Rare Diagnosis of Metastatic Papillary Thyroid Carcinoma Through Pericardial Effusion

Unveiling a Rare Case: Key Findings

  • A 54-year-old male presented with chest pain, dyspnea, and pericardial effusion.
  • Cytological analysis of pericardial fluid revealed malignant cells, leading to further investigation.
  • PET/CT scans detected mediastinal and abdominal lymphadenopathy.
  • Biopsies confirmed metastatic papillary thyroid carcinoma with “signet-ring” cell morphology.
  • The patient was referred for oncological management, ruling out surgical intervention due to advanced disease stage.

The Role of Histopathology in Diagnosis The differentiation of metastatic adenocarcinomas is crucial. The “signet-ring” cell morphology is rare in thyroid carcinomas and more commonly associated with gastric cancers. Immunohistochemical staining played a pivotal role, confirming positivity for CK7, TTF1, Thyroglobulin, and Galectin-3, leading to the diagnosis of metastatic papillary thyroid carcinoma.

Exploring the Broader Implications

  • Metastatic thyroid carcinomas can present in unusual sites like the pericardium.
  • Histopathological features, including immunostaining, aid in differential diagnosis.
  • Oncological advancements emphasize targeted therapies for such rare malignancies.

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