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Poorly differentiated thyroid carcinoma arising from substernal goiter: a case report.
Shant Apelian1, Sawsan Ismail2, Dommar Roumieh3
1Department of Obstetrics and Gynecology, Tishreen University Hospital, Latakia, Syria.
Annals of Medicine and Surgery (2012)
|May 2, 2024
Summary
This case report details a rare poorly differentiated thyroid carcinoma originating from a substernal goiter in a 54-year-old female. The study emphasizes the diagnostic challenges and importance of histopathology for thyroid neoplasms.
Area of Science:
- Endocrinology
- Oncology
- Pathology
Background:
- Poorly differentiated thyroid carcinoma (PDTC) is a rare malignancy, comprising 2-4% of thyroid neoplasms.
- Substernal goiter (SG) is an enlarged thyroid gland extending below the thoracic inlet; malignant neoplasms arising from SG are exceptionally rare (2-3% of cases).
Observation:
- A 54-year-old female presented with dysphagia, dyspnea, cervical swelling, and anorexia.
- Radiological and clinical examinations led to total thyroidectomy with lymph node dissection.
- Microscopic examination revealed an infiltrative PDTC with insular, trabecular, and solid formations, characterized by specific cellular and nuclear features, and areas of necrosis.
Findings:
- The final diagnosis was multifocal poorly differentiated thyroid carcinoma arising from a substernal goiter.
- Histopathological features presented diagnostic challenges due to tumor heterogeneity.
- Diagnosis was confirmed using the Turin Criteria, emphasizing histopathological examination.
Implications:
- This case highlights the importance of thorough histopathological evaluation of thyroid nodules, especially in substernal goiters.
- Early and accurate diagnosis of PDTC is crucial for effective management.
- The study underscores the diagnostic complexities associated with rare thyroid malignancies.
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