Sclerosing Stromal Tumor of Ovary: A Case Report

Rana, Resham Bahadur; Kafle, Santosh Upadhyaya; Jha, K. K.; Singh, Mrinalini; Gautam, Parul

doi:10.3126/bjhs.v1i1.17107

Birat J. Health Sci.

2017

DOI: 10.3126/bjhs.v1i1.17107

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Sclerosing Stromal Tumor of Ovary: A Case Report

Resham Bahadur Rana

Santosh Upadhyaya Kafle

K. K. Jha

et al.

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Cited by 2 publications

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Ovarian sclerosing stromal tumour in a 39-year-old lady- A case report and review of the literature

Thomas

Thomas²,

Mathews³

et al. 2022

IJPO

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One of the rarest ovarian sex cord-stromal tumour is Sclerosing Stromal Tumour (SST). It commonly presents as lower abdominal pain and tenderness, with or without a mass, and/or abnormal menses. As the clinical presentation and imaging are like borderline or malignant epithelial tumours and sex cord-stromal tumours, accurate preoperative clinical diagnosis can be a challenge and the diagnosis is usually made following postoperative histopathologic examination. Understanding the clinicopathological characteristics of this tumour is vital for accurate preoperative diagnosis, which can be essential for planning of care and treatment for patients. Along with a review of the current literature, we present a case of a young female with SST. This patient presented with prolonged menstrual bleeding. She underwent total abdominal hysterectomy with right salpingo-oophorectomy and left salpingectomy. The histopathological examination revealed the salient features of SST like cellular heterogeneity, hemangiopericytoma (HPC) like vascular structures, and a pseudo lobular architecture with cellular nodules separated by hypocellular, oedematous, and collagenous stroma, hence confirming the diagnosis. This case highlights the importance of considering SST as a differential diagnosis, in young patients with ovarian mass having the morphological and histopathological characteristics, despite its rarity in occurrence.

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Ovarian sclerosing stromal tumour in a 39-year-old lady- A case report and review of the literature

Thomas

Thomas²,

Mathews³

et al. 2022

IJPO

View full text Add to dashboard Cite

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Overin nadir tümörü: Sklerozan stromal tümör; 7 olgu sunumu ve literatürün gözden geçirilmesi

AYAZ

SAYHAN

KARADENİZ

et al. 2023

Dokuz Eylül Üniversitesi Tıp Fakültesi Dergisi

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Sklerozan stromal tümörler (STT), genellikle yaşamın 2-3. dekadında genç kadınlarda görülen nadir benign over tümörleridir. Over stromal tümörlerinin %2-6’sını oluştururlar. Çalışmamızda, İzmir Tepecik Eğitim ve Araştırma hastanesi patoloji bölümünde 2011-2020 yılları arasında tanı alan 7 sklerozan stromal tümör olgusunu, klinik ve histopatolojik bulgularını tekrar gözden geçirerek literatür eşliğinde sunduk . Hastalarımızın yaş ortalaması 34.4 olup 2 hasta postmenopozal dönemdeydi. Olguların 4’ünün klinik takibi mevcut olup 1 hastada operasyondan 7 yıl sonra nüks görüldü. Makroskopik olarak tümörlerin çoğu tamamıyla solid görünümdeydi. Mikroskopik olarak tüm olgularda ödemli ve /veya kollojenden zengin hiposellüler alanlarla ayrılan hipersellüler alanlardan oluşan psödolobüler düzenlenim mevcuttu. Tümör, iğsi şekilli hücreler ve bol berrak – eozinofilik şekilli yuvarlak hücrelerden oluşuyordu. Çok nadir görülmeleri nedeniyle SST de preoperatif tanı mümkün değildir. Özellikle frozen çalışılan olgularda tipik histopatolojik bulgularla doğru tanı konulması, genç kadın hastalarda fertilite koruyucu cerrahinin uygulanabilmesi açısından önem taşır.

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Sclerosing Stromal Tumor of Ovary: A Case Report

Cited by 2 publications

References 8 publications

Ovarian sclerosing stromal tumour in a 39-year-old lady- A case report and review of the literature

Ovarian sclerosing stromal tumour in a 39-year-old lady- A case report and review of the literature

Overin nadir tümörü: Sklerozan stromal tümör; 7 olgu sunumu ve literatürün gözden geçirilmesi

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