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SOLITARY METASTASIS OF RENAL CLEAR CELL CARCINOMA TO HÜRTHLE CELL ADENOMA OF THYROID GLAND: REPORT OF A CASE RITA PASSANTINO - LORENZO MARASA’ Department of Pathology, A.R.N.A.S. Civico, Palermo RITA PASSANTINO - LORENZO MARASA’ Department of Pathology, A.R.N.A.S. Civico, Palermo
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INTRODUCTIONINTRODUCTION Metastases to the thyroid gland are a common finding at autopsy in patients who died of malignancy and are often misdiagnosed as primary thyroid neoplasms clinically. Metastatic Renal Cell Carcinoma (RCC) to the thyroid gland is a rare occurence but must be considered in the differential diagnosis of Clear Cell Tumours (CCT) of the thyroid gland to prevent misclassification, potentially resulting in inappropriate clinical management. We present a patient with a rare, unusual case of RCC metastatic to a Hürthle cell adenoma of the thyroid gland. Metastases to the thyroid gland are a common finding at autopsy in patients who died of malignancy and are often misdiagnosed as primary thyroid neoplasms clinically. Metastatic Renal Cell Carcinoma (RCC) to the thyroid gland is a rare occurence but must be considered in the differential diagnosis of Clear Cell Tumours (CCT) of the thyroid gland to prevent misclassification, potentially resulting in inappropriate clinical management. We present a patient with a rare, unusual case of RCC metastatic to a Hürthle cell adenoma of the thyroid gland.
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CASE REPORT The patient was a 77-year-old sicilian woman who was referred to our department after a thyroid tumour was identified in February 2008. She had a history of RCC of the left kidney, which had been resected 3 years previously. Ultrasound sonography demonstrated a well- demarcated hypoechoic mass which measured 3.5 cm in greatest diameter and occupied the left lobe. A total thyroidectomy was performed on March 2008. A solitary, well circumscribed, encapsulated, bright yellow to reddish-tan mass with hemorrhage and degenerative changes, which measured 3.5 cm in greatest diameter and occupied the left lobe of the thyroid gland. The patient was a 77-year-old sicilian woman who was referred to our department after a thyroid tumour was identified in February 2008. She had a history of RCC of the left kidney, which had been resected 3 years previously. Ultrasound sonography demonstrated a well- demarcated hypoechoic mass which measured 3.5 cm in greatest diameter and occupied the left lobe. A total thyroidectomy was performed on March 2008. A solitary, well circumscribed, encapsulated, bright yellow to reddish-tan mass with hemorrhage and degenerative changes, which measured 3.5 cm in greatest diameter and occupied the left lobe of the thyroid gland.
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HISTOLOGICAL EXAMINATION A Hürthle cell adenoma containing large clusters of cells with abundant clear cytoplasm and round nuclei. The predominant histologic pattern was characterized by the presence of small nests, cords and “pseudofollicles” made up of neoplastic cells separated by a prominent vascular stroma with sinusoidal-type blood vessels and intraluminal fresh hemorrhage. Metastatic cells contained variable amounts of PAS- positive material which was indicative of glycogen in the cytoplasm of the clear cells. Metastasis showed morphological characteristics identical to the RCC resected 3 years previously. A Hürthle cell adenoma containing large clusters of cells with abundant clear cytoplasm and round nuclei. The predominant histologic pattern was characterized by the presence of small nests, cords and “pseudofollicles” made up of neoplastic cells separated by a prominent vascular stroma with sinusoidal-type blood vessels and intraluminal fresh hemorrhage. Metastatic cells contained variable amounts of PAS- positive material which was indicative of glycogen in the cytoplasm of the clear cells. Metastasis showed morphological characteristics identical to the RCC resected 3 years previously.
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IMMUNOHISTOCHEMICAL EXAMINATION Specific markers of Hürthle cell adenoma such as thyroglobulin, CK14, CEA, S-100 protein and HMB-45 stained negatively in the clear neoplastic cells. Specific markers of RCC such as EMA and vimentin stained positively. Specific markers of Hürthle cell adenoma such as thyroglobulin, CK14, CEA, S-100 protein and HMB-45 stained negatively in the clear neoplastic cells. Specific markers of RCC such as EMA and vimentin stained positively. THYROGLOBULIN VIMENTIN EMA
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CONCLUSIONSCONCLUSIONS The thyroid gland is a rare site of tumour metastasis. RCC is one of the more common neoplasm to metastasize to the thyroid gland (<0.1%). Metastatic RCC to a thyroid neoplasm is extremely rare, with only three reports found in the international literature. The possibility of metastatic RCC should always be taken under consideration, especially when nests of clear cells are seen infiltrating into the thyroid parenchyma or neoplasm. The thyroid gland is a rare site of tumour metastasis. RCC is one of the more common neoplasm to metastasize to the thyroid gland (<0.1%). Metastatic RCC to a thyroid neoplasm is extremely rare, with only three reports found in the international literature. The possibility of metastatic RCC should always be taken under consideration, especially when nests of clear cells are seen infiltrating into the thyroid parenchyma or neoplasm.
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CONCLUSIONSCONCLUSIONS Our report shows that the architectural, cytologic, hi- stologic, histochemical, and immunohistochemical fea- tures are sufficiently distinctive to allow differentation of a primary thyroid epithelial neoplasm with clear cell changes from metastatic RCC. This distinction is important to correctly manage the patient. Surgical treatment is recommended as the patient may enjoy a prolonged survival. MAIN REFERENCE: Qian L. Renal cell carcinoma metastatic to Hürthle cell adenoma of thyroid. Ann Diagn Pathol. 2004 Oct; 8(5): 305-8. Qian L. Renal cell carcinoma metastatic to Hürthle cell adenoma of thyroid. Ann Diagn Pathol. 2004 Oct; 8(5): 305-8. Our report shows that the architectural, cytologic, hi- stologic, histochemical, and immunohistochemical fea- tures are sufficiently distinctive to allow differentation of a primary thyroid epithelial neoplasm with clear cell changes from metastatic RCC. This distinction is important to correctly manage the patient. Surgical treatment is recommended as the patient may enjoy a prolonged survival. MAIN REFERENCE: Qian L. Renal cell carcinoma metastatic to Hürthle cell adenoma of thyroid. Ann Diagn Pathol. 2004 Oct; 8(5): 305-8. Qian L. Renal cell carcinoma metastatic to Hürthle cell adenoma of thyroid. Ann Diagn Pathol. 2004 Oct; 8(5): 305-8.
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