# A Case of Neurofibroma in the Supraumbilical Region Undergoing Cystic Myxomatous Degeneration: An Unusual Presentation

**Authors:** Yogesh B Manek, Suhas Jajoo, Chandrashekhar Mahakalkar, Shivani Kshirsagar

PMC · DOI: 10.7759/cureus.54246 · Cureus · 2024-02-15

## TL;DR

A rare case of neurofibroma in the belly button area with unusual cystic changes is reported in a 75-year-old woman.

## Contribution

This paper presents an unusual case of neurofibroma with cystic myxomatous degeneration in a rare anatomical location.

## Key findings

- A 75-year-old female had a reddish-yellow cystic mass in the supraumbilical region.
- Histopathology confirmed neurofibroma with cystic myxomatous degeneration.
- Surgical excision and careful pathological examination were essential for diagnosis and treatment.

## Abstract

Primary umbilical neoplasms are exceptionally rare. Neurofibromas histologic findings vary from collagenous to myxoid matrix according to the neoplastic elements differentiation. We present a case of neurofibroma in the supraumbilical region undergoing cystic myxomatous degeneration. A 75-year-old female presented to the department with a complaint of swelling above the umbilicus for the last three years. The swelling was excised and grossly was a single, irregular, reddish-yellow cystic mass measuring 4.5 × 4 x 3 cm. On the cut section, cystic jelly-like areas were identified, and histopathological features were suggestive of neurofibroma undergoing cystic myxomatous degeneration. The diagnosis needed to be combined with pathological examination, and careful consideration during the surgical intervention was important to confirm there was no residue.

## Linked entities

- **Diseases:** neurofibroma (MONDO:0016755)

## Full-text entities

- **Diseases:** swelling (MESH:D004487), swelling above the umbilicus (MESH:C537059), Primary umbilical neoplasms (MESH:D014496), Neurofibroma (MESH:D009455), Cystic Myxomatous Degeneration (MESH:D018297)

## Full text

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## Figures

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## References

13 references — full list in the complete paper: https://tomesphere.com/paper/PMC10944324/full.md

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Source: https://tomesphere.com/paper/PMC10944324