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image/svg+xml Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Closed Access logo, derived from PLoS Open Access logo. This version with transparent background. http://commons.wikimedia.org/wiki/File:Closed_Access_logo_transparent.svg Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Onkologiearrow_drop_down
image/svg+xml Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Closed Access logo, derived from PLoS Open Access logo. This version with transparent background. http://commons.wikimedia.org/wiki/File:Closed_Access_logo_transparent.svg Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao
Onkologie
Article . 2009 . Peer-reviewed
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Testicular Intraepithelial Neoplasia: The Precursor of Testicular Germ Cell Tumors

Authors: K.-P. Dieckmann; V. Loy;

Testicular Intraepithelial Neoplasia: The Precursor of Testicular Germ Cell Tumors

Abstract

Testicular intraepithelial neoplasia (TIN; so-called carcinoma in situ of the testis) is the uniform precursor of testicular germ-cell tumors. TIN is derived from embryonal gonocytes and is present in the testis of a future testis cancer patient at the time of birth. TIN spreads inside the seminiferous tubules until it progresses to invasive cancer. Diagnosis is best achieved by surgical biopsy of the testis and subsequent im-munohistological staining of placental alkaline phosphatase. This enzyme is present in gonocytes, TIN, and seminoma as well as in several other types of germ-cell tumors but not in normal germ cells. TIN is found in testicular tissue adjacent to testicular germ-cell tumors and is observed in all clinical groups known to be at risk for testicular cancer: cryptorchidism (2-3%), infertility (1%), ambiguous genitalia (25%), in contralateral testis of patients with testis cancer (3-6%). Conversely, TIN is not found in the normal male population.If TIN is left untreated, there is a 50% probability of progressing to frank germ-cell neoplasm within 5 years. Localized radiotherapy to the testis with 18-20 Gy eradicates TIN and germ cells while Leydig cells are preserved. The patient can thus be spared orchiectomy and hormone supplementation. The concept of TIN offers the chance of very early detection of testis cancer and organ-preserving early treatment.

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selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
3
Average
Average
Average
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