FAMILIAL SYNDROMIC PAPILLARY THYROID CARCINOMA - REPORT OF TWO CASES

Papillary thyroid cancer types

Background: Thyroid nodules were reported with high prevalence in acromegalic patients.

papillary thyroid cancer types

Patients and methods: 63 acromegalic patients 16 males and 47 femalesaged at diagnosis Median duration of acromegaly was 8 years.

Thyroid ultrasound was performed.

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In suspected nodules, pathological examination either fine needle aspiration with cytology exam or pathology exam after thyroidectomy was papillary thyroid cancer types.

Results: Median thyroid volume was Thyroid nodules were present in 52 patients Multiple thyroid nodules were found in 45 out of 52 cases Toxic multinodular goiter was prezent in 5 patients 7. Average maximum diameter of dominant nodule was 1.

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Thyroid differentiated cancer was diagnosed in 6 patients 9. Histological type was papillary carcinoma: 3 macrocarcinomas and 3 microcarcinomas follicular variant of papillary carcinomas ; two microcarcinomas were multifocal.

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Five patients with thyroid carcinomas underwent thyroidectomy; 4 patients two macrocarcinomas and two multifocal microcarcinomas also received radioiodine treatment. Thyroid surgery is pending in one patient.

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Autoimmune thyroiditis was present in 4 patients 6. Conclusion: Multinodular nontoxic thyroid disease was vermox oxiuri frequent in our series of acromegalic patients.

papillary thyroid cancer types

We also found an increased prevalence of differentiated thyroid carcinoma. Careful clinical thyroid examination, thyroid ultrasound and cytological exam were recommended in acromegalic patients. This Volume.

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