Thyroid cytopathology

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Thyroid cytopathology is a large part of cytopathology.

This article deals only with thyroid cytopathology. An introduction to cytopathology is in the cytopathology article. Head and neck cytopathology is dealt with in the Head and neck cytopathology article.

Normal

Follicular cells:

  • Uniform spacing of cells.
  • "Cracks" (spaces) between cell - "crazy paving".[1]

Colloid - acellular crap with:

  • Irregular/sharp borders.
  • Cracks - key feature.
  • Dark (uniform) staining with Romanowsky type stains.
    • Green edge + red/orange centre with Pap stain.
  • +/-Entraped red blood cells (RBCs).

Note:

  • It is interesting that uniform spacing in the context of thyroid is benign... in breast suggests DCIS.

Standard sign-out language

There is a standard way of describing thyroid cytopathology results.

Bethesda (2009)

This is formally known as the "The Bethesda System for Reporting Thyroid Cytopathology"; it is based on the NCI classification of 2008:[2]

Preferred Plain language Risk of malignancy Usual management
Benign Benign ~ 0-3% Follow-up, clinical
Follicular lesion of undetermined significance (FLUS)
or atypia of undetermined significance 		Uncertain, favour benign 5-15% Repeat FNA
Follicular neoplasm
or suspicious for follicular neoplasm; if oncocytic type it should be noted 		Uncertain, favour malignant 15-30% Hemithyroidectomy
Suspicious for malignancy Probably malignant 60-75% Repeat vs. hemithyroidectomy
Malignant Cancer ~ 97-99% Excise (total thyroidectomy)
Nondiagnostic or unsatisfactory Lesion missed or inadequate 1-4% Repeat FNA

NCI (2008)

A National Cancer Institute (NCI) consensus conference in 2008:[3]

Preferred (NIC) Alternate (NIC) Plain language Risk of malignancy Usual management
Benign - Benign ~ 1% Follow/nothing
Follicular lesion of undetermined significance (FLUS) 1. Atypia of undetermined significance
2. Rule-out neoplasm
3. Atypical follicular lesion
4. Cellular follicular lesion 		Uncertain, favour benign 5-10% Repeat FNA in 3 months
Follicular neoplasm Suspicious for follicular neoplasm Uncertain, favour malignant 20-30% Hemithyroidectomy
Hurthle cell neoplasm Suspicious for Hurthle cell neoplasm Uncertain, favour malignant 20-30% Hemithyroidectomy
Suspicious for malignancy - Probably malignant 50-75% Repeat vs. hemithyroidectomy
Malignant - Cancer ~ 99% Excise
Nondiagnostic - Lesion missed or inadequate Unknown Repeat FNA in 3 months

Graves disease

Main article: Graves disease

General

  • Clinical diagnosis - based on serology.

Cytology

Features:

  • +/-Flame cells on Romanowsky stain, e.g. Diff-Quik.[4]
    • Red granular discolourization of the cytoplasm - thought to be endoplasmic reticulum.

Images:

Lymphocytic thyroiditis

General

Cytology

Features:

  1. Lymphocytes not typical of circulating blood:
    • Centrocytes.
      • Small lymphocytes with a cleft.
    • Centroblasts.
      • Large lymphocytes with nucleolus and eccentric nucleus.
    • Plasma cells.
      • Cells with a "clockface nucleus".
  2. Small mature lymphocytes in fragments of follicular cells - raise the suspicion of lymphocytic thyroiditis.[5]
    • Small mature lymphocytes are not a reliable indicator of inflammation, as cells may layer during tissue preparation.[6]

Notes:

  • Usually #1 and #2 are seen.

Hashimoto thyroiditis

Main article: Hashimoto thyroiditis

General

  • This is a clinical diagnosis.
    • It should be reported by the pathologist as "lymphocytic thyroiditis".

Associations:[1][7]

  • AMA +ve.
  • Antithyroid antibody +ve.
    • Antimicrosomal (antithyroid peroxidase).
    • Antithyroglobulin.
  • Increased risk of B-cell lymphoma.

Cytology

Features:[1]

  • Polymorphous lymphoplasmacytic infiltrate with germinal centres.
  • Tingible body macrophages.
    • Found in germinal centres; have condensed chromatin fragments.[8]
  • Lymphoid tangles.
    • Found in almost 100% of cases.[7]
  • Lymphoglandular bodies.
    • Cytoplasmic fragment of a lymphoid cell.[9]

Follicular lesion of undetermined significance

Abbreviated FLUS.

