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Thyroid and Parathyroid

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thyroidectomy is about 1 percent. Differentiation of the residual thyroid cancer to<br />

. anaplastic carcinoma occurs in about 1 percent of patients <strong>and</strong> is almost always fatal<br />

Total thyroidectomy, by removing all residual normal thyroid tissue, facilitates the<br />

uptake of radioactive 131I extrinsic to the gl<strong>and</strong> <strong>and</strong> helps identify <strong>and</strong> ablate<br />

metastatic thyroid cancer. Once all thyroid tissue has been removed, thyroglobulin<br />

levels should remain below 3 ng/mL; by monitoring thyroglobulin levels, disease<br />

progress can be followed. When thyroglobulin levels increase, recurrent disease must<br />

. be present <strong>and</strong> appropriate screening with 131I should be done<br />

The patient with a thyroid nodule that is suspected to be papillary thyroid cancer<br />

should have FNAC performed. When papillary thyroid cancer is diagnosed, the<br />

definitive operation can be done without confirming the diagnosis on histologic<br />

examination. Patients with a nodule that might be papillary cancer should be treated<br />

by thyroid lobectomy, isthmectomy, <strong>and</strong> removal of any pyramidal lobe or adjacent<br />

lymph nodes. When intraoperative frozen-section examination of a lymph node or of<br />

the primary tumor confirms carcinoma, completion total or near-total thyroidectomy<br />

should be performed. If a definitive diagnosis cannot be made, the operation is<br />

terminated. When final histology confirms carcinoma, completion total thyroidectomy<br />

usually should be performed. For patients who have minimal papillary thyroid cancers<br />

confined to the thyroid gl<strong>and</strong> without angioinvasion, no further operative treatment is<br />

recommended. Treatment with thyroid hormone to suppress TSH is recommended.<br />

Patients at low risk should have serum TSH levels between 0.1 <strong>and</strong> 1.0 mU/mL,<br />

whereas patients at high risk should have serum TSH levels suppressed to less than<br />

. 0.1 mU/mL<br />

Local recurrence is a serious complication, with a disease-related mortality rate of 33<br />

to 50 percent. Patients with nodal recurrence usually do better than those with tumor<br />

recurrence in the thyroid bed or with distant metastases. Lymph node metastases in<br />

the lateral neck in patients with papillary carcinoma usually should be managed with<br />

modified radical neck dissection, <strong>and</strong> en-bloc dissection of all fibrofatty tissue <strong>and</strong><br />

lymphatic tissue. The jugular lymph node chain is removed, while preserving the<br />

sternocleidomastoid muscle, the internal jugular vein, <strong>and</strong> the spinal accessory nerve<br />

(which are all taken in a radical dissection). Dissection of the posterior triangle <strong>and</strong><br />

suprahyoid dissection usually are not necessary but should be performed when<br />

appropriate. Prophylactic neck node dissection is not necessary in patients with<br />

papillary thyroid cancer, because micrometastases appear to be ablated with<br />

radioiodine therapy. Survival rates for the different treatment modalities are<br />

. summarized in Fig. 36-26<br />

Follicular Carcinoma<br />

Follicular carcinoma, which accounts for about 10 percent of thyroid malignancies, is<br />

decreasing in incidence in the United States. This cancer occurs more often in women,<br />

with a female-to-male ratio of 3:1, <strong>and</strong> it presents in an older age group, mean age at<br />

presentation of 50 years, compared to a mean age of 35 in patients with papillary<br />

carcinoma. Follicular carcinoma occurs more frequently in iodine-deficient areas, <strong>and</strong><br />

. a rare form of familial disease is reported in patients with dyshormonogenesis<br />

Pathology

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