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THE NECK MASS General Sx Topic
Reviewed and present by Mr. Patinya Yutchawit, Miss Kaewalin Thongsawangjang, Miss Withunda
Akaapimand,
Miss Rattanaporn Sirirattanakul, Miss Tritraporn Sawantranon, Mr. Yotdanai Namuangchan, Mr.
THYROID Introduction and
anatomy
Follicles -> Lobule
Principal cells (ie, follicular) formation of the colloid
(iodothyroglobulin),
Parafollicular cells :calcitonin
Superior thyroid artery
Inferior thyroid artery
Thyroidima artery
Superior thyroid artery
Inferior thyroid artery
Thyroidima artery
Superior thyroid vein
Middle thyroid vein
Inferior thyroid veins
Nerve
Parasympathetic fibers vagus nerves
Sympathetic fibers : superior, middle, and inferior
ganglia of the sympathetic trunk.
APPROACH TO NECK
MASS
Start
access
• Origin
• Cause
Hx
• ความชุกชุมของโรค
• อายุ
• เพศ
• ระยะเวลา
• ความเจ็บปวด
• อาการทั่วไป : ไข้ อ่อนเพลีย เสียงแหบ กลืนลาบาก ไอเลือดปน น้ามูก
ปนเลือด หูอื้อข้างเดียว เลือดกาเดาไหลบ่อย แน่นจมูก แผลที่ศีร ะ คอ
ช่องปาก ลิ้น
PE
• Local examination
• Regional examination
• General examination
Local examination
• Location
• Size > 1.5 cm , <1.5cm. 2ข้าง
• Shape
• Surface
• Consistency
• Tenderness
• Fluctuation
• Tranlumination
• Attachment
• Skin
• Punctum
• Pulsation
• Miscellaneaeous: move follow tongue prtusion,swallowing
Location
Mid line Ant. Triangle Post. Triangle
Congenital
-thyroglossal duct cyst
-dermoid cyst
-laryngocele
Inflammation
-adenditis
Tumor
-thyroid
-lymphoma
Other
-sternocleidomastoid
hematoma/fibroma
Congenital
-brachial cleft cyst
-thymic cyst
-sialadenopathy
(parotid,submandibular)
Inflammation
-adenitis(viral,bact.,
glanulomatous)
-sialadenitis
Tumor
-metastasic
-upper jugular
-submandibular
-middle jugular
-lymphoma
-vascular(carotid tumor,
hemangioma)
Other
- False aneurysm
Congenital
-lymphangioma
Inflammation
-adenitis(viral,bact.,
glanulomatous)
Tumor
-lymphoma
-metastatic
-supraclavicular
Other
Neuroma
investigation
• Blood
– CBC, ESR, LFT, Ca, heteropliie Ab, HIV Ab, EBV Ab
• Imaging
– X-ray, U/S, CT, MRI (submucosal),radionuclide scan
– sialography
• Cytology
– FNA
• Tissue
– biopsy
THYROGLOSSAL DUCT
CYST
THYROGLOSSAL DUCT CYST
Neck mass that
develops from
cells and tissues
remaining after
the formation of
the thyroid gland
during
embryonic
development
Pathogenesis
• The primitive thyroid descended from its
origin at the base of the tongue to its
permanent location, low in the neck. Failure of
subsequent closure and obliteration of this
tract predisposes to thyroglossal cyst
formation.
Types of thyroglossal duct cysts
–Infrahyoid type : 65 %
–Suprahyoid type : 20 %
–Juxtahyoid cysts : 15 %
–Intralingual location
–Suprasternal variety
–Intralaryngeal
Clinical presentation
• A small,soft,round mass
in the midline of neck
• Mass rise with swallowing or
protrusion of the tongue
•It is most commonly
diagnosed in preschool-
aged children or during
mid-adolescence
CLINICAL PRESENTATION
Infected cysts may manifest as
tender masses with
Dysphagia
Draining sinus
Fever
Enlarging neck mass
Diagnosis
• Clinical : upward when tongue is extended and
swallowing
• Contain thyroid tissue
– TFT
– Thyroid scan
–Ultrasound
a midline infrahyoid unilocular mass
with a homogeneously hypoechoic internal
echotexture, typical of a TDC.
Pathology
• Cyst cavity
and thyroid tissue
On rare occasion,
turn to carcinoma
Treatment
• Antibiotic if infected
• Surgery : Sistrunk’s Operation
- Removal of the cyst, the tract, and
the central portion of the hyoid bone as
well as a portion of the tongue base up
to the foramen cecum.
Solitary
thyroid nodule
Euthyroid Hyperthyroid
FNA biopsy cytology
I-131/Sx
FSH,FT3
Hot
nodule
Cold
nodule
TMG
Thyroid scan
TSH FT3
FNA
Reaspirate
Benign
Solid/Mix
NegativeSuspiciousPositive
Malignant
Hormone
suppressive,F/U
Sx Sx
LobectomySx +/- I-131
Cyst
GRAVE’S DISEASE
Graves’ Disease
• Graves’s disease , Primary toxic goiter , Basedow’s
disease , Exopthalmicgoiter
• autoimmune disease : antibody against the
thyroid-stimulating hormone (TSH) receptor
(Thyroid stimulating immunoglobulin ,TSI)
stimulates the gland to synthesize and secrete
excess thyroid hormone
• Characterized by hyperthyroidism, diffuse goiter,
opthalmopathy and, sometimes, dermopathy.