General

  • This is waffle diagnosis, i.e. something the pathologist diagnoses when they cannot decide whether it is benign or suspicious for malignant (follicular neoplasm or suspicious for malignancy).[10]
    • Like all waffle diagnoses...
      • Use should be minimized; < 7% is suggested, though it varies considerably between pathologists and institutions.[10]

Cytology

Features:

  • Mild nuclear atypia - that by definition is insufficient for follicular neoplasm or suspicious for malignancy.
    • Mild irregularities in the nuclear contour.
    • Mild size variation or nuclear enlargement.
    • Mild accentuation of nuclear staining.

Papillary carcinoma

Main article: Papillary thyroid carcinoma
  • Papillary thyroid carcinoma is basically the only entity (in cytopathology) that has near universally accepted criteria.
    • This is why radiation oncologists say... "Basing stuff on pathology is like basing something on shifting sand."

Cytology

Criteria for papillary thyroid carcinoma:[11][12]

  1. Nuclear inclusion (really pseudoinclusions):[13]
    1. Edge of inclusion must be sharp (nuclear membrane-like).
    2. Size: at least 1/4 of the nucleus.
    3. Round, regular.
    4. Within epithelial cell.
    • Additional criteria:[14] Inclusion center should match cytoplasm.
  2. Nucleoli (micro or macro).
  3. Nuclear grooves.
    • No universal criteria; some believe grooves should go from edge-to-edge, i.e. across the nucleus.
  4. Nuclear enlargement.
  5. Changes in chromatin - patterns:
    • Granular.
    • Washed-out.

Additional features:

  • Papillary architecture (not commonly seen).
    • Clump of epithelial cells with attached fibrous tissue "tail" - that has a smooth edge.
  • Cellular/nuclear membrane overlapping; cells do not respect one another (very common).
  • +/-Psammoma bodies (uncommon - but helpful if seen).

Notes:

  • Nuclear enlargement may be seen in Hashimoto's disease.[15]
  • Nuclear grooves may be seen in Hashimoto's disease.[16]
  • Papillary architecture may be seen in Graves disease.[17]

Variants of PTC

  • Tall cell variant.
    • May mimic Hurthle cell neoplasm.
  • Warthin-like variant.
    • Superficially resembles Warthin tumour (presence of lymphocytes).
  • Follicular variant of PTC; memory device ECT: Elongation, Clearing, Thick membranes.
    • Nuclear elongation.
    • Chromatin clearing.
    • Thick nuclear membranes.
      • Classic features of PTC (esp. pseudo-inclusions) are usually scarce in this variant.

Follicular neoplasm

  • Sort of a garbage category for the thyroid.

Cytology

Features:[3]

  1. Hypercellular lesion.
  2. 3-dimensional clusters of cells.
  3. Nuclear overlap/crowding.
  4. +/-Microfollicles, numerous.
    • Microfollicles are defined as: <15 cells forming at least two thirds of a circle.
  5. +/-Atypia marked.

Diagnosis (follicular neoplasm) per MB:

  • Either: 1-3 or 3-5.

Notes:

  • A few microfollicles are normal.
  • Atypia alone - "suspicious for malignancy" or "malignant".

Management:

  • Hemithyroidectomy.

Oncocytic neoplasm (Hurthle cell neoplasm)

General:

  • Oncocytic perferred by WHO over Hurthle cell.

Features:[3]

  1. Single cells or sheets of oncocytic cells.
    • 3-D clusters.
    • +/-Transgressing vessels - cluster of oncocytes surrounding vessels.
  2. Oncocytic cells:
    • Well-defined cellular borders.
    • Finely granular abundant cytoplasm.
    • Nucleoli, may be prominent.

Notes:

  • Benign (oncocytic) thyroid tissue may have:
    • Significant nuclear pleomorphism.
    • Multinucleation.

Diagnosis by MB:

  • If single cells -- need abundant.

Image:

Medullary thryoid carcinoma

Main article: Medullary thyroid carcinoma
  • May be familial - associated with MEN II syndrome.

Cytology

Features:[3]

  1. Single or loosely cohesive cells.
    • Spindle cell morphology common.
  2. Abundant eosinophilc granular cytoplasm - key feature
  3. Salt and pepper chromatin - key feature; no nucleoli.
  4. Nucleus eccentric and round/oval - plasmacytoid appearance.
  5. Amyloid - acellular, amorphous material may be present; cotton candy-like.
    • May be confused with fibrin...
      • Fibrin = fluffy edge vs. amyloid = sharp border. (???)
      • Fibrin - associated with PMNs/has PMNs within it.
    • Amyloid cannot be definitively differentiated on morphologic grounds from colloid.
    • Described by Halliday et al. as:[18]
      • Romanowsky type staining: "amorphous, irregular, waxy basophilic to metachromatic clump".
      • Pap staining: "cyanophilic-organophilic clumps of material + occasional prominent fissures".

