptomatic solitary uterine myoma using a multivariate prediction model. Ann Transl Med. 2021;9(5):370.
  • 16. Valzacchi GMR, Rosas P, Uzal M, Gil SJ, Viglierchio VT. Incidence of leiomyosarcoma at surgery for presumed uterine myomas in different age groups. J Minim Invasive Gynecol. 2020;27(4):926-9.
  • 17. Singh N, Al-Ruwaisan M, Batra A, Itani D, Ghatage P. Factors affecting overall survival in premenopausal women with uterine leiomyosarcoma: a retrospective analysis with long-term follow-up. J Obstet Gynaecol Can. 2020;42(12):1483-8.
  • 18. Kadhel P, Borja de Mozota D, Simon P, Toto T, Jermidi C, Ayhan G. Leiomyomas in an African Caribbean hysterectomy population considered to be ethnically related to African Americans. J Gynecol Obstet Hum Reprod. 2020;49:101654.
  • 19. Brohl AS, Li L, Andikyan V, Običan SG, Cioffi A, Hao K, et al. Agestratified risk of unexpected uterine sarcoma following surgery for presumed benign leiomyoma. Oncologist. 2015;20(4):433-9.
  • 20. Miao P, Sheng S, Sun X, Liu J, Huang G. Lactate dehydrogenase A in cancer: a promising target for diagnosis and therapy. IUBMB Life. 2013;65(11):904-10.
  • 21. Wang ZY, Loo TY, Shen JG, Wang N, Wang DM, Yang DP, et al. LDH-A silencing suppresses breast cancer tumorigenicity through induction of oxidative stress mediated mitochondrial pathway apoptosis. Breast Cancer Res Treat. 2012;131(3):791-800.
  • 22. Seki K, Hoshihara T, Nagata I. Leiomyosarcoma of the uterus: ultrasonography and serum lactate dehydrogenase level. Gynecol Obstet Investig. 1992;33(2):114-8.
  • 23. Nagai T, Takai Y, Akahori T, Ishida H, Hanaoka T, Uotani T, et al. Highly improved accuracy of the revised PREoperative sarcoma score (rPRESS) in the decision of performing surgery for patients presenting with a uterine mass. SpringerPlus. 2015;4:520.
  • 24. Kusunoki S, Terao Y, Ujihira T, Fujino K, Kaneda H, Kimura M, et al. Efficacy of PET/CT to exclude leiomyoma in patients with lesions suspicious for uterine sarcoma on MRI. Taiwan J Obstet Gynecol. 2017;56(4):508-13.
  • 25. Goto A, Takeuchi S, Sugimura K, Maruo T. Usefulness of Gd-DTPA contrast enhanced dynamic MRI and serum determination of LDH and its isozymes in the differential diagnosis of leiomyosarcoma from degenerated leiomyoma of the uterus. Int J Gynecol Cancer. 2002;12(3):354-61.
  • 26. Zhang F, Liu Y, Quan Q, Meng Y, Mu X. Diagnostic value of preoperative CA125, LDH and HE4 for leiomyosarcoma of the female reproductive system. Cancer Manag Res. 2021;13:4657-64.
  • 27. Lawlor H, Ward A, Maclean A, Lane S, Adishesh M, Taylor S, et al. Developing a preoperative algorithm for the diagnosis of uterine leiomyosarcoma. Diagnostics. 2020;23;10(10):735.
  • 28. DiSaia PJ, Haverback BJ, Dyce BJ, Morrow CP. Carcinoembryonic antigen in patients with gynecologic malignancies. Am J Obstet Gynecol. 1975;121(2):159-63.
  • 29. Hoskins PJ, Le N. Preoperative tumor markers at diagnosis in women with malignant mixed müllerian tumors/carcinosarcoma of the uterus. Int J Gynecol Cancer. 2008;18(6):1200-1.
  • 30. Thomakos N, Rodolakis A, Zagouri F, Zacharakis D, Sotiropoulou M, Akrivos N, et al. Serum CA 125, CA 15-3, CEA, and CA 19-9: a prognostic factor for uterine carcinosarcomas? Arch Gynecol Obstet. 2013;287(1):97-102.
  • 31. Suh DS, Song YJ, Roh HJ, Lee SH, Jeong DH, Lee TH, et al. Preoperative blood inflammatory markers for the differentiation of uterine leiomyosarcoma from leiomyoma. Cancer Manag Res. 2021;13:5001-11.
  • 32. Kim HS, Han KH, Chung HH, Kim JW, Park NH, Song YS, et al. Neutrophil to lymphocyte ratio for preoperative diagnosis of uterine sarcomas: a case-matched comparison. Eur J Surg Oncol. 2010;36(7):691-8.
  • 33. Jiang M, Ma S, Hua Z, Zhao Z, Gao S. Prognostic value of pretreated blood inflammatory markers in patients with bone sarcoma: a metaanalysis. Dis Markers. 2021;2021:8839512.
  • 34. Liu G, Ke LC, Sun SR. Prognostic value of pretreatment neutrophilto-lymphocyte ratio in patients with soft tissue sarcoma: a metaanalysis. Medicine. 2018;97(36):e12176.
  • 35. Chang MY, Tsai FB, Soong YK. Infarcted intramural uterine leiomyomata during buserelin acetate treatment. Changgeng Yi Xue Za Zhi. 1993;16(2):129-32.
  • 36. Onishi S, Hojo N, Sakai I, Matsumoto T, Watanabe A, Miyazaki T, et al. Secondary amyloidosis and eosinophilia in a patient with uterine leiomyosarcoma. Jpn J Clin Oncol. 2005;35(10):617-21.