• Most common cause of hyperthyroidism
Age: 20-50 years
Sex: female : male 7-8:1
60-90% of all causes of
thyrotoxicosis
100-200 cases /100,000
population /year
EPIDEMIOLOGY
• 50 % Genetic inheritance
• Other factors, such as smoking, sex
steroids, life stresses, and dietary iodine
intake, bacterial or viral infection are
possible causes of Graves’ disease
ETIOLOGY
• 1.Increase metabolic rate of all cells
• 2.Increase sensitivity of beta-adrenergic
receptors
• 3.Stimulate all cells to grow
Thyroid hormone effects
Metabolic:
ravenous appetite, weight loss, excessive
sweating, heat intolerance
CVS:
Palpitations, shortness of breath, tiredness,
irregular heart beat
CNS:
irritability, insomnia, depression
CLINICAL
• GI:
Change in appetite and weight, Increase
frequency of bowel movement, diarrhea
• RP:
reduction in the quantity of menses,
amenorrhea, decreased fertility,
increased incidence of miscarriages
• MS:
wasting and weakness of small muscle of
hand, shoulder, face
• GA: looks thin and wasting of face and hands,
sweating
• CVS: tachycardia at rest, persist during sleep.
AF, collapsing pulses, heart failure
• CNS: fine tremor
• Skin: warm and moist, pretibial myxedema
• MS: muscle wasting, proximal muscle weakness,
hyperactive tendon reflex, digital clubbing
Physical examination
• Signs in the neck
Diffused, symmetrically enlarged thyroid gland
Systolic bruit audible over its lateral lobe,palpable
thrill
• Signs in the eyes
Lid retraction and lid lag
Exopthalmos
Ophthalmoplegia: proptosis, limitation of upward and
latral gaze
Chemosis: conjunctival swelling and congestion
Physical examination
 Thyroid function test
High T3, T4 ; Low TSH
 Thyroid stimulating antibodies (TSAb)
 123I uptake and scan : Increase
Diagnostic tests
•Medication
•Radioactive 131I
•Thyroidectomy
Management
• Beta blocker : Propranolol 20-40 mg qid
offer relief of the adrenergic symptoms
of hyperthyroidism such as tremor,
palpitations, heat intolerance, and
nervousness
Medication
• Reserve for
- Small, non toxic goiters less than 40 g
- Mildly elevated thyroid hormone levels
- Rapid decrease in gland size with antithyroid
medication
• PTU: 100-300 mg tid
• MMI: 10-30 md tid, then once daily
• Side effects: skin rash, fever, vasculitis,rarely
agranulocytosis, aplastic anemia
• High relapse rate when discontinued drug 1-2 year (40-
80%)
Antithyroid drugs
Medication
• Recommended in
- Older patients with small or moderate-size goiter
- Relapse after medical or surgical therapy
- Antithyroid drugs or surgery are contraindicated
Radioactive Iodine therapy
• Woman who are pregnant or breastfeeding
Relative contraindications
• Children and adolescent
• Patient with thyroid nodule
• Patient with ophthalmopathy
Absolute contraindications
Radioactive Iodine therapy
Recommend in
- RAI is contraindication
- Have confirmed cancer or suspicious thyroid nodules
- Young
- Pregnant or desire to conceive soon after treatment
- Severe reaction to antithyroid medication or poor
compliance
- Large goiters causing compressive symptoms or for
cosmetic reason
- Reluctant to undergo RAI therapy
Surgical treatment
• Euthyroid by continue antithyroid drug until
the day of surgery
• Lugol’s iodine solution or saturated K iodine 3
drops bid for 7-10 day preoperatively →
reduce vascularity of gland and decrease risk
of precipitating thyroid storm
Prep. For surgery
Hemithyroidectomy - Entire isthmus is removed along
with 1 lobe. Done in benign diseases of only 1 lobe.
Subtotal thyroidectomy- Done in toxic thyroid, primary
or secondary, and also for toxic multinodular goiter
(MNG).
Partial thyroidectomy - Removal of gland in front of
trachea after mobilization. Done in nontoxic MNG. Its
role is controversial.
Near total thyroidectomy- Both lobes are removed
except for a small amount of thyroid tissue (on one or
both sides) in the vicinity of the recurrent laryngeal
nerve entry point and the superior parathyroid gland.
Done in papillary thyroid carcinoma.
Total thyroidectomy- Entire gland is removed. Done in
case of follicular carcinoma of thyroid, medullary
carcinoma of thyroid.
