| Literature DB >> 22844601 |
Rodolfo Montironi1, Antonio Lopez Beltran, Roberta Mazzucchelli, Liang Cheng, Marina Scarpelli.
Abstract
A problem when handling radical prostatectomy specimens (RPS) is that cancer is often not visible at gross examination, and the tumor extent is always underestimated by the naked eye. The challenge is increased further by the fact that prostate cancer is a notoriously multifocal and heterogeneous tumor. For the pathologist, the safest method to avoid undersampling of cancer is evidently that the entire prostate is submitted. Even though whole mounts of sections from RPS appear not to be superior to sections from standard blocks in detecting adverse pathological features, their use has the great advantage of displaying the architecture of the prostate and the identification and location of tumour nodules more clearly, with particular reference to the index tumour; further, it is easier to compare the pathological findings with those obtained from digital rectal examination (DRE), transrectal ultrasound (TRUS), and prostate biopsies. We are in favour of complete sampling of the RPS examined with the whole mount technique. There are reasons in favour and a few drawbacks. Its implementation does not require an additional amount of work from the technicians' side. It gives further clinical significance to our work of uropathologists.Entities:
Year: 2012 PMID: 22844601 PMCID: PMC3400332 DOI: 10.1155/2012/932784
Source DB: PubMed Journal: Int J Breast Cancer ISSN: 2090-3189
Figure 1Complete sampling with the whole-mount technique of a prostate specimen. Hematoxylin and eosin-stained sections of prostate specimen are shown on the left and the corresponding mapping on the right. The dotted areas on the slides and the black areas of the map represent two prostatic cancer foci, the index tumour being present on the left of the slides. Extraprostatic extension (EPE) and positive surgical margin (SM+) are present in the posterolateral aspect of the body of the prostate and in one of the slides of the base (see details in the separate images) (SV: seminal vesicles).
Comparison between Dr. Vainer et al.'s study [8] and Ancona experience [3].
| Features | Dr. Vainer et al.'s study | Ancona experience |
|---|---|---|
| Prostate weight and size (and volume) | Yes | Yes |
| Fixation enhancement | Separating the two lobes | Formalin injection |
| Inking of the surface | Two colours, anterior, and posterior halves | One colour; orientation with a cut on the right |
| Presectioning fixation (time) | Acid formic (20 h) and 4% buffered formalin (24 h) | 4% buffered formalin (24 h) |
| Sectioning interval | Approximately 3 mm (Apex and base: 5–10 mm) | 3 mm (Apex and base: 3 mm) |
| Subdivision of the slices of the prostate body | Yes, to fit standard cassettes | No (whole mounts) |
| Seminal vesicles | As a minimum the apex and a cross-section | Sandwich method (all included) |
| Postsectioning fixation (time) | 4% buffered formalin (not mentioned) | 4% buffered formalin (24 h) |
| No. of cassettes/total slides (% examined) | 18–76 (70%) | 9–14 (100%) |
| Processing | Not mentioned | As for regular size cassettes |
| Slide size (section thickness) | 7.5 cm by 2.5 cm (4 | 7.5 cm by 5.0 cm (5 |
| Slide staining procedure | Not mentioned | Manual |