# Uterine Leiomyosarcoma in a 22-Year-Old Young Woman: A Case Report

**Authors:** Mohammed Bendimya, Fatima Rezzoug, Mouhsine Omari, Ouissam Al Jarroudi, Sami Aziz Brahmi, Said Afqir

PMC · DOI: 10.7759/cureus.62087 · Cureus · 2024-06-10

## TL;DR

This paper reports a rare case of uterine leiomyosarcoma in a young 22-year-old woman, highlighting the challenges in diagnosis and treatment.

## Contribution

The novelty lies in presenting a rare case of uterine leiomyosarcoma in a very young patient, emphasizing the importance of histopathological confirmation.

## Key findings

- Uterine leiomyosarcoma was diagnosed in a 22-year-old woman following surgery and histopathological analysis.
- The case highlights the poor prognosis and high recurrence rate of this rare gynecological cancer.
- Surgical intervention remains the primary treatment for localized leiomyosarcoma.

## Abstract

Leiomyosarcoma is one of the rarest types of gynecological cancer. It is a relatively rare condition that affects young women. The most frequent symptom of this disease is vaginal bleeding. The primary treatment for localized disease is still surgical intervention. It is widely recognized that leiomyosarcoma has a poor prognosis, with reduced survival rates and a high likelihood of early recurrence. This report presents a case of uterine leiomyosarcoma in a 22-year-old female patient. Following a total hysterectomy and bilateral salpingo-oophorectomy, the diagnosis of leiomyosarcoma was confirmed through a histopathological examination of the surgical specimen.

## Linked entities

- **Diseases:** Leiomyosarcoma (MONDO:0005058), uterine leiomyosarcoma (MONDO:0016262)

## Full-text entities

- **Diseases:** gynecological cancer (MESH:D009369), vaginal bleeding (MESH:D014592), Leiomyosarcoma (MESH:D007890)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11236299/full.md

## References

49 references — full list in the complete paper: https://tomesphere.com/paper/PMC11236299/full.md

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Source: https://tomesphere.com/paper/PMC11236299