Hartley Dunhill operatio - Removal of 1 entire lateral
• Total or near total thyroidectomy
- Coexistent thyroid cancer
- Refuse RAI
- Severe ophthalmopathy
- Life threatening reaction to antithyroid
medication e.g. vasculitis, agranulocytosis, liver
failure
* High rate of hypothyroidism
• Subtotal thyroidectomy (4-7 g remain)
- All remaining patients
Higher recurrent rate of hyperthyroidism
Bleeding
Hypocalcemia
Recurrent laryngeal nerve injury
Superior laryngeal nerve injury
Thyroid crisis
COMPLICATION
THYROID CANCER
• Benign follicular adenoma
• Malignant : primary
– Follicular epithelium-differentiated : papillary
,follicular
– Follicular epithelium-undiffentiated : anaplstic
– Parafollicular cells : medullary
– Lymphoid cells : lymphoma
• Malignant : Secondary
- Metastasis
Thyroid cancer
THYROID CANCER
Follicular epithilial – differentiated
 Papillary carcinoma (75 – 80%)
 Follicular carcinoma (15 – 20 %)
Follicular epithilial – undifferentiated
 Anaplastic carcinoma (<5%)
Parafollicular cell
 Medullary carcinnoma (5%)
Lymphoid cell
 lymphoma
PAPILLARY CARCINOMA
Most common thyroid cancer***
Age 30-50 years old
Risk factor = Previous exposure to Ionizing radiation
Most common presentation = Asymptomatic thyroid
mass/nodule
Excellent prognosis = 10 years survival rate >95%
SPREADING
Lymphatic spreading (35-43%)
Blood vessels invasion (40%)
Distant metastasis (3-7%)
SIGNS AND SYMPTOMS
Asymptomatic Thyroid mass
If advanced CA
 Hoarsness
 Dysphagia
 Cough
 Dyspnea
INVESTIGATION
Fine Needle Aspiration
Ultrasonography
 distinguish solid from cystic lesions and identify calcifications
Thyroid scan
 Cold nodule
HISTOPATHOLOGY
mixed papillary and follicular growth patterns
Orphan Annie eye nuclei (= characteristic pale empty
nuclei)
Papillary finger-like projection
Psammoma body
FOLLICULAR
CARCINOMA
2nd common thyroid cancer
High incidence in iodine-depleted
countries
Common in patient > 50 years
Closely resemble to follicular
adenoma  capsular or vascular
invasion is defined malignat
status
Hematologic spreading  distant
metastasis difficult to control
May be involve cervical lymph
node
10-year survival rate > 90%
Here comes your footer ▫ Page *
•follicular carcinomas demonstrate capsular invasion (B, arrow-heads) that may be
minimal, as in this case, or widespread with extension into local structures of the
neck. The presence of vascular invasion is another feature of follicular carcinomas.
•Hurthle cell tumor-Variant of follicular
Neoplasm in which oxyphil cells predominate
histology
• recurrent laryngeal nerve palsy 2-7%
• permanent hypoparathyroidism 1-3%
• hematoma 1-2%
• wound infection < 1%
• hypertrophy of the scar
• anaplastic carcinomas are aggressive tumors, with a mortality rate
approaching 100%. Survival calculated in months
• mean age of 65 years.
• About half of the patients have a history of multinodular goiter, Spread by
lymphatic and by the bloodstream
Here comes your footer ▫ Page *
Anaplastic carcinoma
ANAPLASTIC CARCINOMA
Here comes your footer ▫ Page *
Here comes your footer ▫ Page *
highly anaplastic cells, which may take one of several histologic patterns: (1) large,
pleomorphic giant cells, including occasional osteoclast-like multinucleate giant
cells; (2) spindle cells with a sarcomatous appearance; (3) mixed spindle and giant
cells; and (4) small cells resembling those seen in small cell carcinomas arising at
other sites.
• Advanced or metastatic disease
– no effective therapy for advanced or metastatic anaplastic
thyroid cancer
– median survival from diagnosis ranges from three to seven
months
– Death is usually attributable to upper airway obstruction
– Radiation therapy does not prolong survival, most have
local recurrences
– Chemotherapy response duration is generally short, and
long-term survival (as well as local control in the neck)
probably unaffected
MEDULLARY CARCINOMA
Tumors of Parafollicular cells (C cells) derived from
neural crest
Neuroendocrine neoplasms
Secrete Calcitonin (useful in diagnosis and follow up)
INCIDENCE
80% of cases are sporadical tumors
Age 50-60 years old
Lymphatic metastasis 50-60%
May occur in combination known as MEN 2A or 2B
SIGNS AND SYMPTOMS
a lump at the base of the neck, which may interfere with
or become more prominent during swallowing.
If locally advanced disease : hoarseness, dysphagia, and
respiratory difficulty.
Various paraneoplastic syndromes, including Cushing or
carcinoid syndrome (uncommon)
+/- Diarrhea
Distant metastases : weight loss, lethargy, and bone pain
INVESTIGATION
Serum Calcitonin level
 The higher the greater of likelihood to be MTC
 Basal level >100 pg/mL
PATHOLOGY
Medullary carcinoma of
thyroid. These tumors
typically show a solid
pattern of growth and do
not have connective tissue
capsules
Medullary carcinoma of
the thyroid. These tumors
typically contain amyloid
stroma
STAGING
TREATMENT
Total Thyroidectomy
Prophylactic/Therapeutic resection of central and
bilateral cervical lymph nodes
POSTOPERATIVE
MANAGEMENT
Thyroxine therapy maintain euthyroidism
adjuvant therapy with radioiodine
SURGERY FOR RESIDUAL DISEASE
Serum calcitonin and CEA should be measured 6 months
after surgery detect the presence of recurrence
WRAP-UP! Approach to neck
mass
THE HALF-BAKED
CONCEPT
IS OKAY, AS LONG AS
IT’S IN THE OVEN.
Let’s continue baking!
CASE : A PAINLESS LUMP
IN THE NECK
History
A 40-year-old woman has been referred to the
surgical outpatients with a painless lump in the
neck. She had noticed the lump 2 weeks
previously when looking in the mirror.
She had not noticed any other lumps and does
not complain of any other symptoms. She has
not gained or lost any weight recently and her
bowel habit has remained normal.
