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Spontaneous Murine Model of Anaplastic Thyroid Cancer

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Published on: February 3, 2023

[Thymic basaloid carcinoma].

Yoshihiko Tsunoda¹, Koichi Tanaka, Kuniaki Okada

¹Department of Surgery, Sapporo-Kosei General Hospital, Sapporo, Japan.

Kyobu Geka. the Japanese Journal of Thoracic Surgery

|September 18, 2010

Summary

A rare thymic basaloid carcinoma, often linked with multilocular thymic cysts, was successfully resected in a 72-year-old male. This case highlights the importance of careful follow-up for this low-grade malignancy.

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Derivation of Thymic Lymphoma T-cell Lines from Atm-/- and p53-/- Mice

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Published on: April 3, 2011

Area of Science:

Thoracic oncology
Pathology
Surgical oncology

Context:

Anterior mediastinal solid tumors are rare, with thymic basaloid carcinoma being an exceptionally uncommon subtype.
This specific case involved a 72-year-old male with a growing anterior mediastinal tumor incidentally found during lung follow-up.
The tumor was associated with a multilocular thymic cyst, a known co-occurrence with thymic basaloid carcinoma.

Purpose:

To report a rare case of thymic basaloid carcinoma.
To discuss the diagnostic and treatment approach for this rare thymic neoplasm.
To emphasize the association between thymic basaloid carcinoma and multilocular thymic cysts.

Summary:

A 72-year-old male presented with an anterior mediastinal solid tumor, diagnosed as thymic basaloid carcinoma post-thymectomy.
Histopathological analysis confirmed thymic basaloid carcinoma, a rare entity often associated with multilocular thymic cysts.
The patient underwent radical thymectomy, with no recurrence observed at 12 months post-operation.

Impact:

This case contributes to the limited international literature on thymic basaloid carcinoma, with only 32 cases previously reported.
Surgical resection is confirmed as the primary treatment modality.
Highlights the need for vigilant post-operative surveillance due to potential for recurrence and mortality, despite its generally low-grade nature.