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Thyroid and Parathyroid

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Follicular carcinoma usually is solitary <strong>and</strong> approximately 90 percent are surrounded<br />

by a tumor capsule. Follicular carcinoma differs from papillary carcinoma in that<br />

vascular invasion <strong>and</strong> hematogenous spread to bone, lung, <strong>and</strong> liver is seen more<br />

commonly than lymphatic spread, which usually is encountered in late stages. Lymph<br />

node metastases occur in less than 10 percent of patients. Histologically, follicles are<br />

present, but the lumen may be devoid of colloid. Architectural patterns depend on the<br />

. degree of differentiation demonstrated by the tumor<br />

Two types of follicular carcinoma are recognized. In minimally invasive tumors there<br />

is evidence of invasion into but not through the tumor capsule at one or more spots.<br />

Previously, these tumors may have been reported as atypical adenomas, although<br />

there are reports of metastases occurring, <strong>and</strong> they should be regarded as low-grade<br />

carcinomas. In the second type, frankly invasive tumors, there is evidence of vascular<br />

invasion or tumor invasion through the tumor capsule. Tumor infiltration <strong>and</strong> invasion<br />

may be apparent at surgery, with tumor thrombus in the middle thyroid or jugular<br />

. veins<br />

Clinical Manifestations<br />

Follicular cancers usually present as solitary thyroid nodules, occasionally with a<br />

history of rapid size increase, <strong>and</strong> long-st<strong>and</strong>ing goiter. When hemorrhage into the<br />

nodule has occurred, pain may be a presenting feature, but usually the tumors are<br />

painless. At initial presentation cervical lymphadenopathy is uncommon, although<br />

distant metastases are more frequently encountered than papillary carcinoma. Rarely,<br />

follicular cancers may be hyperfunctioning (1 percent), <strong>and</strong> patients may present with<br />

. signs <strong>and</strong> symptoms of thyrotoxicosis<br />

Unless distant metastases have been confirmed as follicular thyroid cancer, definitive<br />

preoperative diagnosis usually is not possible in follicular thyroid carcinoma. This is<br />

because FNAC is unable to distinguish between follicular cells from a benign<br />

follicular adenoma <strong>and</strong> from a carcinoma. Approximately 20 percent of all FNAC<br />

aspirates showing follicular cells are carcinomas; the remaining 80 percent are<br />

. adenomas<br />

Surgical Treatment <strong>and</strong> Prognosis<br />

Patients diagnosed by FNAC as having a follicular lesion should undergo thyroid<br />

lobectomy, including the isthmus <strong>and</strong> the pyramidal lobe. Intraoperative frozensection<br />

examination usually is not helpful but should be performed when there is<br />

evidence of capsular or vascular invasion or when adjacent lymphadenopathy is<br />

present. Total thyroidectomy should be performed when thyroid cancer is diagnosed,<br />

except in patients with minimally invasive follicular cancers because the prognosis in<br />

these patients is so good. In older patients, when follicular neoplasms diagnosed by<br />

FNAC are greater than 4 cm <strong>and</strong> macroscopically suspicious for cancer, some<br />

surgeons proceed with total thyroidectomy, because the risk of cancer is about 50<br />

percent. A diagnosis of invasive carcinoma necessitates completion total<br />

thyroidectomy primarily so that 131I can be used to detect <strong>and</strong> ablate metastatic<br />

disease. Prophylactic nodal dissection is unwarranted because nodal involvement is<br />

. infrequent, but therapeutic neck dissection is recommended<br />

The cumulative percentage of patient mortality from follicular thyroid cancer is about<br />

15 percent at 10 years <strong>and</strong> 30 percent at 20 years. Factors that significantly worsen

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