CASE : A PAINLESS LUMP
IN THE NECK
Examination
Examination reveals a solitary 2x2 cm swelling
to the left of the midline just above the
manubrium. The swelling is firm, smooth and
fixed. The swelling moves on swallowing, but
does not move on protrusion of the tongue.
There are no associated palpable lymph glands.
General examination reveals no further
abnormalities.
INVESTIGATION
Hemoglobin 12.0 g/dL
Mean cell volume 77 fL
White cell count 10.4x109/L
Platelets 250x109/L
Sodium 137 mmol/L Potassium 3.7 mmol/L
Urea 5 mmol/L (2.5–6.7
mmmol/L)
Creatinine 71 μmol/L (44–80
μmol/L)
Thyroid-stimulating hormone (TSH) 0.62mu/L
(0.5–5.7 mu/L)
Free tri-iodothyronine (T3) 3.4 pmol/L (2.5–
5.3 pmol/L)
QUESTIONS
1. What is the differential diagnosis for a lump in
the anterior triangle of the neck?
2. Where is this lump likely to be originating from?
3. What steps would you take in the assessment of
this lump?
4. Which factors may suggest malignancy?
5. What are the commonest types of malignancy?
TAKE YOUR FRIEND’S
ANSWER SHEET, TAKE A
LOOK AND GIVE THEM
GRADE.
Talk about it.
WHAT IS THE DIFFERENTIAL
DIAGNOSIS FOR A LUMP IN THE
ANTERIOR TRIANGLE OF THE
NECK?
Multiple: lymph nodes
Solitary: does it move
with
swallowing?
• yes:
- thyroid origin
- thyroglossal cyst
(moves with protrusion
of the tongue)
• no:
- salivary gland
- dermoid cyst
- carotid body
tumur
- lymph node
- branchial cyst
- cold abscess (TB)
WHERE IS THIS LUMP LIKELY
TO BE ORIGINATING FROM?
… to the left of the midline just above the manubrium
… The swelling moves on swallowing, but does not move
on protrusion of the tongue.
“Thyroid origin”
The majority of patients are clinically euthyroid and have
normal thyroid function. The presence of abnormal
thyroid function suggests a benign diagnosis.
WHAT STEPS WOULD YOU
TAKE IN THE ASSESSMENT OF
THIS LUMP?
Less than 20 per cent of thyroid nodules are malignant,
with the majority being cystic or benign. Many solitary
thyroid nodules are dominant nodules in a multinodular
goitre,which carry a 5 per cent risk of malignancy.
Ultrasound is used to distinguish between solid and
cystic nodules as well as differentiating a solitary nodule
from a dominant nodule in a multinodular goitre.
Fine-needle aspiration has a high sensitivity and
specificity for distinguishing benign from malignant
lumps in the thyroid. The main limitation of fine-needle
aspiration is in the differentiation of benign follicular
adenoma from malignant follicular cancer. If a follicular
neoplasm is diagnosed on fine-needle aspiration, the
lesion will need to be fully excised to exclude
malignancy.
WHAT STEPS WOULD YOU
TAKE IN THE ASSESSMENT OF
THIS LUMP?
Radio-isotope scanning provides a functional
assessment of the thyroid nodule, which can be
classified as cold or hot.
Most solitary thyroid nodules are cold, with a risk of
cancer at around 20 per cent.
WHICH FACTORS MAY
SUGGEST MALIGNANCY?
• age younger than 20 years or older than 70 years
• male sex
• recent origin and rapid growth or increase in size
• firm, hard, or immobile nodule
• presence of cervical lymphadenopathy
• associated symptoms of dysphagia or dysphonia
• history of neck irradiation
• prior history of thyroid carcinoma or a positive family
history.
WHAT ARE THE COMMONEST
TYPES OF MALIGNANCY?
Type frequency age Behavior Prog
Papillary 70% 20-40s Slow growing,
lymphatic spread
to nodes
Good
10 yr 80%
Follicular 20% 35-50s Bloodstream spread,
metastasis to lung
and bone
Good
10 yr 60%
Anaplastic <5% 60-70s Aggressive, local
spread
Poor
10 yr 10%
Medullary 5% Familial From parafollicular
C cell, MEN
TAKE’EM HOME! A brief review.
POINTS
>20% of adult neck masses are malignant
70% of pediatric neck masses are infectious in nature
Know your anatomy then develop a differential diagnosis
Close observation
Generally, one course of a broad spectrum antibiotic is
acceptable then ….. It is never wrong to refer to a specialist
for evaluation and probable biopsy
Imaging is important but tissue is everything
If you don’t get an answer with a FNA, repeat it up to three
times. Consider ultrasound guided or CT guided FNA.
Never violate a neck if you’ve no idea about it.
POINTS
Avoid excisional biopsies
Use CT but consider MRI for
salivary gland problems
Role of nonionizing
ultrasound
Like a stethoscope
REFERENCE
- An introduction to the symptoms and sing of surgical
disease:
Norman L.Browse
- Bailey and Love's Short Practice of Surgery - 25th
Edition
- 100 cases in surgery
- พื้นฐานศัลยศาสตร์และอาการของโรคศัลยกรรมสาหรับแพทย์เวชปฏิบัติทั่วไป
คณะแพทยศาสตร์ ม.ศรีนครินทรวิโรฒ
- ตารา หู คอ จมูก คณะแพทยศาสตร์ ม.ขอนแก่น
- Uptodate : neck mass
HEY GUY! FIN.
