Bilaterally ectopic pelvic kidneys masquerading as horseshoe kidney in Fanconi anemia
Fanconi anemia (FA) is a genetic disease associated with the risk of different congenital malformations, bone marrow failure, and predisposition to cancer. Congenital abnormalities of the kidney and urinary tract are not infrequent in FA with renal ectopia being one of them. The incidence of the bil...
Gespeichert in:
Veröffentlicht in: | Journal of nuclear medicine technology 2022-02 |
---|---|
Hauptverfasser: | , , , , , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | |
---|---|
container_issue | |
container_start_page | |
container_title | Journal of nuclear medicine technology |
container_volume | |
creator | Tanigassalam, Sindhu Krishnaraju, Venkata Subramanian Sood, Ashwani Aggarwal, Piyush Bhattacharya, Anish Bansal, Deepak Roy, Pritam Singha |
description | Fanconi anemia (FA) is a genetic disease associated with the risk of different congenital malformations, bone marrow failure, and predisposition to cancer. Congenital abnormalities of the kidney and urinary tract are not infrequent in FA with renal ectopia being one of them. The incidence of the bilateral pelvic ectopic kidney is restricted to only a few reported cases; however, its association with FA has never been reported in the literature. We present a case of Fanconi anemia in a young girl with apparently fused kidneys on a
Tc-DMSA planar scan which was confirmed to be bilateral pelvic kidneys on hybrid cross-sectional imaging. |
doi_str_mv | 10.2967/jnmt.121.263543 |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_proquest_miscellaneous_2632809867</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2632809867</sourcerecordid><originalsourceid>FETCH-LOGICAL-p561-2384748a89c2988927d4f05b1b072d6998c4261d9f8a9a7357cfbc85db21705d3</originalsourceid><addsrcrecordid>eNo1kE1LwzAAhoMgbk7P3iRHL635aL6OOpwKAy_zXNIkdZlpWptW6L9fwXp6Lw8vDw8AdxjlRHHxeIrNkGOCc8IpK-gFWGNGWca4YCtwndIJIcwIkldgRRlWggi8Bp_PPujB9TqECToztJ03sHPhd55vb6ObEmx0-hlnxPr4BXWCx7ZPLh1btxDQR7jT0bTRQx1d4_UNuKx1SO522Q047F4O27ds__H6vn3aZx3jOCNUFqKQWipDlJSKCFvUiFW4QoJYrpQ0BeHYqlpqpQVlwtSVkcxWBAvELN2Ah7_brm9nwzSUjU_GhTBbtGMq5xBEIiW5mNH7BR2rxtmy632j-6n8L0HPAQ9elA</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2632809867</pqid></control><display><type>article</type><title>Bilaterally ectopic pelvic kidneys masquerading as horseshoe kidney in Fanconi anemia</title><source>EZB-FREE-00999 freely available EZB journals</source><source>Alma/SFX Local Collection</source><creator>Tanigassalam, Sindhu ; Krishnaraju, Venkata Subramanian ; Sood, Ashwani ; Aggarwal, Piyush ; Bhattacharya, Anish ; Bansal, Deepak ; Roy, Pritam Singha</creator><creatorcontrib>Tanigassalam, Sindhu ; Krishnaraju, Venkata Subramanian ; Sood, Ashwani ; Aggarwal, Piyush ; Bhattacharya, Anish ; Bansal, Deepak ; Roy, Pritam Singha</creatorcontrib><description>Fanconi anemia (FA) is a genetic disease associated with the risk of different congenital malformations, bone marrow failure, and predisposition to cancer. Congenital abnormalities of the kidney and urinary tract are not infrequent in FA with renal ectopia being one of them. The incidence of the bilateral pelvic ectopic kidney is restricted to only a few reported cases; however, its association with FA has never been reported in the literature. We present a case of Fanconi anemia in a young girl with apparently fused kidneys on a
