Register for email alerts and news feeds:
This journal | BMJ Group
rss
Published Online First: 19 December 2008. doi:10.1136/jcp.2008.063834
Journal of Clinical Pathology 2009;62:289
Copyright © 2009 by the BMJ Publishing Group Ltd & Association of Clinical Pathologists.

COMMENTARY

Stromal tumours: which diagnostic approach?

G Bevilacqua

Chairman, European Group for Molecular Pathology, ESP (European Society of Pathology); Director, Division of Surgical, Molecular and Ultrastructural Pathology, University of Pisa

G Bevilacqua, Division of Surgical, Molecular and Ultrastructural Pathology, University of Pisa, Italy; g.bevilacqua@med.unipi.it

Accepted 10 December 2008

The first 150 words of the full text of this article appear below.

Probably all pathologists agree that proliferations of stromal cells represent a somewhat complex chapter of pathology. In fact, their classification is still tentative, full of synonyms and with confusing terms, such as "inflammatory tumour" or "pseudosarcomatous proliferation".

Several factors can contribute to this complexity: a possible common progenitor (fibrocyte)1 for fibroblasts and myofibroblasts; the fact that the fibrocyte can be considered as belonging to the leucocytes; the possible epithelial origin of mesenchymal cells (epithelial–mesenchymal transition); and the interconnections between physiological and pathological stromal proliferations.2

The absence of a satisfactory classification provided by a rational base and of biological and clinical significance has negative consequences for the correct diagnosis of these diseases. The complex biology of stromal cells well explains the fact that immunohistochemistry gives contradictory results, often adding more confusion to a per se unclear morphological pattern.

Fortunately, molecular pathology is also entering into this field, thanks to our understanding . . . [Full text of this article]


Add to CiteULike CiteULike   Add to Complore Complore   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati    What's this?

Relevant Article

Would a morphomolecular approach help in defining pseudosarcomatous myofibroblastic proliferations? A study of a heart polypoid lesion
S Nemolato, T Dettori, P Caria, D V Frau, G Faa, R Vanni
J. Clin. Pathol. 2009 62: 377-379. [Abstract] [Full Text] [PDF]

This Article

Services
Citing Articles
Google Scholar
PubMed
Topic Collections
Bookmark with

Register for free content

The full back archive is now available for all BMJ Journals. Institutional subscribers may access the entire archive as part of their subscription. Personal subscribers will also have access to all content when logged in. Non-subscribers who register have free access to all articles published before 2006 right back to volume 1 issue 1. Register here to access the free archive of all BMJ Journals.

Don't forget to sign up for content alerts so you keep up to date with all the articles as they are published.

Pathology jobs

Pathology jobs