DO YOU HAVE SOME
QUESTIONS??
Thank you for
your attention.

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Neck mass

  • 1. THE NECK MASS General Sx Topic Reviewed and present by Mr. Patinya Yutchawit, Miss Kaewalin Thongsawangjang, Miss Withunda Akaapimand, Miss Rattanaporn Sirirattanakul, Miss Tritraporn Sawantranon, Mr. Yotdanai Namuangchan, Mr.
  • 3.
  • 4.
  • 5. Follicles -> Lobule Principal cells (ie, follicular) formation of the colloid (iodothyroglobulin), Parafollicular cells :calcitonin
  • 6. Superior thyroid artery Inferior thyroid artery Thyroidima artery
  • 7. Superior thyroid artery Inferior thyroid artery Thyroidima artery
  • 8. Superior thyroid vein Middle thyroid vein Inferior thyroid veins
  • 9. Nerve Parasympathetic fibers vagus nerves Sympathetic fibers : superior, middle, and inferior ganglia of the sympathetic trunk.
  • 10.
  • 12.
  • 13.
  • 14.
  • 16. Hx • ความชุกชุมของโรค • อายุ • เพศ • ระยะเวลา • ความเจ็บปวด • อาการทั่วไป : ไข้ อ่อนเพลีย เสียงแหบ กลืนลาบาก ไอเลือดปน น้ามูก ปนเลือด หูอื้อข้างเดียว เลือดกาเดาไหลบ่อย แน่นจมูก แผลที่ศีร ะ คอ ช่องปาก ลิ้น
  • 17. PE • Local examination • Regional examination • General examination
  • 18. Local examination • Location • Size > 1.5 cm , <1.5cm. 2ข้าง • Shape • Surface • Consistency • Tenderness • Fluctuation • Tranlumination • Attachment • Skin • Punctum • Pulsation • Miscellaneaeous: move follow tongue prtusion,swallowing
  • 19.
  • 20.
  • 21.
  • 22.
  • 23.
  • 24. Location Mid line Ant. Triangle Post. Triangle Congenital -thyroglossal duct cyst -dermoid cyst -laryngocele Inflammation -adenditis Tumor -thyroid -lymphoma Other -sternocleidomastoid hematoma/fibroma Congenital -brachial cleft cyst -thymic cyst -sialadenopathy (parotid,submandibular) Inflammation -adenitis(viral,bact., glanulomatous) -sialadenitis Tumor -metastasic -upper jugular -submandibular -middle jugular -lymphoma -vascular(carotid tumor, hemangioma) Other - False aneurysm Congenital -lymphangioma Inflammation -adenitis(viral,bact., glanulomatous) Tumor -lymphoma -metastatic -supraclavicular Other Neuroma
  • 25.
  • 26.
  • 27.
  • 28.
  • 29. investigation • Blood – CBC, ESR, LFT, Ca, heteropliie Ab, HIV Ab, EBV Ab • Imaging – X-ray, U/S, CT, MRI (submucosal),radionuclide scan – sialography • Cytology – FNA • Tissue – biopsy
  • 30.
  • 31.
  • 32.
  • 34. THYROGLOSSAL DUCT CYST Neck mass that develops from cells and tissues remaining after the formation of the thyroid gland during embryonic development
  • 35. Pathogenesis • The primitive thyroid descended from its origin at the base of the tongue to its permanent location, low in the neck. Failure of subsequent closure and obliteration of this tract predisposes to thyroglossal cyst formation.
  • 36.
  • 37.
  • 38.
  • 39. Types of thyroglossal duct cysts –Infrahyoid type : 65 % –Suprahyoid type : 20 % –Juxtahyoid cysts : 15 % –Intralingual location –Suprasternal variety –Intralaryngeal
  • 40. Clinical presentation • A small,soft,round mass in the midline of neck • Mass rise with swallowing or protrusion of the tongue •It is most commonly diagnosed in preschool- aged children or during mid-adolescence
  • 41.
  • 42. CLINICAL PRESENTATION Infected cysts may manifest as tender masses with Dysphagia Draining sinus Fever Enlarging neck mass
  • 43.
  • 44. Diagnosis • Clinical : upward when tongue is extended and swallowing • Contain thyroid tissue – TFT – Thyroid scan –Ultrasound
  • 45. a midline infrahyoid unilocular mass with a homogeneously hypoechoic internal echotexture, typical of a TDC.
  • 46.
  • 47. Pathology • Cyst cavity and thyroid tissue On rare occasion, turn to carcinoma
  • 48. Treatment • Antibiotic if infected • Surgery : Sistrunk’s Operation - Removal of the cyst, the tract, and the central portion of the hyoid bone as well as a portion of the tongue base up to the foramen cecum.
  • 49.
  • 50.
  • 51. Solitary thyroid nodule Euthyroid Hyperthyroid FNA biopsy cytology I-131/Sx FSH,FT3 Hot nodule Cold nodule TMG Thyroid scan TSH FT3 FNA Reaspirate Benign Solid/Mix NegativeSuspiciousPositive Malignant Hormone suppressive,F/U Sx Sx LobectomySx +/- I-131 Cyst
  • 53.
  • 54. Graves’ Disease • Graves’s disease , Primary toxic goiter , Basedow’s disease , Exopthalmicgoiter • autoimmune disease : antibody against the thyroid-stimulating hormone (TSH) receptor (Thyroid stimulating immunoglobulin ,TSI) stimulates the gland to synthesize and secrete excess thyroid hormone • Characterized by hyperthyroidism, diffuse goiter, opthalmopathy and, sometimes, dermopathy. • Most common cause of hyperthyroidism
  • 55.
