Zusammenfassung der Ressource
Thyroid Tumors
- Benign
- Types
- Follicular Adenoma
- "Cold"
- Almost all
are cold
- May still produce
worrisome symptoms
- Compression of trachea
- Dysphagia
- "Hot"
- Functioning
- Clinical Findings
- Increased
radioactive iodine
uptake
- May have signs of
hyperthyroidism
- Subtypes
- Macro (colloid)
- Normo
- Micro
- Trabecular
- General
- Most common benign thyroid tumor
- Encapsulated tumor with
follicular differentiation
- Very low malignant potential
- Almost always solitary
- Treatment
- Partial or complete thyroidectomy
- Solitary Nodule
- Granular Cell Tumor
- Malignant
- Types
- Papillary Carcinoma
- General
- Most common thyroid malignancy
- F>M, 3:1
- a/w childhood radiation exposure
- Excellent prognosis
- Gross and
Microscopic Findings
- Multifocal
- Empty appearing nuclei
- Orphan Annie eyes
- Papillary projections within glandular space
- Psamomma bodies
- Collection of calcified cancer
cells; stain deep purple
- Lymphatic invasion
- Mets to cervical LNs and lung
- Diagnosis
and
Treatment
- Dx: FNA
- Partial or complete thyroidectomy
- Followed by
radiotherapy with
radioactive Iodine
- Suppression
therapy
- levothyroxine to increase
negative feedback on TSH
secretion
- Shrinks the tumor
- Follicular Carcinoma
- General
- F>M
- Good prognosis
- a/w radiation exposure (less so than
papillary) and iodine deficiency
- Gross and Microscopic Findings
- Usually a single cold, encapsulated nodule
- Haematogenous spread
Anmerkungen:
- Rather than lymphatic spread as seen in papillary carcinoma
- Mets to lung and bone first
- Well-differentiated, uniform follicles
- No psamomma bodies
- Widely invasive or minimally
invasive classification
Anmerkungen:
- Minimally invasive: capsule invasion only (may have some vascular invasion of a few small vessels)
Widely invasive: extends through capsule and into thyroid parenchyma and vasculature
- Hurthle cell carcinoma
often considered a variant
- Diagnosis and Treatment
- FNA is NOT diagnostic
- Microscopically the same as follicular adenoma
- Need evidence of invasion
- Definitive dx requires lobectomy
- Treated similarly to papillary carcinoma
- Medullary Carcinoma
- Findings
- Increased serum calcitonin
- Causes diarrhoea
- Tumor marker
- May have ectopic hormone production,
paraneoplastic syndromes
- Ex. ACTH causing Cushing syndrome
- Calcitonin amyloid material in stroma
- Mets
- Early regional LN mets common
- Distant mets to liver, lung, bone and brain
- Diagnosis and Treatment
- Dx: FNA, increased calcitonin
- Total thyroidectomy and genetic
screening of RET gene if familial
- General
- Neuroendocrine tumor of parafollicular C cells
- C-cell hyperplasia is a precursor lesion
- Causes
- Sporadic (80%)
- Poorer prognosis than familial type
- Unilateral
- Familial (20%)
- a/w MEN 2A and 2B
Anmerkungen:
- Recall:
MEN 2A- medullary carcinoma, hyperparathyroidism, pheochromocytoma
MEN 2B- medullary carcinoma, mucosal neuromas, pheochromocytoma
- Younger patients
- Bilateral and multicentric
- Anaplastic
- General
- Elderly women
- a/w multinodular goiter and positive follicular cancer history
- Rapidly aggressive
- VERY poor prognosis
- Early dissemination
- Invasion of local
structures (trachea,
oesophagus) common
- 50% have lung mets at presentation
- Gross and Microscopic
Findings
- Regions of spontaneous
haemorrhage and
necrosis
- Infiltration of adjacent structures
- Diagnosis and Treatment
- Dx: FNA or surgery if
inconclusive
- Palliative treatment
- Partial surgical
resection
- Tumor often
compresses the trachea
- Extensive resection of tumor
and surrounding structures
generally NOT indicated
- High post-op morbidity
- Ex. vocal cord paralysis
- No proven survival benefit
- Chemo or radiation
- Primary B Cell Lymphoma
- Most commonly a/w Hashimoto's thyroiditis