# Ancient Schwannoma of the Submandibular Gland in a Patient With Acromegaly: A Case Report

**Authors:** Zerrin Ozergin Coskun, Muhammed Sadikzade, Recep Bedir

PMC · DOI: 10.7759/cureus.98167 · Cureus · 2025-11-30

## TL;DR

A rare case of ancient schwannoma in the submandibular gland is reported in a young patient with acromegaly.

## Contribution

This is the first documented case of ancient schwannoma coexisting with acromegaly.

## Key findings

- Ancient schwannoma was confirmed histopathologically with S-100 positivity and low Ki-67 index.
- The tumor had cystic degeneration and calcifications typical of ancient schwannoma.
- No recurrence was observed at six-month follow-up after surgical excision.

## Abstract

Ancient schwannoma is a rare degenerative variant of schwannoma. Its occurrence in the submandibular gland is exceptionally uncommon, and, to the best of our knowledge, its coexistence with acromegaly has not been previously documented. A 22-year-old male patient with a history of acromegaly presented with a long-standing, painless swelling in the left submandibular region. Magnetic resonance imaging (MRI) revealed a well-defined, heterogeneous T2-hyperintense lesion with cystic and calcific components within the left submandibular gland. The patient underwent complete surgical excision of the affected gland. Histopathological examination demonstrated a spindle-cell neoplasm with nuclear palisading, cystic degeneration, and dystrophic calcifications, consistent with ancient schwannoma. Immunohistochemistry showed diffuse, strong S-100 protein positivity and a low Ki-67 proliferation index (2-3%), confirming the benign nature of the tumor. This case describes a rare coexistence of a submandibular ancient schwannoma and acromegaly in a young patient. Although a causal relationship between excess growth hormone (GH) or insulin-like growth factor 1 (IGF-1) and schwannoma development cannot be established from a single case, this association is hypothesis-generating and highlights the need for careful head and neck evaluation in patients with endocrine disorders. The patient had an uneventful postoperative course, and no recurrence was observed at six-month follow-up.

## Linked entities

- **Diseases:** acromegaly (MONDO:0019933)

## Full-text entities

- **Genes:** IGF1 (insulin like growth factor 1) [NCBI Gene 3479] {aka IGF, IGF-I, IGFI, MGF}, S100A1 (S100 calcium binding protein A1) [NCBI Gene 6271] {aka S100, S100-alpha, S100A}, GH1 (growth hormone 1) [NCBI Gene 2688] {aka GH, GH-N, GHB5, GHN, IGHD1A, IGHD1B}
- **Diseases:** submandibular ancient (MESH:D013364), Ancient Schwannoma (MESH:D009442), swelling (MESH:D004487), Acromegaly (MESH:D000172), endocrine disorders (MESH:D004700), neoplasm (MESH:D009369)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

10 references — full list in the complete paper: https://tomesphere.com/paper/PMC12754809/full.md

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Source: https://tomesphere.com/paper/PMC12754809