Definition
A malignant epithelial tumour composed of small cells with scant cytoplasm, finely granular nuclear chromatin and inconspicuous nucleoli. There is nuclear moulding and a high mitotic count.
Combined small cell carcinoma consists of small cell carcinoma in conjunction with a non-small cell component, commonly squamous cell carcinoma, adenocarcinoma or large cell carcinoma, less often sarcomatoid carcinoma.
Hoarseness and vocal cord palsy are more common, stridor and haemoptysis less common, than for squamous cell carcinoma. Clinical symptoms are often attributable to distant metastases. Paraneoplastic effects are common.
Hilar and mediastinal masses are often seen due to metastases at presentation, while the primary tumour is not radiographically apparent.
There is commonly no clear architecture, but there may be nesting trabeculae, peripheral palisading or rosette formation. Cells are small with scant cytoplasm and round to spindle nuclei, with fine chromatin and lacking conspicuous nucleoli. Nuclear moulding is common. Crush artefact is common. Larger specimens tend to show larger nuclei with some giant cells and more prominent nucleoli12. The mitotic rate is usually over 60 /10 HPF. The Azzopardi effect is seen, consisting of encrustation of blood vessels with nuclear basophilic material. Paranuclear blue inclusions may be useful in the cytological diagnosis of small cell carcinoma,although they are also seen in other small round cell tumours of childhood16.
Combined small cell carcinoma includes a non-small cell component. Since scattered large cells are common in small cell carcinoma, if this component is large cell carcinoma, it has been proposed that must comprise at least 10% of the tumour12.
See immunohistochemistry of malignant epithelial tumours of lung.
positive |
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positive |
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positive |
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positivity for at least one neuroendocrine marker |
>90% of cases |
||
90% |
|||
49/5920 |
|||
cytokeratins |
variable, often punctate |
||
positive6 |
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positive6 |
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Transcription factor E2F1 |
24/265 |
||
2/3310 |
|||
22/3018 |
|||
Loss of heterozygocity is common on 3p17 in small cell carcinoma of lung. LOH at the MEN1 gene locus occurs in the spectrum of neuroendocrine tumours of lung13. The patterns of p53 gene mutations were different between atypical carcinoid and high grade neuroendocrine tumours of lung13. Loss of expression due to hypermethylation appears to be more common in small cell and large cell lung carcinoma than in other types14. Caspase-8 expression is lost in neuroendocrine tumours of the lung but not in non-small cell carcinomas15.
CD56, cytokeratins, TTF-1 and CD45-are useful in the diagnosis of small cell lung carcinoma in biopsies with extensive crush artefact and can help confirm the diagnosis in cases where features are equivocal19.
|
small cell carcinoma |
lymphoid lesions |
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uncrushed cells |
crushed areas |
|
|||
CD56 |
20/2019 |
20/2019 |
|
||
TTF1 |
18/2019 |
little staining |
|
||
MNF116 |
16/2019 |
little staining |
|
||
CD45 |
0/2019 |
0/2019 |
10/1019 |
||
Lymphoid infiltrates: positive for CD45, negative for cytokeratins, TTF-1 and neuroendocrine markers.
inflammatory
lymphomas
Other neuroendocrine tumours
carcinoid tumours show a much lower mitotic count, less apoptosis and less necrosis. They show nuclear staining for the retinoblastoma protein2.
To distinguish small cell carcinoma from large cell neuroendocrine carcinoma, a cut off in nuclear size of three times the size of the nucleus of a lymphocyte has been proposed. However, a morphometric study showed a considerable overlap in this parameter11.
Other "small round blue cell tumours"
PNET: lower mitotic count, is also positive for CD998,10 but negative for TTF-1 and cytokeratins
metastatic Merkel cell carcinoma is positive for CK203,4 but negative for CK7 and TTF-14
Other primary and metastatic non-small cell carcinomas
Treatment is by chemotherapy9. Resection is appropriate for a few low stage tumours.
Widespread dissemination makes the TNM staging inappropriate and small cell carcinoma is staged as limited versus extensive disease. Adverse prognostic markers include extensive stage, poor performance status, elevated serum LDH or alkaline phosphatase and low plasma soduim.
Tumours of the Lung, Pleura, Thymus and Heart. WHO Classification of Tumours. IARC Press 2004.
9 Johnson DH Management of small cell lung cancer: current state of the art. Chest 1999; 116:525S-530S
This page last revised 31.1.2010.
©SMUHT/PW Bishop