  • 56. Age: 20-50 years Sex: female : male 7-8:1 60-90% of all causes of thyrotoxicosis 100-200 cases /100,000 population /year EPIDEMIOLOGY
  • 57. • 50 % Genetic inheritance • Other factors, such as smoking, sex steroids, life stresses, and dietary iodine intake, bacterial or viral infection are possible causes of Graves’ disease ETIOLOGY
  • 58. • 1.Increase metabolic rate of all cells • 2.Increase sensitivity of beta-adrenergic receptors • 3.Stimulate all cells to grow Thyroid hormone effects
  • 59. Metabolic: ravenous appetite, weight loss, excessive sweating, heat intolerance CVS: Palpitations, shortness of breath, tiredness, irregular heart beat CNS: irritability, insomnia, depression CLINICAL
  • 60. • GI: Change in appetite and weight, Increase frequency of bowel movement, diarrhea • RP: reduction in the quantity of menses, amenorrhea, decreased fertility, increased incidence of miscarriages • MS: wasting and weakness of small muscle of hand, shoulder, face
  • 61. • GA: looks thin and wasting of face and hands, sweating • CVS: tachycardia at rest, persist during sleep. AF, collapsing pulses, heart failure • CNS: fine tremor • Skin: warm and moist, pretibial myxedema • MS: muscle wasting, proximal muscle weakness, hyperactive tendon reflex, digital clubbing Physical examination
  • 62. • Signs in the neck Diffused, symmetrically enlarged thyroid gland Systolic bruit audible over its lateral lobe,palpable thrill • Signs in the eyes Lid retraction and lid lag Exopthalmos Ophthalmoplegia: proptosis, limitation of upward and latral gaze Chemosis: conjunctival swelling and congestion Physical examination
  • 63.
  • 64.
  • 65.  Thyroid function test High T3, T4 ; Low TSH  Thyroid stimulating antibodies (TSAb)  123I uptake and scan : Increase Diagnostic tests
  • 67. • Beta blocker : Propranolol 20-40 mg qid offer relief of the adrenergic symptoms of hyperthyroidism such as tremor, palpitations, heat intolerance, and nervousness Medication
  • 68. • Reserve for - Small, non toxic goiters less than 40 g - Mildly elevated thyroid hormone levels - Rapid decrease in gland size with antithyroid medication • PTU: 100-300 mg tid • MMI: 10-30 md tid, then once daily • Side effects: skin rash, fever, vasculitis,rarely agranulocytosis, aplastic anemia • High relapse rate when discontinued drug 1-2 year (40- 80%) Antithyroid drugs Medication
  • 69. • Recommended in - Older patients with small or moderate-size goiter - Relapse after medical or surgical therapy - Antithyroid drugs or surgery are contraindicated Radioactive Iodine therapy
  • 70. • Woman who are pregnant or breastfeeding Relative contraindications • Children and adolescent • Patient with thyroid nodule • Patient with ophthalmopathy Absolute contraindications Radioactive Iodine therapy
  • 71. Recommend in - RAI is contraindication - Have confirmed cancer or suspicious thyroid nodules - Young - Pregnant or desire to conceive soon after treatment - Severe reaction to antithyroid medication or poor compliance - Large goiters causing compressive symptoms or for cosmetic reason - Reluctant to undergo RAI therapy Surgical treatment
  • 72. • Euthyroid by continue antithyroid drug until the day of surgery • Lugol’s iodine solution or saturated K iodine 3 drops bid for 7-10 day preoperatively → reduce vascularity of gland and decrease risk of precipitating thyroid storm Prep. For surgery
  • 73. Hemithyroidectomy - Entire isthmus is removed along with 1 lobe. Done in benign diseases of only 1 lobe. Subtotal thyroidectomy- Done in toxic thyroid, primary or secondary, and also for toxic multinodular goiter (MNG). Partial thyroidectomy - Removal of gland in front of trachea after mobilization. Done in nontoxic MNG. Its role is controversial. Near total thyroidectomy- Both lobes are removed except for a small amount of thyroid tissue (on one or both sides) in the vicinity of the recurrent laryngeal nerve entry point and the superior parathyroid gland. Done in papillary thyroid carcinoma. Total thyroidectomy- Entire gland is removed. Done in case of follicular carcinoma of thyroid, medullary carcinoma of thyroid. Hartley Dunhill operatio - Removal of 1 entire lateral
  • 74. • Total or near total thyroidectomy - Coexistent thyroid cancer - Refuse RAI - Severe ophthalmopathy - Life threatening reaction to antithyroid medication e.g. vasculitis, agranulocytosis, liver failure * High rate of hypothyroidism • Subtotal thyroidectomy (4-7 g remain) - All remaining patients Higher recurrent rate of hyperthyroidism
  • 75. Bleeding Hypocalcemia Recurrent laryngeal nerve injury Superior laryngeal nerve injury Thyroid crisis COMPLICATION
  • 76.
  • 77.
