Difference between revisions of "Pulmonary cytopathology"
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| Cytoplasm | | Cytoplasm | ||
| Scant | | Scant | ||
| Abundant, bubbly | | Abundant, bubbly, +/-'''vacuole with mucin''' | ||
| Abundant, "dense" | | Abundant, "dense" | ||
| Abundant r/o small cell | | Abundant r/o small cell, <br>mucin vacuole r/i adenocarcinoma | ||
|- | |- | ||
| Streaming | | Streaming |
Revision as of 21:05, 20 May 2010
Pulmonary cytopathology is a subset of cytopathology.
This article deals only with pulmonary cytopathology (FNAs, sputum samples). An introduction to cytopathology is in the cytopathology article.
Normal
- Cells with cilia = good.
- Cells with "terminal bar" (apical red band-like region associated with cilia) = good.
Specimens
- Bronchial brushings.
- Bronchial washing (contain airway cells).
- Bronchoalveolar lavage (BAL).
- Endobronchial ultrasongraphic transbronchial needle aspiration (EBUS-TNA).
Adequacy
- Want to see pulmonary macrophages (large cells with bubbly green/brown cytoplasm, eccentric reniform nucleus).
- Ciliated cells may be from the nasopharynx - not proof of lung parenchymal tissue.
There is no generally accepted standard for pulmonary specimens. An in-house standard is:[1]
- Sputum: >= 10 pulmonary macrophages.
Pulmonary hamartoma
Histology:
- No cytologic features of malignancy.
- Fat.
Non-specific inflammation
- A very common finding in BALs.
Types:
- Eosinophilia
- If you notice eosinophils... you probably have eosinophilia.
- One in several HPFs (40x obj. with 22 mm eye piece) is enough.
- If you notice eosinophils... you probably have eosinophilia.
- Acute - neutrophils.
- ~10/HPF (40xo 22mm ep).
- Chronic - lymphocytes + occ. plasma cells.
- ~5 small lymphocytes/HPF (40xo 22 mm ep).
- Mixed acute & chronic inflammation.
Infection
If you see lotsa lymphocytes think tumour.[2]
Pneumocystic carinii pneumonia (PCP)
Features:
- Casts of frothy material/large proteinaceous debris - approximately the size of an alveolus.
Aspergillosis
Features:
- Hyphae... branching at 45 degrees.
Image:
Zygomycosis
- AKA mucormycosis.
Features:
- Hyphae... with variable width.
Image:
Crytococcus
Features:
- Prominent (i.e. thick polysaccharide) capsule.
- Seen well on Pap stain... harder to see on rapid Romanowsky stain.
- Spherical - 5-15 micrometres.
Image:
DDx:
- Bastomycosis.
- Doesn't have thick capsule
- Has broad based budding.
- Coccidioidomycosis - larger (20-60 micrometers).
Cancer
Approaches to lung cancer
Lung cancer in a table
Small cell carcinoma | Adenocarcinoma | Squamous cell carcinoma | Value | |
---|---|---|---|---|
Cellular cohesion | Single cells/stripped nuclei common | Cohesive | Cohesive | Cohesive (only) suggests NSCLC |
Nuclear moulding | Present | Absent | Absent | R/i & r/o: small cell carcinoma and carcinoid |
Small nucleoli (difficult to see on Field stain) | Multiple pseudo-nucleoli may be seen in occ. cells | Many be present | Often present | Weak discriminative valuable |
Large nucleoli | Never | Present | Rarely | R/i adenocarcinoma; should prompt consideration of melanoma briefly |
Location of nucleus | Eccentric | Eccentric | Central | Useful for SCC vs. adenocarcinoma |
Cytoplasm | Scant | Abundant, bubbly, +/-vacuole with mucin | Abundant, "dense" | Abundant r/o small cell, mucin vacuole r/i adenocarcinoma |
Streaming | Absent | Absent | Present - "stretched yeast dough" | R/i squmaous (weak) |
Keratin (difficult to see on Field stain) | Absent | Absent | Present | Present r/i squamous (strong) |
Criteria list
Neuroendocrine tumours - look for:
- Nuclear moulding (not seen in NSCLC).
- Singular bare nuclei/single cells - often very abundant in small cell lung carcinoma (SCLC).
- Size ~2X neutrophil (PMN) - SCLC is large relative to most haematologic cancers (which are approx. the size of a PMN)... small in relation to other carcinoma.[3]
- Stippled chromatin.
- Negatives: Abundant cytoplasm - virtually excludes SCLC.
- Carcinoid vs. atypical carcinoid vs. SCLC (list from good to bad) - degree of nuclear atypia, presence of necrosis and smoking history.
- One should never sign-out small cell carcinoma without looking at the history.[4]
Adenocarcinoma:
- Nucleolus.
- Good ones are visible with 10X objective (excludes SCLC).
- Look for subtle large ones - at higher power.
- Neuroendocrine tumours occasionally may appear to have nucleoli - one should see good nucleoli in 3-4 cells in one field.
- Abundant cytoplasm - virtually excludes small cell carcinoma.
- Vacuoles with mucin (pink discolouration) - virtually diagnostic, though only seen occasionally.
- Eccentric nucleus.
- Negatives: NO moulding.
- Important if no nucleolus obvious.
Squamous cell carcinoma:
- Small nucleolus - not visible at 10X.
- Coarse chromatin.
- "Streaming" - think stringy yeast dough.
- Keratin (orange) - on Pap stain.
Adenocarcinoma
- Most common type of lung cancer.
Cytology
Features:
- Nucleolus.
- Good ones are visible with 10X objective (virtually excludes SCLC).
- Look for subtle large ones - at higher power.
- Abundant cytoplasm - virtually excludes small cell carcinoma.
- Vacuoles with mucin (pink discolouration) - virtually diagnostic.