The Importance of Preoperative Laboratory Evaluations in the Differential Diagnosis of Uterine Leiomyosarcomas from Leiomyomas

Yıl 2025, Cilt: 15 Sayı: 3, 283 - 294, 15.09.2025

Öz

Background: Preoperative diagnosis of uterine leiomyosarcomas (ULMS) is challenging, as it may mimic degenerative uterine leiomyosarcoma (DULM) and benign uterine leiomyoma (ULM). This study investigates the role of preoperative clinical features and hematological parameters in the differential diagnosis of ULMS, DULM, and ULM. In light of the literature, this study was planned to perform the required surgical and medical treatments correctly and completely by predicting the malignant transformation of the leiomyoma mass in patients who are usually young, symptomatic, and planning to undergo surgery.
Methods: Clinical records of 336 patients who underwent surgery due to uterine mass lesions in gynecological oncology clinics between 2022 and 2025 were retrospectively analyzed. A total of 272 patients diagnosed with benign uterine leiomyoma (Group 1, benign, ULM), 43 patients in whom malignancy could not be ruled out (Group 2, presumed malignant or degenerated uterine leiomyoma, DULM), and 21 patients with leiomyosarcoma (Group 3, malignant, ULMS) were included in the study.
In the uterine leiomyosarcoma group and control groups (ULM, DULM), data about demographic, clinical, pathological, and ultrasonography features, laboratory tests, and surgical methods used were obtained retrospectively. Ultrasonography features included the largest diameter of the uterus, the number of myomas, and the diameter of the largest myoma.
Laboratory tests included hemoglobin (HGB), hematocrit (HTC), white blood cell (WBC), neutrophil count, lymphocyte, neutrophil to lymphocyte ratio (NLR), platelet count (PLT), mean platelet volume (MPV), thyroid stimulating hormone (TSH), fasting blood glucose (FBG), cancer antigen-125 (CA-125), carcino-embryonic antigen (CEA), C-reactive protein (CRP), cancer antigen 15-3 (CA-15-3), erythrocyte sedimentation rate (ESR), alpha-fetoprotein (AFP), cancer antigen 19-9 (CA-19-9), and serum lactate dehydrogenase (LDH) level. Ultrasonography and laboratory tests were performed within one month before surgery.
Results: The mean age of the patients was 47.2±12.6 years, and the BMI was 26.1±6 kg/m2. A statistically significant difference was found between Group I and II with regard to neutrophil count 3650 (1560-12150)/4200 (1990-12490) and NLR 1,44 (0,52-7,31)/1,85 (0,74-6,51) (p: 0.029 and 0.004, respectively). In post hoc analysis of biochemical values among three groups, CRP values were 4,6 (1,1-26,3) in Group I, they were 7,3 (1,8-45,1) in Group II, and the difference was statistically significant (p: 0,029). A statistically significant difference was found between Group I and II, and between Group I and III (Group I: 11,2 (6,4-29,2), Group II: 20,3 (8,5-32,2), and Group III: 22,8 (17,5-30,8) (p: <0,001 and <0,001, respectively). LDH values were 182 (112-295) in Group I, 196 (126-381) in Group II, and 246 (164-373) in Group III, and a statistically significant difference was found between Group I and II, between Group I and III, and between Group II and III (p: <0,001, <0,001, and <0,001, respectively).
Conclusion: It should be kept in mind that preoperative ESR and LDH values are significant in the differential diagnosis of benign uterine leiomyoma, degenerative uterine leiomyoma, and malignant uterine leiomyosarcoma. Postoperative histopathological examination is the gold standard; however, the value of preoperative laboratory biomarkers may be revealed through multi-center prospective studies.

