View source for Template:Infobox - tumor/documentation

== An example ==
{{Infobox - tumor
| name = Brenner's tumor
| image = Brenner tumour intermed mag.jpg
| caption = Bright nests of cells of transitional epithelium character are surrounded by relatively abundant masses of mesenchymal origin
| ICD = {{ICD|D27}} (Benign), {{ICD|C56}} (malignant),  {{ICD|D39,1}} (borderline), {{ICD|D39,1}} (proliferating)
| ICD-O = {{ICDO|9000}}
| localization = [[ovary]]
| prevalence in the Czech Republic = 
| incidence in the Czech Republic = 
| maximum incidence = 50 years
| prognosis = 
| key mutation = 
| signalling cascade = 
| histological type = adenofibroma 
| part of a syndrome = [[Meigs syndrome]]
| positive immunohistochemical markers = [[Keratin (marker)|keratin]], [[EMA]], [[CEA]], [[Glycogen (marker)|glycogen]], [[Chromogranin]], [[NSE]] and [[EGFR]]
| negative immunohistochemical markers = [[p16]], [[p53]]
| molecular markers = 
| therapeutic modalities = 
}}

<pre style="width:55%; overflow:auto; margin-right:5px">
{{Infobox - tumor
| name = Brenner's tumor
| image = Brenner tumour intermed mag.jpg
| caption = Bright nests of cells of transitional epithelium character are surrounded by relatively abundant masses of mesenchymal origin
| ICD = {{ICD|D27}} (Benign), {{ICD|C56}} (malignant),  {{ICD|D39,1}} (borderline), {{ICD|D39,1}} (proliferating)
| ICD-O = {{ICDO|9000}}
| localization = [[ovary]]
| prevalence in the Czech Republic = 
| incidence in the Czech Republic = 
| maximum incidence = 50 years
| prognosis = 
| key mutation = 
| signalling cascade = 
| histological type = adenofibroma 
| part of a syndrome = [[Meigs syndrome]]
| positive immunohistochemical markers = [[Keratin (marker)|keratin]], [[EMA]], [[CEA]], [[Glycogen (marker)|glycogen]], [[Chromogranin]], [[NSE]] and [[EGFR]]
| negative immunohistochemical markers = [[p16]], [[p53]]
| molecular markers = 
| therapeutic modalities = 
}}
</pre>