THYROIDITIS
THYROIDITIS
 Thyroiditis usually is classified into acute,
subacute, and chronic forms.
Acute (Suppurative) Thyroiditis
 It is an acute inflammation of thyroid gland.
 Infectious agents can seed it (a) via the
hematogenous or lymphatic route,
 (b) via direct spread from persistent pyriform
sinus fistulae or thyroglossal duct cysts
 (c) as a result of penetrating trauma to the
thyroid gland,
 (d) due to immunosuppression.
 Acute suppurative thyroiditis is more common in
children and often is preceded by an upper
respiratory tract infection or otitis media.
 It is characterized by severe neck pain radiating
to the jaws or ear, fever, chills, odynophagia,
and dysphonia.
 Complications such as systemic sepsis, tracheal
or esophageal rupture, jugular vein thrombosis,
laryngeal chondritis, and perichondritis or
sympathetic trunk paralysis may also occur.
Diagnosis
 The diagnosis is established by leukocytosis on
blood tests and FNAB for Gram's stain, culture,
and cytology.
 CT scans may help to delineate the extent of
infection.
 A persistent pyriform sinus fistula should always
be suspected in children with recurrent acute
 thyroiditis. A barium swallow demonstrates the
anomalous tract with 80% sensitivity.
Treatment
 Treatment consists of parenteral
antibiotics
 Drainage of abscesses.
 Patients with pyriform sinus fistulae
require complete resection of the sinus
tract, including the area of the thyroid
where the tract terminates, to prevent
recurrence
Chronic
Thyroiditis
Lymphocytic (Hashimoto's) Thyroiditis
 Lymphocytic thyroiditis was first described
by Hashimoto in 1912 as struma
lymphomatosa—a transformation of
thyroid tissue to lymphoid tissue.
 It is the most common inflammatory
disorder of the thyroid and the leading
cause of hypothyroidism.
Etiology, Pathogenesis, and
Pathology
 Autoimmune disease
 Hypothyroidism results not only from the
destruction of thyrocytes by cytotoxic T
cells but by autoantibodies.
 Chronic thyroiditis also has been
associated with increased intake of iodine
and administration of medications such as
interferon- , lithium, and amiodarone.
Clinical Presentation
 Hashimoto's thyroiditis is also more common in women
(male:female ratio 1:10 to 20 ) between the ages of 30
and 50 years old.
 The most common presentation is that of a minimally or
moderately enlarged firm granular gland discovered on
routine physical examination or the awareness of a
painless anterior neck mass
 although 20% of patients present with hypothyroidism,
and
 5%present with hyperthyroidism (Hashitoxicosis).
 In classic goitrous Hashimoto's thyroiditis, physical
examination reveals a diffusely enlarged, firm gland,
which also is lobulated. An enlarged pyramidal lobe often
is palpable.
Diagnostic Studies
 When Hashimoto's thyroiditis is suspected
clinically, an elevated TSH and the presence of
thyroid autoantibodies usually confirm the
diagnosis.
 FNAB is indicated in patients who present with a
solitary suspicious nodule or a rapidly enlarging
goiter.
 Thyroid lymphoma is a rare but well-recognized,
ominous complication of chronic autoimmune
thyroiditis.
Treatment
 Thyroid hormone replacement therapy is indicated in
overtly hypothyroid patients, with a goal of maintaining
normal TSH levels. The
 management of patients with subclinical hypothyroidism
(normal T4 and elevated TSH) is controversial.
Treatment is advised
 especially for middle-aged patients with cardiovascular
risk factors such as hyperlipidemia or hypertension and
in pregnant
 patients.15 Treatment also is indicated in euthyroid
patients to shrink large goiters. Surgery may
occasionally be indicated for
 suspicion of malignancy or for goiters causing
compressive symptoms or cosmetic deformity
Riedel's Thyroiditis
 Riedel's thyroiditis is a rare variant of
thyroiditis also known as Riedel's struma
or invasive fibrous thyroiditis that is
characterized by
 the replacement of all or part of the thyroid
parenchyma by fibrous tissue, which also
invades into adjacent tissues.
Etiology
 The etiology of this disorder is controversial, and
it has been reported to occur in patients with
other autoimmune diseases. This association,
 coupled with the presence of lymphoid infiltration
and response to steroid therapy, suggests a
primary autoimmune etiology.
 Riedel's thyroiditis also is associated with other
focal sclerosing syndromes including
mediastinal, retroperitoneal, periorbital, and
 retro-orbital fibrosis and sclerosing cholangitis,
suggesting that it may, in fact, be a primary
fibrotic disorder.
Clinical picture
 The disease occurs predominantly in women
between the ages of 30 to 60 years old. It
typically presents as a painless, hard anterior
neck mass, which progresses over weeks to
years to produce symptoms of compression,
including dysphagia, dyspnea, choking, and
hoarseness.
 Patients may present with symptoms of
hypothyroidism and hypoparathyroidism as the
gland is replaced by fibrous tissue.
Diagnosis
 Physical examination reveals a hard,
"woody" thyroid gland with fixation to
surrounding tissues.
 The diagnosis needs to be confirmed by
open thyroid biopsy, because the firm and
fibrous nature of the gland renders FNAB
inadequate.
Treatment
 Surgery is the mainstay of the treatment. The
chief goal of operation is to decompress the
trachea by wedge excision of the thyroid isthmus
and to make a tissue diagnosis.
 More extensive resections are not advised due
to the infiltrative nature of the fibrotic process
that obscures usual landmarks and structures.