Etik Beyan

Bu çalışma Helsinki Bildirgesi'nde açıklanan etik standartlara uygun olarak yürütüldü ve lokal etik komitesinden 18/04/2025 tarih ve 4/6 sayılı numara ile etik kurul onayı alındı.

Destekleyen Kurum

Osmaniye Devlet Hastanesi

Teşekkür

Osmaniye Devlet Hastanesi ve Özel Park Hastanesi tüm sağlık çalışanlarına teşekkür ediyoruz.

Kaynakça

  • 1. Nishigaya Y, Kobayashi Y, Matsuzawa Y, Hasegawa K, Fukasawa I, Watanabe Y, et al. Diagnostic value of combination serum assay of lactate dehydrogenase, D-dimer, and C-reactive protein for uterine leiomyosarcoma. J Obstet Gynaecol Res. 2019;45(1):189-94.
  • 2. Cui RR, Wright JD. Risk of occult uterine sarcoma in presumed uterine fibroids. Clin Obstet Gynecol. 2016;59(1):103-8.
  • 3. Cho HY, Kim K, Kim YB, No JH. Differential diagnosis between uterine sarcoma and leiomyoma using preoperative clinical characteristics. J Obstet Gynaecol Res. 2016;42(3):313-8.
  • 4. Zhang G, Yu X, Zhu L, Fan Q, Shi H, Lang J. Preoperative clinical characteristics scoring system for differentiating uterine leiomyosarcoma from fibroid. BMC Cancer. 2020;20(1):514.
  • 5. Eo WK, Kim KH, Park EJ, Kim HY, Kim HB, Koh SB, et al. Diagnostic accuracy of inflammatory markers for distinguishing malignant and benign ovarian masses. J Cancer. 2018;9(7):1165-72.
  • 6. Kwon BS, Jeong DH, Byun JM, Lee TH, Choi KU, Song YJ, et al. Prognostic value of preoperative lymphocyte-monocyte ratio in patients with ovarian clear cell carcinoma. J Cancer. 2018;9(7):1127- 34.
  • 7. Jeong MJ, Park JH, Hur SY, Kim CJ, Nam HS, Lee YS. Preoperative neutrophil-to-lymphocyte ratio as a prognostic factor in uterine sarcoma. J Clin Med. 2020;9(9):2898.
  • 8. U.S. Food and Drug Administration. Updated laparoscopic uterine power morcellation in hysterectomy and myomectomy: FDA safety communication. Silver Spring (MD): U.S. Food and Drug Administration; 2014. [Erişim: 29.07.2025]. Erişim adresi: https:// www.fda.gov/media/88836/download
  • 9. Gallicchio L, Harvey LA, Kjerulff KH. Fear of cancer among women undergoing hysterectomy for benign conditions. Psychosom Med. 2005;67(3):420-4.
  • 10. Ricci S, Stone RL, Fader AN. Uterine leiomyosarcoma: epidemiology, contemporary treatment strategies and the impact of uterine morcellation. Gynecol Oncol. 2017;145(1):208-16.
  • 11. Skorstad M, Kent A, Lieng M. Uterine leiomyosarcoma–incidence, treatment, and the impact of morcellation. A nationwide cohort study. Acta Obstet Gynecol Scand. 2016;95(9):984-90.
  • 12. Köhler G, Vollmer M, Nath N, Hessler PA, Dennis K, Lehr A, et al. Benign uterine mass-discrimination from leiomyosarcoma by a preoperative risk score: a multicenter cohort study. Arch Gynecol Obstet. 2019;300(6):1719-27.
  • 13. Ghosh S, Naftalin J, Imrie R, Hoo WL. Natural History of Uterine Fibroids: A Radiological Perspective. Curr Obstet Gynecol Rep. 2018;7:117-21.
  • 14. Mavrelos D, Ben-Nagi J, Holland T, Hoo W, Naftalin J, Jurkovic D. The natural history of fibroids. Ultrasound Obstet Gynecol. 2010;35(2):238-42.
  • 15. Li Q, Zhong J, Yi D, Deng G, Liu Z, Wang W. Assessing the risk of rapid fibroid growth in patients with asymptomatic solitary uterine myoma using a multivariate prediction model. Ann Transl Med. 2021;9(5):370.
  • 16. Valzacchi GMR, Rosas P, Uzal M, Gil SJ, Viglierchio VT. Incidence of leiomyosarcoma at surgery for presumed uterine myomas in different age groups. J Minim Invasive Gynecol. 2020;27(4):926-9.
  • 17. Singh N, Al-Ruwaisan M, Batra A, Itani D, Ghatage P. Factors affecting overall survival in premenopausal women with uterine leiomyosarcoma: a retrospective analysis with long-term follow-up. J Obstet Gynaecol Can. 2020;42(12):1483-8.