- Eccentric nucleus.
- Negatives: NO moulding.
- Important if no nucleolus visible.
Notes:
- May be subtle, i.e. have minimal cytologic changes.
DDx:
- Benign mesothelium (also sheets of cells).
- Atypical adenomatous hyperplasia (AAH) - thought to be the precursor to adenocarcinoma.[5]
- AAH has a size criterion, ergo not really possible to diagnose on cytopathology specimen.
Neuroendocrine tumours
- This is a group of tumours that has benign (e.g. carcinoid tumour of the lung) to malignant (e.g. small cell lung carcinoma) behaviour.[6]
The grouping can be divided into four types:[7]
- Small cell carcinoma.
- Large cell neuroendocrine carcinoma.
- Typical carcinoid.
- Atypical carcinoid.
Cytologic features useful for differentiation:
- Small cell carcinoma: necrosis, scant cytoplasm, mitoses.
- Typical carcinoid: often more cytoplasm, no necrosis, low mitotic rate (MIB-1: scant staining).
- Atypical carcinoid: higher mitotic rate/MIB-1 than typical carcinoid,[8] no necrosis.
Notes:[7]
- Large cell and small cell tumours behave in a similar fashion; large cell can be considered a morphological variant of small cell.
- 9/10 of carcinoids are typical and usually have a good prognosis, i.e. do not metastasize.
- Central location (vis-a-vis peripheral location) tends favours typical carcinoid over atypical carcinoid.
Small cell lung carcinoma
- Is the most easy lung cancer to miss, as one is usually looking for large cells.
Histology:
- Morphologic features of malignancy:
- Irregular nuclear membrane.
- Chromatin clumping.
- Marked nuclear size variation.
- Bare nuclei common - very useful if present.
- Nuclear moulding - key feature.
- Stippled chromatin - key feature.
- Small cells ~ 2x RBC.
- Scant cytoplasm - so scant it often near impossible to see.
Notes:
- The Azzopardi phenomenon (smudging of nuclei) is not present on cytology specimens - it is processing artifact.
- Small cell carcinoma should not be diagnosed without a clinical history; if there is no smoking history... think about the possibility of carcinoid and atypical carcinoid.
- Small cell leukemias may mimic small cell carcinoma; difference: leukemias typically have smaller cells (~size of RBC vs. ~2x of RBC), and lymphoglandular bodies.
Image:
Squamous cell carcinoma
Microscopic
- Mix of spindle cells/epithelioid cells, present in clusters, +/-small number of single cells.
- Keratinization:
- Orange/red staining on Pap stain.
- Poorly differentiated SCC = not orange/red.
- "Intense" (blue) staining of cells on rapid Romanowsky + pyknotic (small shriveled) nucleus.[9]
- Orange/red staining on Pap stain.
- "Dense" appearing cytoplasm.
- +/-Laminae (layers)/lines in the cytoplasm.
- Nuclear features of malignancy (required for diagnosis):
- Irregular nuclear membrane, e.g. notches, sharp discontinuities.
- Nuclear hyperchromasia - "jet-black" nuclei on Pap stain key feature.
- Increased NC ratio.
- Variation of nuclear size from cell-to-cell.
Image(s):
Notes:
- One should see abnormal squamous cells to call it SCC.
- The default diagnosis is usually adenocarcinoma.
- Poorly differentiated SCC may look like adenocarcinoma.
Malignant melanoma
Classic features:
- Loosely cohesive cells and single cells.
- Mixure of epithelioid cells and spindle cells.
- Malignant cells have:
- Prominent red nucleolus.
- Pigmented cytoplasm - key feature (often not pigmented).
- Pigment may only be present in macrophages
- Occasional large binucleated cells (bug-eyed monster cell).
- Nuclei are often at opposite poles of the cell, i.e. the nuclei are as far apart as possible ("divorce cells").[10]
- Intranuclear inclusions.
- Pigmented macrophages (useful feature - but less specific for melanoma than pigment in malignant looking cells).
Notes:
- Large nucleolus - may Vaguely resemble adenocarcinoma.
- Prominent red nucleolus common in: serous carcinoma.
- The classic appearance of melanoma without pigment is closest to adenocarcinoma (which may have red nucleoli, large cells, abundant cytoplasm, occasional binucleation).
- Differentiating morphologic features: adenocarcinoma - 3-D clusters of cells, no spindle-shaped cells.
- Bug-eyed monster cells - may vaguely resemble a Reed-Sternberg cell (RSC) - diagnostic of Hodgkin's lymphoma (HL).
- RSCs do not have the granular cytoplasm typical of melanoma.
- Nuclei usually adjacent, i.e. not at opposite poles of the cell.
- Background of melanoma different than HL.
Images:
See also
References
- ↑ UHN PCY50001.08 P.11.
- ↑ Attributed to SM. 6 January 2010.
- ↑ WG. 20 January 2010.
- ↑ WG. 20 January 2010.
- ↑ Mori, M.; Rao, SK.; Popper, HH.; Cagle, PT.; Fraire, AE. (Feb 2001). "Atypical adenomatous hyperplasia of the lung: a probable forerunner in the development of adenocarcinoma of the lung.". Mod Pathol 14 (2): 72-84. doi:10.1038/modpathol.3880259. PMID 11235908. http://www.nature.com/modpathol/journal/v14/n2/full/3880259a.html.
- ↑ URL: http://emedicine.medscape.com/article/426400-overview. Accessed on: 20 January 2010.
- ↑ 7.0 7.1 http://www.cancer.org/docroot/CRI/content/CRI_2_4_1X_What_is_lung_carcinoid_tumor_56.asp
- ↑ WG. February 2010.
- ↑ GS. 24 February 2010.
- ↑ GS. 24 February 2010.