Treatment
 Hypothyroid patients are treated with
thyroid hormone replacement.
 Some patients who remain symptomatic
have been reported to experience
dramatic improvement after treatment with
corticosteroids and tamoxifen
6.1.THYROIDITIS.ppt
6.1.THYROIDITIS.ppt

6.1.THYROIDITIS.ppt

  • 1.
  • 2.
    THYROIDITIS  Thyroiditis usuallyis classified into acute, subacute, and chronic forms.
  • 3.
    Acute (Suppurative) Thyroiditis It is an acute inflammation of thyroid gland.  Infectious agents can seed it (a) via the hematogenous or lymphatic route,  (b) via direct spread from persistent pyriform sinus fistulae or thyroglossal duct cysts  (c) as a result of penetrating trauma to the thyroid gland,  (d) due to immunosuppression.
  • 4.
     Acute suppurativethyroiditis is more common in children and often is preceded by an upper respiratory tract infection or otitis media.  It is characterized by severe neck pain radiating to the jaws or ear, fever, chills, odynophagia, and dysphonia.  Complications such as systemic sepsis, tracheal or esophageal rupture, jugular vein thrombosis, laryngeal chondritis, and perichondritis or sympathetic trunk paralysis may also occur.
  • 5.
    Diagnosis  The diagnosisis established by leukocytosis on blood tests and FNAB for Gram's stain, culture, and cytology.  CT scans may help to delineate the extent of infection.  A persistent pyriform sinus fistula should always be suspected in children with recurrent acute  thyroiditis. A barium swallow demonstrates the anomalous tract with 80% sensitivity.
  • 6.
    Treatment  Treatment consistsof parenteral antibiotics  Drainage of abscesses.  Patients with pyriform sinus fistulae require complete resection of the sinus tract, including the area of the thyroid where the tract terminates, to prevent recurrence
  • 7.
  • 8.
    Lymphocytic (Hashimoto's) Thyroiditis Lymphocytic thyroiditis was first described by Hashimoto in 1912 as struma lymphomatosa—a transformation of thyroid tissue to lymphoid tissue.  It is the most common inflammatory disorder of the thyroid and the leading cause of hypothyroidism.
  • 9.
    Etiology, Pathogenesis, and Pathology Autoimmune disease  Hypothyroidism results not only from the destruction of thyrocytes by cytotoxic T cells but by autoantibodies.  Chronic thyroiditis also has been associated with increased intake of iodine and administration of medications such as interferon- , lithium, and amiodarone.
  • 10.
    Clinical Presentation  Hashimoto'sthyroiditis is also more common in women (male:female ratio 1:10 to 20 ) between the ages of 30 and 50 years old.  The most common presentation is that of a minimally or moderately enlarged firm granular gland discovered on routine physical examination or the awareness of a painless anterior neck mass  although 20% of patients present with hypothyroidism, and  5%present with hyperthyroidism (Hashitoxicosis).  In classic goitrous Hashimoto's thyroiditis, physical examination reveals a diffusely enlarged, firm gland, which also is lobulated. An enlarged pyramidal lobe often is palpable.
  • 11.
    Diagnostic Studies  WhenHashimoto's thyroiditis is suspected clinically, an elevated TSH and the presence of thyroid autoantibodies usually confirm the diagnosis.  FNAB is indicated in patients who present with a solitary suspicious nodule or a rapidly enlarging goiter.  Thyroid lymphoma is a rare but well-recognized, ominous complication of chronic autoimmune thyroiditis.
  • 12.
    Treatment  Thyroid hormonereplacement therapy is indicated in overtly hypothyroid patients, with a goal of maintaining normal TSH levels. The  management of patients with subclinical hypothyroidism (normal T4 and elevated TSH) is controversial. Treatment is advised  especially for middle-aged patients with cardiovascular risk factors such as hyperlipidemia or hypertension and in pregnant  patients.15 Treatment also is indicated in euthyroid patients to shrink large goiters. Surgery may occasionally be indicated for  suspicion of malignancy or for goiters causing compressive symptoms or cosmetic deformity
  • 13.
    Riedel's Thyroiditis  Riedel'sthyroiditis is a rare variant of thyroiditis also known as Riedel's struma or invasive fibrous thyroiditis that is characterized by  the replacement of all or part of the thyroid parenchyma by fibrous tissue, which also invades into adjacent tissues.
  • 14.
    Etiology  The etiologyof this disorder is controversial, and it has been reported to occur in patients with other autoimmune diseases. This association,  coupled with the presence of lymphoid infiltration and response to steroid therapy, suggests a primary autoimmune etiology.  Riedel's thyroiditis also is associated with other focal sclerosing syndromes including mediastinal, retroperitoneal, periorbital, and  retro-orbital fibrosis and sclerosing cholangitis, suggesting that it may, in fact, be a primary fibrotic disorder.
  • 15.
    Clinical picture  Thedisease occurs predominantly in women between the ages of 30 to 60 years old. It typically presents as a painless, hard anterior neck mass, which progresses over weeks to years to produce symptoms of compression, including dysphagia, dyspnea, choking, and hoarseness.  Patients may present with symptoms of hypothyroidism and hypoparathyroidism as the gland is replaced by fibrous tissue.
  • 16.
    Diagnosis  Physical examinationreveals a hard, "woody" thyroid gland with fixation to surrounding tissues.  The diagnosis needs to be confirmed by open thyroid biopsy, because the firm and fibrous nature of the gland renders FNAB inadequate.
  • 17.
    Treatment  Surgery isthe mainstay of the treatment. The chief goal of operation is to decompress the trachea by wedge excision of the thyroid isthmus and to make a tissue diagnosis.  More extensive resections are not advised due to the infiltrative nature of the fibrotic process that obscures usual landmarks and structures. 
  • 18.
    Treatment  Hypothyroid patientsare treated with thyroid hormone replacement.  Some patients who remain symptomatic have been reported to experience dramatic improvement after treatment with corticosteroids and tamoxifen