Notes:

DDx:

  • Anaplastic carcinoma.

Images:

IHC

  • Calcitonin +ve - it arises from C cells (which produce calcitonin)
  • CEA +ve (often better staining than calcitonin).[20]
  • Congo-red +ve (if amyloid present) - mnemonic: CRAP -- congo red amyloid protein.

Anaplastic carcinoma

  • Prognosis: very crappy.

Cytology

Features:

  • Nuclear atypia - marked.
  • Spindle cell morphology common.
  • Nucleolus.
  • Usually scant cellularity.[21]
  • Necrosis very common.

DDx:

  • Medullary carcinoma.

See also

References

  1. ↑ 1.0 1.1 1.2 Lefkowitch, Jay H. (2006). Anatomic Pathology Board Review (1st ed.). Saunders. pp. 672. ISBN 978-1416025887.
  2. ↑ Cibas ES, Ali SZ (November 2009). "The Bethesda System for Reporting Thyroid Cytopathology". Thyroid 19 (11): 1159–65. doi:10.1089/thy.2009.0274. PMID 19888858.
  3. ↑ 3.0 3.1 3.2 3.3 Baloch ZW, LiVolsi VA, Asa SL, et al. (June 2008). "Diagnostic terminology and morphologic criteria for cytologic diagnosis of thyroid lesions: a synopsis of the National Cancer Institute Thyroid Fine-Needle Aspiration State of the Science Conference". Diagn. Cytopathol. 36 (6): 425-37. doi:10.1002/dc.20830. PMID 18478609.
  4. ↑ 4.0 4.1 URL: http://moon.ouhsc.edu/kfung/jty1/CytoLearn/CytoQuiz/CQ-021-040/CQ-037-M.htm. Accessed on: 10 April 2012.
  5. ↑ GD. 2 February 2010.
  6. ↑ SB. ~29 January 2010.
  7. ↑ 7.0 7.1 Poropatich C, Marcus D, Oertel YC (1994). "Hashimoto's thyroiditis: fine-needle aspirations of 50 asymptomatic cases". Diagn. Cytopathol. 11 (2): 141-5. PMID 7813361. http://www3.interscience.wiley.com/journal/112701408/abstract?CRETRY=1&SRETRY=0.
  8. ↑ MacLennan I.C.M (1994). "Germinal Centers". Annual Review Immunology 12: 117-139. PMID 8011279.
  9. ↑ URL: http://www.definition-of.com/lymphoglandular+body. Accessed on: 27 January 2012.
  10. ↑ 10.0 10.1 Layfield LJ, Morton MJ, Cramer HM, Hirschowitz S (October 2009). "Implications of the proposed thyroid fine-needle aspiration category of "follicular lesion of undetermined significance": A five-year multi-institutional analysis". Diagn. Cytopathol. 37 (10): 710–4. doi:10.1002/dc.21093. PMID 19373907.
  11. ↑ SM. 12 January 2010.
  12. ↑ Kini SR. Guides to clinical aspiration biopsy: thryoid. 2nd Ed. 1996. P.134.
  13. ↑ Boerner SL, Asa SL. Biopsy Interpretation of the Thyroid. Lippincott Williams & Wilkins. ISBN 978-0-7817-7204-4. PP.112-3.
  14. ↑ SB. 8 January 2010.
  15. ↑ WG. 8 January 2010.
  16. ↑ WG. 8 January 2010.
  17. ↑ Biopsy Interpretation of the Thyroid. PP.97-98.
  18. ↑ Halliday BE, Silverman JF, Finley JL (April 1998). "Fine-needle aspiration cytology of amyloid associated with nonneoplastic and malignant lesions". Diagn. Cytopathol. 18 (4): 270–5. PMID 9557261. http://www3.interscience.wiley.com/cgi-bin/fulltext/39158/PDFSTART.
  19. ↑ URL: http://www.papsociety.org/guidelines/Morphologic%20criteria.doc. Accessed on: 28 April 2010.
  20. ↑ SB. 7 January 2010.
  21. ↑ GS. March 2, 2010.
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