  • 18. Kadhel P, Borja de Mozota D, Simon P, Toto T, Jermidi C, Ayhan G. Leiomyomas in an African Caribbean hysterectomy population considered to be ethnically related to African Americans. J Gynecol Obstet Hum Reprod. 2020;49:101654.
  • 19. Brohl AS, Li L, Andikyan V, Običan SG, Cioffi A, Hao K, et al. Agestratified risk of unexpected uterine sarcoma following surgery for presumed benign leiomyoma. Oncologist. 2015;20(4):433-9.
  • 20. Miao P, Sheng S, Sun X, Liu J, Huang G. Lactate dehydrogenase A in cancer: a promising target for diagnosis and therapy. IUBMB Life. 2013;65(11):904-10.
  • 21. Wang ZY, Loo TY, Shen JG, Wang N, Wang DM, Yang DP, et al. LDH-A silencing suppresses breast cancer tumorigenicity through induction of oxidative stress mediated mitochondrial pathway apoptosis. Breast Cancer Res Treat. 2012;131(3):791-800.
  • 22. Seki K, Hoshihara T, Nagata I. Leiomyosarcoma of the uterus: ultrasonography and serum lactate dehydrogenase level. Gynecol Obstet Investig. 1992;33(2):114-8.
  • 23. Nagai T, Takai Y, Akahori T, Ishida H, Hanaoka T, Uotani T, et al. Highly improved accuracy of the revised PREoperative sarcoma score (rPRESS) in the decision of performing surgery for patients presenting with a uterine mass. SpringerPlus. 2015;4:520.
  • 24. Kusunoki S, Terao Y, Ujihira T, Fujino K, Kaneda H, Kimura M, et al. Efficacy of PET/CT to exclude leiomyoma in patients with lesions suspicious for uterine sarcoma on MRI. Taiwan J Obstet Gynecol. 2017;56(4):508-13.
  • 25. Goto A, Takeuchi S, Sugimura K, Maruo T. Usefulness of Gd-DTPA contrast enhanced dynamic MRI and serum determination of LDH and its isozymes in the differential diagnosis of leiomyosarcoma from degenerated leiomyoma of the uterus. Int J Gynecol Cancer. 2002;12(3):354-61.
  • 26. Zhang F, Liu Y, Quan Q, Meng Y, Mu X. Diagnostic value of preoperative CA125, LDH and HE4 for leiomyosarcoma of the female reproductive system. Cancer Manag Res. 2021;13:4657-64.
  • 27. Lawlor H, Ward A, Maclean A, Lane S, Adishesh M, Taylor S, et al. Developing a preoperative algorithm for the diagnosis of uterine leiomyosarcoma. Diagnostics. 2020;23;10(10):735.
  • 28. DiSaia PJ, Haverback BJ, Dyce BJ, Morrow CP. Carcinoembryonic antigen in patients with gynecologic malignancies. Am J Obstet Gynecol. 1975;121(2):159-63.
  • 29. Hoskins PJ, Le N. Preoperative tumor markers at diagnosis in women with malignant mixed müllerian tumors/carcinosarcoma of the uterus. Int J Gynecol Cancer. 2008;18(6):1200-1.
  • 30. Thomakos N, Rodolakis A, Zagouri F, Zacharakis D, Sotiropoulou M, Akrivos N, et al. Serum CA 125, CA 15-3, CEA, and CA 19-9: a prognostic factor for uterine carcinosarcomas? Arch Gynecol Obstet. 2013;287(1):97-102.
  • 31. Suh DS, Song YJ, Roh HJ, Lee SH, Jeong DH, Lee TH, et al. Preoperative blood inflammatory markers for the differentiation of uterine leiomyosarcoma from leiomyoma. Cancer Manag Res. 2021;13:5001-11.
  • 32. Kim HS, Han KH, Chung HH, Kim JW, Park NH, Song YS, et al. Neutrophil to lymphocyte ratio for preoperative diagnosis of uterine sarcomas: a case-matched comparison. Eur J Surg Oncol. 2010;36(7):691-8.
  • 33. Jiang M, Ma S, Hua Z, Zhao Z, Gao S. Prognostic value of pretreated blood inflammatory markers in patients with bone sarcoma: a metaanalysis. Dis Markers. 2021;2021:8839512.
  • 34. Liu G, Ke LC, Sun SR. Prognostic value of pretreatment neutrophilto-lymphocyte ratio in patients with soft tissue sarcoma: a metaanalysis. Medicine. 2018;97(36):e12176.
  • 35. Chang MY, Tsai FB, Soong YK. Infarcted intramural uterine leiomyomata during buserelin acetate treatment. Changgeng Yi Xue Za Zhi. 1993;16(2):129-32.
  • 36. Onishi S, Hojo N, Sakai I, Matsumoto T, Watanabe A, Miyazaki T, et al. Secondary amyloidosis and eosinophilia in a patient with uterine leiomyosarcoma. Jpn J Clin Oncol. 2005;35(10):617-21.
Toplam 36 adet kaynakça vardır.

