Sex cord tumor with annular tubules

Sex cord tumor with annular tubules is a rare type of ovarian tumor, which seems to arise from Sertoli cells. Most tumors are associated with Peutz<i>-</i>Jeghers syndrome and have a benign course and favorable prognosis; however, about 20% of sporadic sex cord tumors with annular tubules have a high risk of developing metastases. We present a case report about 18-year-old patient who presented with irregular menstruation and abdominal pain. Based on the histological features and immunohistochemical results, the diagnosis of a sex cord tumor with annular tubules was confirmed. The above-described ovarian tumor is rare in childhood and adolescence compared to the general population, which, combined with nonspecific clinical manifestations, can result certain diagnostic difficulties in this age group of patients.

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Publication Details

Journal
Russian Journal of Archive of Pathology
Published
2025-02-12
DOI
https://doi.org/10.17116/patol20258701148
Primary Topic
Genetic factors in colorectal cancer
Type
article
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article

Sex cord tumor with annular tubules

Бадлаева Алина Станиславовна, V. V. Sukhoparova, А. П. Ракша, A.V. Asaturova et al.
Russian Journal of Archive of Pathology
Genetic factors in colorectal cancer
article

Sex cord tumor with annular tubules

Бадлаева Алина Станиславовна, V. V. Sukhoparova, А. П. Ракша, A.V. Asaturova, Anna Tregubova, N. L. Lysova, R.B. Matronitskii
article en

Abstract

Sex cord tumor with annular tubules is a rare type of ovarian tumor, which seems to arise from Sertoli cells. Most tumors are associated with Peutz<i>-</i>Jeghers syndrome and have a benign course and favorable prognosis; however, about 20% of sporadic sex cord tumors with annular tubules have a high risk of developing metastases. We present a case report about 18-year-old patient who presented with irregular menstruation and abdominal pain. Based on the histological features and immunohistochemical results, the diagnosis of a sex cord tumor with annular tubules was confirmed. The above-described ovarian tumor is rare in childhood and adolescence compared to the general population, which, combined with nonspecific clinical manifestations, can result certain diagnostic difficulties in this age group of patients.

Russian Journal of Archive of PathologyVol. 87(1)
Pirogov Russian National Research Medical University (RU), National Medical Research Center for Obstetrics, Gynecology and Perinatology named after Academician V.I.Kulakov of the Ministry of Healthcare of the Russian Federation (RU)
Good health and well-being
Openalex Percentile: Top 96%
Genetic factors in colorectal cancer
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Sex cord tumor with annular tubules — Бадлаева Алина Станиславовна, V. V. Sukhoparova, et al. · Russian Journal of Archive of Pathology (2025) | TGRS Research Map | TGRS