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Updated: Jul 25, 2026

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An Orthotopic Mouse Model of Anaplastic Thyroid Carcinoma
Published on: April 17, 2013
[Epithelioid hemangiosarcoma of the thyroid gland]
Casopis Lekaru Ceskych
|June 14, 2002
Summary
This case report details an aggressive epithelioid hemangiosarcoma of the thyroid gland in a 54-year-old female. The rare thyroid cancer showed unusual metastasis and was fatal within three months.
Area of Science:
- Oncology
- Pathology
- Endocrinology
Background:
- Epithelioid hemangiosarcoma is a rare vascular tumor.
- Thyroid gland tumors are uncommon, with epithelioid hemangiosarcoma being exceptionally rare.
- Eufunctional nodular goiter is a common thyroid condition.
Observation:
- A 54-year-old female with a history of eufunctional nodular goiter presented with epithelioid hemangiosarcoma of the thyroid.
- The tumor exhibited highly aggressive behavior with early generalization.
- Unusual metastatic spread to the stomach and duodenum walls was observed.
Findings:
- The patient underwent total thyroidectomy, cervical lymph node dissection, and chemotherapy.
- Despite aggressive treatment, the tumor demonstrated rapid progression and dissemination.
- Therapeutically unmanageable gastrointestinal bleeding led to the patient's death three months post-surgery.
Implications:
- This case highlights the aggressive nature and unusual metastatic patterns of thyroid epithelioid hemangiosarcoma.
- It underscores the importance of considering rare malignancies in thyroid pathology.
- Further research into the pathogenesis and treatment of this rare tumor is warranted.
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