Ayrıntılar

Birincil Dil İngilizce
Konular Cerrahi Onkoloji, Jinekolojik Onkoloji Cerrahisi, Kadın Hastalıkları ve Doğum
Bölüm Orjinal Çalışma
Yazarlar

Ferhat Çetin 0000-0002-8613-2711

İlkan Kayar 0000-0001-6385-4730

Özer Birge 0000-0002-1939-3743

Yayımlanma Tarihi 15 Eylül 2025
Gönderilme Tarihi 28 Mayıs 2025
Kabul Tarihi 19 Temmuz 2025
Yayımlandığı Sayı Yıl 2025 Cilt: 15 Sayı: 3

Kaynak Göster

APA Çetin, F., Kayar, İ., & Birge, Ö. (2025). The Importance of Preoperative Laboratory Evaluations in the Differential Diagnosis of Uterine Leiomyosarcomas from Leiomyomas. Bozok Tıp Dergisi, 15(3), 283-294.
AMA Çetin F, Kayar İ, Birge Ö. The Importance of Preoperative Laboratory Evaluations in the Differential Diagnosis of Uterine Leiomyosarcomas from Leiomyomas. Bozok Tıp Dergisi. Eylül 2025;15(3):283-294.
Chicago Çetin, Ferhat, İlkan Kayar, ve Özer Birge. “The Importance of Preoperative Laboratory Evaluations in the Differential Diagnosis of Uterine Leiomyosarcomas from Leiomyomas”. Bozok Tıp Dergisi 15, sy. 3 (Eylül 2025): 283-94.
EndNote Çetin F, Kayar İ, Birge Ö (01 Eylül 2025) The Importance of Preoperative Laboratory Evaluations in the Differential Diagnosis of Uterine Leiomyosarcomas from Leiomyomas. Bozok Tıp Dergisi 15 3 283–294.
IEEE F. Çetin, İ. Kayar, ve Ö. Birge, “The Importance of Preoperative Laboratory Evaluations in the Differential Diagnosis of Uterine Leiomyosarcomas from Leiomyomas”, Bozok Tıp Dergisi, c. 15, sy. 3, ss. 283–294, 2025.
ISNAD Çetin, Ferhat vd. “The Importance of Preoperative Laboratory Evaluations in the Differential Diagnosis of Uterine Leiomyosarcomas from Leiomyomas”. Bozok Tıp Dergisi 15/3 (Eylül2025), 283-294.
JAMA Çetin F, Kayar İ, Birge Ö. The Importance of Preoperative Laboratory Evaluations in the Differential Diagnosis of Uterine Leiomyosarcomas from Leiomyomas. Bozok Tıp Dergisi. 2025;15:283–294.
MLA Çetin, Ferhat vd. “The Importance of Preoperative Laboratory Evaluations in the Differential Diagnosis of Uterine Leiomyosarcomas from Leiomyomas”. Bozok Tıp Dergisi, c. 15, sy. 3, 2025, ss. 283-94.
Vancouver Çetin F, Kayar İ, Birge Ö. The Importance of Preoperative Laboratory Evaluations in the Differential Diagnosis of Uterine Leiomyosarcomas from Leiomyomas. Bozok Tıp Dergisi. 2025;15(3):283-94.
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