# Case Report: The leiomyoma-leiomyosarcoma sequence exists in the esophagus: first case of malignant transformation treated with endoscopic submucosal dissection

**Authors:** Xu Wang, Gen Gui, Ruixue Liu, Zhaoyun Yang, Guifang Xu, Bin Sun

PMC · DOI: 10.3389/fmed.2025.1716368 · Frontiers in Medicine · 2026-01-12

## TL;DR

This case report describes the first known instance of a benign esophageal tumor turning malignant and successfully treated with a minimally invasive procedure.

## Contribution

The first documented case of malignant transformation from esophageal leiomyoma to leiomyosarcoma treated via endoscopic submucosal dissection.

## Key findings

- A 0.8 cm esophageal submucosal nodule was resected and found to contain both benign and malignant tissue.
- The malignant region showed high cellularity, nuclear atypia, increased mitotic activity, and loss of smooth muscle markers.
- The patient had no recurrence at 60-day follow-up after complete resection with tumor-free surgical margins.

## Abstract

Esophageal leiomyosarcoma (ELMS) is an extremely rare malignant tumor, and the possibility of malignant transformation from benign esophageal leiomyoma has historically been dismissed. This report presents, to our knowledge, the first documented case of malignant transformation within an esophageal leiomyoma and its successful treatment via endoscopic submucosal dissection (ESD), challenging the conventional belief regarding the absolute benignity of esophageal leiomyomas.

A 52-year-old female presented with non-specific symptoms and was found to have a small (0.8 cm) esophageal submucosal nodule during gastroscopy. Endoscopic ultrasound (EUS) showed a well-defined hypoechoic lesion originating from the submucosal layer. The lesion was completely resected via ESD. Histopathological examination demonstrated a conventional leiomyoma with a focal area of malignant transformation to leiomyosarcoma, characterized by high cellularity, nuclear atypia, increased mitotic activity [5 per 2 high-power fields (HPF)], elevated Ki-67 index (40%), and loss of smooth muscle markers (SMA, desmin) in the malignant region. Surgical margins were tumor-free. The patient recovered well with no recurrence at 60-day follow-up.

## Linked entities

- **Proteins:** SMN1 (survival of motor neuron 1, telomeric), LOC101066771 (desmin-like), Mki67 (antigen identified by monoclonal antibody Ki 67)
- **Diseases:** leiomyoma (MONDO:0001572), leiomyosarcoma (MONDO:0005058), esophageal leiomyosarcoma (MONDO:0003365)

## Full-text entities

- **Genes:** SMN1 (survival of motor neuron 1, telomeric) [NCBI Gene 6606] {aka BCD541, GEMIN1, SMA, SMA1, SMA2, SMA3}, DES (desmin) [NCBI Gene 1674] {aka CDCD3, CSM1, CSM2, LGMD1D, LGMD1E, LGMD2R}
- **Diseases:** ELMS (MESH:D007890), tumor (MESH:D009369), esophageal leiomyoma (MESH:D007889)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12833043/full.md

## References

22 references — full list in the complete paper: https://tomesphere.com/paper/PMC12833043/full.md

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Source: https://tomesphere.com/paper/PMC12833043