| Unusual double primary neoplasia: adrenocortical and ureteral carcinomas in werner syndrome. | |
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MedLine Citation:
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PMID: 14963361 Owner: NLM Status: MEDLINE |
Abstract/OtherAbstract:
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Adrenocortical and ureteral carcinomas were observed in a 50-year-old Japanese woman with Werner syndrome (MIM No. 27770). The syndrome is an autosomal recessive disorder characterized by premature aging and an increased risk of rare cancers, which are often multiple. This is the first reported association of adrenocortical carcinoma in Werner syndrome. |
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Authors:
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Ryoji Takazawa; Junichi Ajima; Akimasa Yamauchi; Makoto Goto |
Publication Detail:
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Type: Case Reports; Journal Article |
Journal Detail:
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Title: Urologia internationalis Volume: 72 ISSN: 0042-1138 ISO Abbreviation: Urol. Int. Publication Date: 2004 |
Date Detail:
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Created Date: 2004-02-13 Completed Date: 2004-08-03 Revised Date: 2006-10-30 |
Medline Journal Info:
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Nlm Unique ID: 0417373 Medline TA: Urol Int Country: Switzerland |
Other Details:
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Languages: eng Pagination: 168-70 Citation Subset: IM |
Copyright Information:
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Copyright 2004 S. Karger AG, Basel |
Affiliation:
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Department of Urology, Tokyo Metropolitan Otsuka Hospital, Tokyo, Japan. |
Export Citation:
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| MeSH Terms | |
Descriptor/Qualifier:
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Adrenal Gland Neoplasms
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diagnosis* Adrenocortical Carcinoma / diagnosis* Carcinoma, Transitional Cell / diagnosis* Fatal Outcome Female Humans Middle Aged Neoplasms, Multiple Primary / diagnosis* Tomography, X-Ray Computed Ureteral Neoplasms / diagnosis* |
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
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