Thyroid Cancer

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Thyroid Cancer - Thyroid 101: Risky Business

  • Definition: Malignant tumor originating from thyroid follicular or parafollicular C cells.
  • Epidemiology:
    • ⭐ Most common endocrine malignancy.

    • India: Accounts for ~1-2% of all cancers; incidence rising.
  • Key Risk Factors:
    • Radiation exposure: Especially in childhood (< 15 yrs); dose-dependent (e.g., 5-10 Gy).
    • Family history: Syndromic (e.g., MEN2, FAP, Cowden syndrome) or non-syndromic familial thyroid cancer.
    • Iodine status: Deficiency (↑ follicular cancer risk); Excess (possible ↑ papillary cancer risk, debated).
    • Female gender.
    • Age extremes (childhood, >45 yrs).
    • Pre-existing benign thyroid conditions (e.g., goiter, adenomas).
  • Thyroid malignancies: follicular epithelial or parafollicular C-cell origin.
  • 📌 Papillary: Popular (~80%), Psammoma bodies, Positive Prognosis.

Histopathology of Thyroid Cancer Subtypes

FeaturePapillary (PTC)Follicular (FTC)Medullary (MTC)Anaplastic (ATC)
OriginFollicular cellsFollicular cellsParafollicular C-cellsDedifferentiated cells
Histo KeyOrphan Annie nuclei, Psammoma bodies, nuclear groovesCapsular/vascular invasion defines malignancyAmyloid stroma (Congo red+), spindle cellsMarked pleomorphism, high mitoses
GeneticsBRAF V600E, RET/PTCRAS, PAX8-PPARγRET (MEN2A/2B assoc.)TP53, BRAF, TERT
PrognosisExcellent, indolentGood, hematogenous spreadModerate, ↑CalcitoninDismal, highly aggressive

Thyroid Cancer - Nodule CSI: Case Cracked

  • Presentation: Solitary thyroid nodule (most common); hoarseness, dysphagia, stridor (compressive symptoms).
  • Diagnostic Workup:
    • USG: Initial. Suspicious: microcalcifications, hypoechogenicity, irregular margins, taller-than-wide, ↑vascularity. Ultrasound features of suspicious thyroid nodules
    • Serum TSH: If normal/high & USG suspicious → FNAC. If low → Radionuclide scan (cold nodule? → FNAC).
    • FNAC: Bethesda System (Categories I-Nondiagnostic to VI-Malignant). Bethesda System for Thyroid Cytology Overview
    • Serum Calcitonin: If Medullary Thyroid Cancer (MTC) suspected (family Hx, USG).
    • Serum Thyroglobulin (Tg): Post-op surveillance for differentiated cancers (PTC, FTC).

⭐ FNAC is the most important initial diagnostic test for a thyroid nodule.

Thyroid Cancer - Thyroid Takedown Tactics

  • Surgery: Primary treatment.
    • Total Thyroidectomy (TT): Standard for most.
    • Lobectomy: For small, low-risk unifocal DTC.
    • Neck Dissection: Nodal disease (therapeutic); prophylactic central for MTC.
  • Radioactive Iodine ($I^{131}$): Post-TT for DTC remnant/mets.
    • Ablation (30-100 mCi), adjuvant, metastatic disease.
  • TSH Suppression: Levothyroxine to ↓TSH, prevent recurrence.
    • High-risk: <0.1 mIU/L. Low-risk: 0.1-0.5 mIU/L.
  • Advanced/Refractory:
    • EBRT: Unresectable, residual disease, palliative.
    • Systemic: TKIs (Lenvatinib-DTC, Vandetanib-MTC), Chemo (ATC).

⭐ Differentiated thyroid cancers (papillary, follicular) are typically iodine-avid, making $I^{131}$ therapy effective.

Thyroid Cancer - Post-Op: The Long Haul

  • Prognostic Factors: Age (e.g., <55 yrs better), tumor size, extrathyroidal extension, histological type, molecular markers (e.g., BRAF).
  • Differentiated Thyroid Cancer (DTC) Follow-up:
    • Serum Thyroglobulin (Tg) & anti-Tg antibodies (key for recurrence).
    • Neck Ultrasound (USG).
  • Medullary Thyroid Cancer (MTC) Follow-up:
    • Serum Calcitonin & CEA levels.
    • Neck USG.

⭐ Rising Thyroglobulin (Tg) levels post-thyroidectomy in DTC strongly suggest recurrence or persistent disease.

High‑Yield Points - ⚡ Biggest Takeaways

  • Papillary Ca: Most common, Orphan Annie eyes, psammoma bodies, lymphatic spread, best prognosis.
  • Follicular Ca: Hematogenous spread, needs capsular/vascular invasion for diagnosis (not by FNAC alone).
  • Medullary Ca: From C-cells, linked to MEN2 (RET), secretes calcitonin (tumor marker).
  • Anaplastic Ca: Elderly, rapid growth, aggressive, worst prognosis.
  • FNAC: Best initial test for thyroid nodules.
  • Treatment: Total thyroidectomy then RAI ablation for differentiated (Papillary, Follicular) cancers.
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Treatment of esthesioneuroblastoma is _____ combined with preoperative chemotherapy or radiotherapy

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Treatment of esthesioneuroblastoma is _____ combined with preoperative chemotherapy or radiotherapy

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