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Thyroid Cancer
www.entnet.orgdecision for resection more challenging. An FNAB diagnosis of malignant
cells, however, is an obvious indication for surgery, either a total thyroid
lobectomy or a total thyroidectomy. Certainly, any evidence of thyroid can-
cer in the neck nodes is an indication for total thyroidectomy and appropri-
ate neck dissection.
Remember, that absent any risk factors, there is a high degree of probabil-
ity that the nodule is benign. If the pathologic interpretation on the FNAB
favors a benign histopathology and the patient does not have any other
risk factors for thyroid cancer, one can advocate observation. If the lab
report is indeterminant or inconclusive, a repeat FNAB with the aid of an
ultrasound is necessary to ensure sampling efficiency of the tissue. When
multiple nodules are found, the thyroid is classified as a
multinodular
thyroid or goiter,
and only the dominant or largest nodules are biopsied.
If a single nodule is determined to be inconclusive by FNAB, FNAB should
be repeated. Radionuclide
thyroid scans
have become less essential to the
diagnostic workup of nodules with the development and refinement of
ultrasound and fine-needle aspiration techniques.
Forms of Thyroid Cancer
There are two essential classifications of thyroid cancer: well differentiated
and other.
The more common forms of thyroid cancer are well differen-
tiated, and include papillary and follicular
(including the
Hürthle cell
variant). The “other” category includes less well-differentiated forms of
thyroid cancer, including
medullary,
and
anaplastic. Lymphoma may
also arise in the thyroid.
Papillary Carcinoma
Approximately 80 percent of thyroid cancers are papillary histologically.
These may have a
follicular component,
but any amount of papillary com-
ponent means the tumor will behave more like a papillary tumor. These
tumors
can be multifocal
in the gland and
often metastasize
to neck lymph
nodes. The presence of lymph node masses does not appear to affect sur-
vival rates. Histologically, they have
clear nuclei
(“Orphan Annie”
cells
),
and may have
psammoma
bodies. Factors predictive of a better prognosis
include small size (less than 1.5 centimeters (cm)) and absence of thyroid
gland capsule involvement. For unknown reasons, this disease follows a
much more indolent course when discovered in people under age 40. How-
ever, while papillary carcinoma patients under 40 years of age ultimately live
longer, they also experience a higher rate of recurrence.