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Thyroid spindle epithelial tumor with thymus-like differentiation (SETTLE): case report and review
Luiz Antônio Magnata Filho1, Maria Alice Neves Bordallo, Cencita H C N Pessoa
1Department of Pediatric Endocrinology, Instituto Nacional de Câncer, Rio de Janeiro, RJ, Brazil.
Spindle epithelial tumor with thymus-like element (SETTLE) is a rare pediatric thyroid cancer. This report details a unique case in Brazil, highlighting its biphasic pattern and successful surgical outcome with no recurrence after five years.
Area of Science:
- Endocrinology and Oncology
- Pediatric Pathology
- Surgical Oncology
Background:
- Spindle epithelial tumor with thymus-like element (SETTLE) is an exceptionally rare malignant thyroid neoplasm.
- Predominantly affects pediatric and young adult populations, typically presenting as a localized thyroid mass.
- Origin is hypothesized to involve branchial pouch or thymic remnant tissue with primitive thymic differentiation.
Observation:
- A clinical, cytological, histological, and immunohistochemical analysis of a SETTLE case in a 3-year-old girl is presented.
- Microscopic examination revealed a biphasic neoplasm characterized by a prominent spindle cell component and a minor glandular component.
- The glandular component exhibited mucinous or respiratory-type epithelium.
Findings:
- Immunohistochemical analysis demonstrated strong and diffuse positivity for pan-cytokeratin (pan-CK), vimentin, and smooth muscle actin.
- This case represents the first reported instance of SETTLE in Brazil.
- The patient remained disease-free, with no evidence of recurrence or metastasis five years post-surgery.
Implications:
- This report expands the geographic and clinical understanding of SETTLE.
- The findings underscore the importance of comprehensive histopathological and immunohistochemical evaluation for diagnosing rare pediatric thyroid tumors.
- The favorable long-term outcome in this case suggests that complete surgical resection may be an effective treatment strategy for SETTLE.
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