Dergiler / Annals of Medical Research / 2022 / Cilt: 29 - Sayı: 1

Novel immunohistochemical marker in the differential diagnosis of sex cord-stromal tumors: SF-1

Sayfa
36–40
Yayın Tarihi
2022-10-12
DOI
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Conclusion: Our data shows that SF-1 is a nuclear, reliable and surrogate marker for all SCSTs, and can be used routinely.

📌 3 Maddede Bu Makale

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Amaç & Hipotez:Aim: Sex cord-stromal tumors are relatively uncommon tumors which constitute approximately 8% of all primary ovarian neoplasms.
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Temel Bulgular & Veri:SF-1 is known as a promising immunohistochemical marker in the differentiation of SCST from non-SCST ovarian tumors.
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Sonuç & Katkı:Conclusion: Our data shows that SF-1 is a nuclear, reliable and surrogate marker for all SCSTs, and can be used routinely.
🔬Tür:Araştırma Makalesi
📍Kapsam:Genişletilmiş Akademik Örneklem
⚙️Değişkenler:Alan Parametreleri

Abstract

Aim: Sex cord-stromal tumors are relatively uncommon tumors which constitute approximately 8% of all primary ovarian neoplasms. Morphologic differentiation of non-SCST from SCSTs can be challenging due to microscopic overlap. Immunohistochemistry is beneficial in challenging cases. Inhibin and calretinin have limited sensitivity and specificity, a more sensitive marker is required. SF-1 is known as a promising immunohistochemical marker in the differentiation of SCST from non-SCST ovarian tumors. For this purpose, various non-SCSTs (metastatic and non-metastatic) having morphologic overlap with SCSTs, and multiple SCSTs were stained with SF-1 antibody to elucidate its importance in morphologically challenging cases. Materials and Methods: Twenty-three SCST, 40 non-SCSTs, and an ectopic adrenal tissue were stained with SF-1, and also the percentage and the intensity were scored. SF-1 immunoreactivity was seen in all 23 SCST with varying degrees of intensity and percentage. In contrast, non-SCSTs were negative in all regarding to SF-1. Ectopic adrenal gland tissue and ovarian stroma are positive as non-tumoral lesions. Results: In our series, SF-1 immunoreactivity was seen in all 23 SCST and ectopic adrenal tissue with varying degrees of intensity and diffuseness. In contrast, non-SCSTs were all negative concerning SF-1. In addition; we observed nuclear positivity with SF-1 in 15-75% of the sclerosing stromal tumor cells, whereas inhibin and calretinin were negative in all 4 cases. Conclusion: Our data shows that SF-1 is a nuclear, reliable and surrogate marker for all SCSTs, and can be used routinely.

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Bu Makaleye Atıf Yap

TUNCEL, F., DUMAN, A. A., ÖZDEMİR, D. A., USUBÜTÜN, A. (2022). Novel immunohistochemical marker in the differential diagnosis of sex cord-stromal tumors: SF-1. Annals of Medical Research, Cilt: 29 - Sayı: 1, 36–40. https://ajindex.com/articles/445587

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Kaynakça (15)

  1. Al-Agha OM, Huwait HF, Chow C, et al. FOXL2 is a sensitive and specific marker for sex cord-stromal tumors of the ovary. Am J Surg Pathol 2011;35:484- 94
  2. Stewart CJ, Alexiadis M, Crook ML, Fuller PJ. An immunohistochemical and molecular analysis of problematic and unclassified ovarian sex cordstromal tumors. Hum Pathol 2013;44:2774-81
  3. Zhao C, Barner R, Vinh TN, et al. SF-1 is a diagnostically useful immunohistochemical marker and comparable to other sex cord-stromal tumor markers for the differential diagnosis of ovarian sertoli cell tumor. Int J Gynecol Pathol 2008;27:507-14
  4. Rishi M, Howard LN, Bratthauer GL, Tavassoli FA. Use of monoclonal antibody against human inhibin as a marker for sex cord-stromal tumors of the ovary. Am J Surg Pathol 1997;21:583-9
  5. Movahedi-Lankarani S, Kurman RJ. Calretinin, a more sensitive but less specific marker than alphainhibin for ovarian sex cord-stromal neoplasms: an immunohistochemical study of 215 cases. Am J Surg Pathol 2002;26:1477-83
  6. Yalcin Comert HS, Eyuboglu I, Ersoz S, Aet al. Ovarian masses in children: A single center’s experience. Ann Med Res 2020;27:1465-8
  7. Cevik M, Boleken ME. Characteristics and Approach of Ovarian Masses in Children: Series of 34 Cases. Van Med J 2013;20:57-61
  8. Haroon S, Zia A, Idrees R, et al. Clinicopathological spectrum of ovarian sex cord-stromal tumors; 20 years’ retrospective study in a developing country. J Ovarian Res 2013;6:87
  9. Shim SH, Kim DY, Lee SW, et al. Laparoscopic management of early-stage malignant non-epithelial ovarian tumors: surgical and survival outcomes. Int J Gynecol Cancer 2013; 23:249-55
  10. Jung SE, Rha SE, Lee JM, et al. CT and MRI findings of sex cord-stromal tumor of the ovary. Am J Roentgenol 2005;85:207-15
  11. Rathore R, Arora D, Agarwal S, Sharma S. Correlation of FOXL2 with Inhibin and Calretinin in the Diagnosis of Ovarian Sex Cord Stromal Tumors. Turkish J of Pathology 2016;33:121-8
  12. Deavers MT, Malpica A, Liu J, et al. Ovarian sex cordstromal tumors: an immunohistochemical study including a comparison of calretinin and inhibin. Mod Pathol 2003;16:584-90
  13. McCluggage WG, McKenna M, McBride HA. CD56 is a sensitive and diagnostically useful immunohistochemical marker of ovarian sex cordstromal tumors. Int J Gynecol Pathol 2007;26:322-7
  14. Zhao C, Bratthauer GL, Barner R, Vang R. Diagnostic utility of WT1 immunostaining in ovarian sertoli cell tumor. Am J Surg Pathol 2007;31:1378-86
  15. Zhao C, Vinh TN, McManus