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Peer-reviewedCC BY 4.0Clinical Case Reports

Pararectal Leiomyosarcoma Following Total Laparoscopic Hysterectomy (TLH) for Initially Diagnosed Uterine Leiomyoma

  • Nanna Monjé1
  • Matthias Alexa1
  • Annette Hasenburg1
  • Yaman Degirmenci1
  1. 1Department of Gynecology and Obstetrics University Medical Center of the Johannes Gutenberg University Mainz Germany
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Abstract

This case report highlights the diagnostic challenges of clinically distinguishing leiomyomas and leiomyosarcomas and the importance of post‐hysterectomy monitoring. Patients with extensive prior oncological treatments and genetic cancer predisposition require individualized surveillance strategies, as they remain at elevated risk for secondary malignancies that may present in unusual locations or timeframes.

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Cite

BibTeXRIS
BibTeX
@article{monje2026pararectal,
  title = {{Pararectal Leiomyosarcoma Following Total Laparoscopic Hysterectomy (TLH) for Initially Diagnosed Uterine Leiomyoma}},
  author = {Nanna Monjé and Matthias Alexa and Annette Hasenburg and Yaman Degirmenci},
  journal = {Clinical Case Reports},
  year = {2026},
  month = nov,
  doi = {10.1002/ccr3.73090},
  url = {https://doi.org/10.1002/ccr3.73090},
  note = {CC BY 4.0},
}
RIS
TY  - JOUR
TI  - Pararectal Leiomyosarcoma Following Total Laparoscopic Hysterectomy (TLH) for Initially Diagnosed Uterine Leiomyoma
AU  - Nanna Monjé
AU  - Matthias Alexa
AU  - Annette Hasenburg
AU  - Yaman Degirmenci
PY  - 2026
DA  - 2026/11/04
JO  - Clinical Case Reports
DO  - 10.1002/ccr3.73090
UR  - https://doi.org/10.1002/ccr3.73090
AB  - This case report highlights the diagnostic challenges of clinically distinguishing leiomyomas and leiomyosarcomas and the importance of post‐hysterectomy monitoring. Patients with extensive prior oncological treatments and genetic cancer predisposition require individualized surveillance strategies, as they remain at elevated risk for secondary malignancies that may present in unusual locations or timeframes.
SN  - 2050-0904
ER  -