Journals / Haseki Tıp Bülteni / 2012 / Cilt: 50 - Sayı: 1

Sclerosing stromal tumor of the ovary: A case report

Overin sklerozan stromal tümörü: Olgu sunumu

Pages
33–36
DOI
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

A combination of morphological, immunohistochemical, radiological and clinical findings is needed in differentiating the tumor from thecoma, fibroma/fibrosarcoma, lipoid tumors and Krukenberg tumor. (The Me di cal Bul le tin of Ha se ki 2012; 50: 33-6)

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Sclerosing stromal tumor of the ovary is a rare benign ovarian tumor originating from sex-cord stroma.
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Key Findings & Data:Fewer than 120 cases have been described in the English literature.
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Conclusion & Impact:A combination of morphological, immunohistochemical, radiological and clinical findings is needed in differentiating the tumor from thecoma, fibroma/fibrosarcoma, lipoid tumors and Krukenberg tumor. (The Me di cal Bul le tin of Ha se ki 2012; 50: 33-6)
🔬Design:Research Article
📍Scope:2012 Verileri
⚙️Variables:Domain Parameters

Abstract

Sclerosing stromal tumor of the ovary is a rare benign ovarian tumor originating from sex-cord stroma. Fewer than 120 cases have been described in the English literature. In this study, we report a 19-year-old patient, who underwent operation for suspected ovarian cancer due to elevated CA-125 levels and solid ovarian mass detected radiologically. Histologically, it is characterized by pseudolobular patern composed of hypocellular and hypercellular areas with abundant vascular structures. Intraoperative diagnosis of the tumor is extremely important, since it is mostly observed in young patients requiring conservative surgery. To identify its benignancy during intraoperative examination is sufficient for the selection of the appropriate surgical approach. A combination of morphological, immunohistochemical, radiological and clinical findings is needed in differentiating the tumor from thecoma, fibroma/fibrosarcoma, lipoid tumors and Krukenberg tumor. (The Me di cal Bul le tin of Ha se ki 2012; 50: 33-6)

Özet

Overin sklerozan stromal tümörü, seks-kord stroma kaynaklı nadir, benign bir over tümörüdür. İngilizce literatürde 120'den az olgu tanımlanmıştır. Çalışmamızda CA-125 yüksekliği ve radyolojik olarak solid görünümlü over kitlesinden dolayı malignite şüphesi ile opere edilen 19 yaşında olgu sunulmaktadır. Histolojik olarak tümör bol vasküler yapılar ile birlikte hücresel ve hiposellüler alanlardan oluşan karakteristik psödolobüler paterne sahiptir. Konservatif cerrahinin gerekli olduğu genç hastalarda görülmesi nedeniyle sklerozan stromal tümörün intraoperatif patolojik tanısı büyük önem taşır. İntraoperatif incelemede benign yönünde yanıt verilmesi doğru cerrahi girişimin yapılması için yeterlidir. Ayırıcı tanıda yer alan tekom, fibrom-fibrosarkom, lipoid tümörler ve Krukenberg tümöründen ayrımı için morfolojik, immünohistokimyasal, radyolojik ve klinik bulguların kombinasyonu gereklidir. (Ha se ki Tıp Bül te ni 2012; 50: 33-6)

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Cite This Article

SAYILGAN, A. T., FİLİZ, F., ÖZCAN, D. (2012). Sclerosing stromal tumor of the ovary: A case report. Haseki Tıp Bülteni, Cilt: 50 - Sayı: 1, 33–36. https://ajindex.com/articles/267963

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