  • 79. • Benign follicular adenoma • Malignant : primary – Follicular epithelium-differentiated : papillary ,follicular – Follicular epithelium-undiffentiated : anaplstic – Parafollicular cells : medullary – Lymphoid cells : lymphoma • Malignant : Secondary - Metastasis
  • 81. THYROID CANCER Follicular epithilial – differentiated  Papillary carcinoma (75 – 80%)  Follicular carcinoma (15 – 20 %) Follicular epithilial – undifferentiated  Anaplastic carcinoma (<5%) Parafollicular cell  Medullary carcinnoma (5%) Lymphoid cell  lymphoma
  • 82. PAPILLARY CARCINOMA Most common thyroid cancer*** Age 30-50 years old Risk factor = Previous exposure to Ionizing radiation Most common presentation = Asymptomatic thyroid mass/nodule Excellent prognosis = 10 years survival rate >95%
  • 83. SPREADING Lymphatic spreading (35-43%) Blood vessels invasion (40%) Distant metastasis (3-7%)
  • 84. SIGNS AND SYMPTOMS Asymptomatic Thyroid mass If advanced CA  Hoarsness  Dysphagia  Cough  Dyspnea
  • 85. INVESTIGATION Fine Needle Aspiration Ultrasonography  distinguish solid from cystic lesions and identify calcifications Thyroid scan  Cold nodule
  • 86. HISTOPATHOLOGY mixed papillary and follicular growth patterns Orphan Annie eye nuclei (= characteristic pale empty nuclei) Papillary finger-like projection Psammoma body
  • 87.
  • 88. FOLLICULAR CARCINOMA 2nd common thyroid cancer High incidence in iodine-depleted countries Common in patient > 50 years Closely resemble to follicular adenoma  capsular or vascular invasion is defined malignat status Hematologic spreading  distant metastasis difficult to control May be involve cervical lymph node 10-year survival rate > 90%
  • 89. Here comes your footer ▫ Page * •follicular carcinomas demonstrate capsular invasion (B, arrow-heads) that may be minimal, as in this case, or widespread with extension into local structures of the neck. The presence of vascular invasion is another feature of follicular carcinomas. •Hurthle cell tumor-Variant of follicular Neoplasm in which oxyphil cells predominate histology
  • 90.
  • 91.
  • 92.
  • 93. • recurrent laryngeal nerve palsy 2-7% • permanent hypoparathyroidism 1-3% • hematoma 1-2% • wound infection < 1% • hypertrophy of the scar
  • 94.
  • 95. • anaplastic carcinomas are aggressive tumors, with a mortality rate approaching 100%. Survival calculated in months • mean age of 65 years. • About half of the patients have a history of multinodular goiter, Spread by lymphatic and by the bloodstream Here comes your footer ▫ Page * Anaplastic carcinoma
  • 96. ANAPLASTIC CARCINOMA Here comes your footer ▫ Page *
  • 97. Here comes your footer ▫ Page * highly anaplastic cells, which may take one of several histologic patterns: (1) large, pleomorphic giant cells, including occasional osteoclast-like multinucleate giant cells; (2) spindle cells with a sarcomatous appearance; (3) mixed spindle and giant cells; and (4) small cells resembling those seen in small cell carcinomas arising at other sites.
  • 98.
  • 99.
  • 100. • Advanced or metastatic disease – no effective therapy for advanced or metastatic anaplastic thyroid cancer – median survival from diagnosis ranges from three to seven months – Death is usually attributable to upper airway obstruction – Radiation therapy does not prolong survival, most have local recurrences – Chemotherapy response duration is generally short, and long-term survival (as well as local control in the neck) probably unaffected
  • 101. MEDULLARY CARCINOMA Tumors of Parafollicular cells (C cells) derived from neural crest Neuroendocrine neoplasms Secrete Calcitonin (useful in diagnosis and follow up)
  • 102. INCIDENCE 80% of cases are sporadical tumors Age 50-60 years old Lymphatic metastasis 50-60% May occur in combination known as MEN 2A or 2B
  • 103. SIGNS AND SYMPTOMS a lump at the base of the neck, which may interfere with or become more prominent during swallowing. If locally advanced disease : hoarseness, dysphagia, and respiratory difficulty. Various paraneoplastic syndromes, including Cushing or carcinoid syndrome (uncommon) +/- Diarrhea Distant metastases : weight loss, lethargy, and bone pain
  • 104. INVESTIGATION Serum Calcitonin level  The higher the greater of likelihood to be MTC  Basal level >100 pg/mL
  • 105. PATHOLOGY Medullary carcinoma of thyroid. These tumors typically show a solid pattern of growth and do not have connective tissue capsules Medullary carcinoma of the thyroid. These tumors typically contain amyloid stroma
  • 107. TREATMENT Total Thyroidectomy Prophylactic/Therapeutic resection of central and bilateral cervical lymph nodes
  • 108. POSTOPERATIVE MANAGEMENT Thyroxine therapy maintain euthyroidism adjuvant therapy with radioiodine SURGERY FOR RESIDUAL DISEASE Serum calcitonin and CEA should be measured 6 months after surgery detect the presence of recurrence
  • 109. WRAP-UP! Approach to neck mass
  • 110. THE HALF-BAKED CONCEPT IS OKAY, AS LONG AS IT’S IN THE OVEN. Let’s continue baking!
  • 111. CASE : A PAINLESS LUMP IN THE NECK History A 40-year-old woman has been referred to the surgical outpatients with a painless lump in the neck. She had noticed the lump 2 weeks previously when looking in the mirror. She had not noticed any other lumps and does not complain of any other symptoms. She has not gained or lost any weight recently and her bowel habit has remained normal.
