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Micronodular Thymic Carcinoma with Lymphoid Stroma: A Case Report.
Koki Zaitsu1, Haruto Nishida1, Yoshihiko Kondo1
1Department of Diagnostic Pathology, Faculty of Medicine, Oita University, Yufu, Japan.
International Journal of Surgical Pathology
|October 31, 2022
Summary
This case report details a rare micronodular thymic carcinoma (MTC) with lymphoid hyperplasia. The tumor showed mixed low-grade and malignant features, lacking typical favorable prognostic markers.
Area of Science:
- Oncology
- Pathology
- Genetics
Background:
- Micronodular thymic carcinoma (MTC) with lymphoid hyperplasia is considered the malignant counterpart of micronodular thymoma (MT) with lymphoid hyperplasia.
- MTC shares morphological similarities with MT, suggesting a potential malignant transformation pathway.
- This report presents a unique case of MTC with lymphoid hyperplasia.
Observation:
- A 53-year-old woman presented with an incidentally discovered chest tumor.
- Histopathological examination revealed nodular epithelial nests with malignant morphology, including atypical cells and comedo necrosis, transitioning to low-grade thymoma-like areas.
- Immunohistochemistry showed expression of GLUT1, CD5, KIT, and BCL2 in carcinomatous elements, with attenuated expression in low-grade areas.
Findings:
- The tumor was negative for the *GTF2I* point mutation and Langerhans/dendritic cells, which are typically associated with favorable thymoma prognosis.
- The patient developed pleural metastasis 27 months postoperatively, necessitating treatment with lenvatinib.
- This case represents the first reported instance of a partially low-grade, *GTF2I*-negative MTC.
Implications:
- Histological and genetic findings in MTC may serve as prognostic indicators.
- Understanding the characteristics of this *GTF2I*-negative MTC could inform future diagnostic and therapeutic strategies.
- Further research into MTC subtypes and their genetic profiles is warranted to improve patient outcomes.

