# Ectopic Cervical Thymoma with Myasthenia Gravis and Pure Red Cell Aplasia: A Case Report

**Authors:** Eiji Narusawa, Kai Obayashi, Sayaka Obayashi, Toshiteru Nagashima, Natsuko Kawatani, Tomohiro Yazawa, Ryohei Yoshikawa, Nozomi Matsumura, Ken Shirabe, Seshiru Nakazawa

PMC · DOI: 10.70352/scrj.cr.25-0818 · Surgical Case Reports · 2026-03-27

## TL;DR

A rare case of ectopic cervical thymoma linked to myasthenia gravis and pure red cell aplasia is reported, with successful surgical treatment.

## Contribution

This case report presents a rare combination of ectopic cervical thymoma with myasthenia gravis and pure red cell aplasia.

## Key findings

- The patient had an ectopic cervical thymoma (type AB) and an occult type A thymoma in the thymus.
- Surgical removal of the cervical mass and extended thymectomy led to an uneventful recovery.
- The case highlights the importance of considering ectopic thymomas in patients with myasthenia gravis.

## Abstract

Ectopic cervical thymoma is an extremely rare tumor, particularly when associated with myasthenia gravis and pure red cell aplasia.

A 65-year-old female was undergoing treatment for myasthenia gravis and pure red cell aplasia at our hospital. Myasthenia gravis symptoms were controlled with prednisolone, and aplasia was managed using oral cyclosporine A. A gradually increasing cervical mass had been noted previously. Needle biopsy of the mass suggested an ectopic thymoma, and the patient was referred for surgery. Preoperative chest CT revealed a 6.5-cm solid mass within the caudal portion of the left thyroid lobe, which was displacing the trachea to the right. No continuity was noted between the cervical lesion and the thymus. Fluorodeoxyglucose PET showed fluorodeoxyglucose uptake in the mass, with a maximum standardized uptake value of 6.48. No other abnormal uptake was observed, including that in the thymus. The preoperative diagnosis was an intrathyroidal ectopic cervical thymoma associated with myasthenia gravis and pure red cell aplasia. Based on the history of myasthenia gravis, both extended thymectomy and left thyroid lobectomy were performed. The postoperative course was uneventful. Histopathological examination showed that the cervical mass was a type AB thymoma. The examination also revealed an occult type A thymoma (Masaoka stage II) in the thymus.

We encountered a rare case of type AB ectopic cervical thymoma associated with myasthenia gravis and pure red cell aplasia. Extended thymectomy and cervical tumor resection revealed the presence of an occult type A thymoma in the thymus.

## Linked entities

- **Chemicals:** prednisolone (PubChem CID 5755), cyclosporine A (PubChem CID 5284373), fluorodeoxyglucose (PubChem CID 53716604)
- **Diseases:** myasthenia gravis (MONDO:0009688), pure red cell aplasia (MONDO:0001705)

## Full-text entities

- **Diseases:** cervical tumor (MESH:D002583), Ectopic Cervical Thymoma (MESH:D013945), aplasia (MESH:C536482), cervical lesion (MESH:D002575), tumor (MESH:D009369), Myasthenia Gravis (MESH:D009157), Pure Red Cell Aplasia (MESH:D012010), II (MESH:C537730)
- **Chemicals:** Fluorodeoxyglucose (MESH:D019788), prednisolone (MESH:D011239), cyclosporine A. (MESH:D016572)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

18 references — full list in the complete paper: https://tomesphere.com/paper/PMC13043206/full.md

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Source: https://tomesphere.com/paper/PMC13043206