  • 112. CASE : A PAINLESS LUMP IN THE NECK Examination Examination reveals a solitary 2x2 cm swelling to the left of the midline just above the manubrium. The swelling is firm, smooth and fixed. The swelling moves on swallowing, but does not move on protrusion of the tongue. There are no associated palpable lymph glands. General examination reveals no further abnormalities.
  • 113. INVESTIGATION Hemoglobin 12.0 g/dL Mean cell volume 77 fL White cell count 10.4x109/L Platelets 250x109/L Sodium 137 mmol/L Potassium 3.7 mmol/L Urea 5 mmol/L (2.5–6.7 mmmol/L) Creatinine 71 μmol/L (44–80 μmol/L) Thyroid-stimulating hormone (TSH) 0.62mu/L (0.5–5.7 mu/L) Free tri-iodothyronine (T3) 3.4 pmol/L (2.5– 5.3 pmol/L)
  • 114. QUESTIONS 1. What is the differential diagnosis for a lump in the anterior triangle of the neck? 2. Where is this lump likely to be originating from? 3. What steps would you take in the assessment of this lump? 4. Which factors may suggest malignancy? 5. What are the commonest types of malignancy?
  • 115. TAKE YOUR FRIEND’S ANSWER SHEET, TAKE A LOOK AND GIVE THEM GRADE. Talk about it.
  • 116. WHAT IS THE DIFFERENTIAL DIAGNOSIS FOR A LUMP IN THE ANTERIOR TRIANGLE OF THE NECK? Multiple: lymph nodes Solitary: does it move with swallowing? • yes: - thyroid origin - thyroglossal cyst (moves with protrusion of the tongue) • no: - salivary gland - dermoid cyst - carotid body tumur - lymph node - branchial cyst - cold abscess (TB)
  • 117. WHERE IS THIS LUMP LIKELY TO BE ORIGINATING FROM? … to the left of the midline just above the manubrium … The swelling moves on swallowing, but does not move on protrusion of the tongue. “Thyroid origin” The majority of patients are clinically euthyroid and have normal thyroid function. The presence of abnormal thyroid function suggests a benign diagnosis.
  • 118. WHAT STEPS WOULD YOU TAKE IN THE ASSESSMENT OF THIS LUMP? Less than 20 per cent of thyroid nodules are malignant, with the majority being cystic or benign. Many solitary thyroid nodules are dominant nodules in a multinodular goitre,which carry a 5 per cent risk of malignancy. Ultrasound is used to distinguish between solid and cystic nodules as well as differentiating a solitary nodule from a dominant nodule in a multinodular goitre. Fine-needle aspiration has a high sensitivity and specificity for distinguishing benign from malignant lumps in the thyroid. The main limitation of fine-needle aspiration is in the differentiation of benign follicular adenoma from malignant follicular cancer. If a follicular neoplasm is diagnosed on fine-needle aspiration, the lesion will need to be fully excised to exclude malignancy.
  • 119. WHAT STEPS WOULD YOU TAKE IN THE ASSESSMENT OF THIS LUMP? Radio-isotope scanning provides a functional assessment of the thyroid nodule, which can be classified as cold or hot. Most solitary thyroid nodules are cold, with a risk of cancer at around 20 per cent.
  • 120. WHICH FACTORS MAY SUGGEST MALIGNANCY? • age younger than 20 years or older than 70 years • male sex • recent origin and rapid growth or increase in size • firm, hard, or immobile nodule • presence of cervical lymphadenopathy • associated symptoms of dysphagia or dysphonia • history of neck irradiation • prior history of thyroid carcinoma or a positive family history.
  • 121. WHAT ARE THE COMMONEST TYPES OF MALIGNANCY? Type frequency age Behavior Prog Papillary 70% 20-40s Slow growing, lymphatic spread to nodes Good 10 yr 80% Follicular 20% 35-50s Bloodstream spread, metastasis to lung and bone Good 10 yr 60% Anaplastic <5% 60-70s Aggressive, local spread Poor 10 yr 10% Medullary 5% Familial From parafollicular C cell, MEN
  • 122. TAKE’EM HOME! A brief review.
  • 123. POINTS >20% of adult neck masses are malignant 70% of pediatric neck masses are infectious in nature Know your anatomy then develop a differential diagnosis Close observation Generally, one course of a broad spectrum antibiotic is acceptable then ….. It is never wrong to refer to a specialist for evaluation and probable biopsy Imaging is important but tissue is everything If you don’t get an answer with a FNA, repeat it up to three times. Consider ultrasound guided or CT guided FNA. Never violate a neck if you’ve no idea about it.
  • 124. POINTS Avoid excisional biopsies Use CT but consider MRI for salivary gland problems Role of nonionizing ultrasound Like a stethoscope
  • 125.
  • 126. REFERENCE - An introduction to the symptoms and sing of surgical disease: Norman L.Browse - Bailey and Love's Short Practice of Surgery - 25th Edition - 100 cases in surgery - พื้นฐานศัลยศาสตร์และอาการของโรคศัลยกรรมสาหรับแพทย์เวชปฏิบัติทั่วไป คณะแพทยศาสตร์ ม.ศรีนครินทรวิโรฒ - ตารา หู คอ จมูก คณะแพทยศาสตร์ ม.ขอนแก่น - Uptodate : neck mass
  • 127. HEY GUY! FIN. DO YOU HAVE SOME QUESTIONS?? Thank you for your attention.