An ectopic hamartomatous thymoma compressing left jugular vein.
@article{Huang2014AnEH,
title={An ectopic hamartomatous thymoma compressing left jugular vein.},
author={L Huang and L. Zhao and Y Chai},
journal={Nigerian journal of clinical practice},
year={2014},
volume={17 6},
pages={
814-6
}
}Ectopic hamartomatous thymoma (EHT) is an extremely rare benign neoplasm. It is usually found at the root of the neck (frequently on the left) and does not usually impact adjacent tissues in clinically significant ways. While EHT manifests distinct pathological features, the lesion is either asymptomatic or may show nonspecific clinical features. We report one case of EHT which was assumed to be of low malignant potential since it severely compressed the inlet of left internal jugular vein as…
4 Citations
Ectopic hamartomatous thymoma (biphenotypic branchioma)
- MedicineMedicine
- 2018
The patient had no evidence of metastasis or recurrence for 26 months after the operation and it can be considered to update the name to “biphenotypic branchioma” in order to avoid conceptual confusion.
Ectopic hamartomatous thymoma: report of a case and review of literature.
- MedicineInternational journal of clinical and experimental pathology
- 2015
The clinicopathological features of a case of EHT in a 28-year-old Chinese male, together with a literature review, show a 3.0-cm well-defined nodule of heterogeneous density located within the left sternocleidomastoid muscle.
Ectopic Hamartomatous Thymoma: A Review Of The Literature With Report Of New Cases And Proposal Of A New Name: Biphenotypic Branchioma
- MedicineHead and Neck Pathology
- 2017
As this entity is a neoplasm that shows dual mesoderm and endoderm derivation/differentiation, a new name “biphenotypic branchioma” is proposed, to avoid taxonomic confusion, international consensus on terminology is desired.
A case report and review of the literature
- Medicine
- 2017
A 4-month-old female presented with severe jaundice, pruritus, and pale stool for 20 days and was diagnosed with BA combined with PFIC3, a disease that leads to intrahepatic cholestasis.
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