Tc-DMSA planar scan which was confirmed to be bilateral pelvic kidneys on hybrid cross-sectional imaging.</description><identifier>EISSN: 1535-5675</identifier><identifier>DOI: 10.2967/jnmt.121.263543</identifier><identifier>PMID: 35197271</identifier><language>eng</language><publisher>United States</publisher><ispartof>Journal of nuclear medicine technology, 2022-02</ispartof><rights>Copyright © 2022 by the Society of Nuclear Medicine and Molecular Imaging, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35197271$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tanigassalam, Sindhu</creatorcontrib><creatorcontrib>Krishnaraju, Venkata Subramanian</creatorcontrib><creatorcontrib>Sood, Ashwani</creatorcontrib><creatorcontrib>Aggarwal, Piyush</creatorcontrib><creatorcontrib>Bhattacharya, Anish</creatorcontrib><creatorcontrib>Bansal, Deepak</creatorcontrib><creatorcontrib>Roy, Pritam Singha</creatorcontrib><title>Bilaterally ectopic pelvic kidneys masquerading as horseshoe kidney in Fanconi anemia</title><title>Journal of nuclear medicine technology</title><addtitle>J Nucl Med Technol</addtitle><description>Fanconi anemia (FA) is a genetic disease associated with the risk of different congenital malformations, bone marrow failure, and predisposition to cancer. Congenital abnormalities of the kidney and urinary tract are not infrequent in FA with renal ectopia being one of them. The incidence of the bilateral pelvic ectopic kidney is restricted to only a few reported cases; however, its association with FA has never been reported in the literature. We present a case of Fanconi anemia in a young girl with apparently fused kidneys on a
Tc-DMSA planar scan which was confirmed to be bilateral pelvic kidneys on hybrid cross-sectional imaging.</description><issn>1535-5675</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNo1kE1LwzAAhoMgbk7P3iRHL635aL6OOpwKAy_zXNIkdZlpWptW6L9fwXp6Lw8vDw8AdxjlRHHxeIrNkGOCc8IpK-gFWGNGWca4YCtwndIJIcwIkldgRRlWggi8Bp_PPujB9TqECToztJ03sHPhd55vb6ObEmx0-hlnxPr4BXWCx7ZPLh1btxDQR7jT0bTRQx1d4_UNuKx1SO522Q047F4O27ds__H6vn3aZx3jOCNUFqKQWipDlJSKCFvUiFW4QoJYrpQ0BeHYqlpqpQVlwtSVkcxWBAvELN2Ah7_brm9nwzSUjU_GhTBbtGMq5xBEIiW5mNH7BR2rxtmy632j-6n8L0HPAQ9elA</recordid><startdate>20220223</startdate><enddate>20220223</enddate><creator>Tanigassalam, Sindhu</creator><creator>Krishnaraju, Venkata Subramanian</creator><creator>Sood, Ashwani</creator><creator>Aggarwal, Piyush</creator><creator>Bhattacharya, Anish</creator><creator>Bansal, Deepak</creator><creator>Roy, Pritam Singha</creator><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>20220223</creationdate><title>Bilaterally ectopic pelvic kidneys masquerading as horseshoe kidney in Fanconi anemia</title><author>Tanigassalam, Sindhu ; Krishnaraju, Venkata Subramanian ; Sood, Ashwani ; Aggarwal, Piyush ; Bhattacharya, Anish ; Bansal, Deepak ; Roy, Pritam Singha</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p561-2384748a89c2988927d4f05b1b072d6998c4261d9f8a9a7357cfbc85db21705d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tanigassalam, Sindhu</creatorcontrib><creatorcontrib>Krishnaraju, Venkata Subramanian</creatorcontrib><creatorcontrib>Sood, Ashwani</creatorcontrib><creatorcontrib>Aggarwal, Piyush</creatorcontrib><creatorcontrib>Bhattacharya, Anish</creatorcontrib><creatorcontrib>Bansal, Deepak</creatorcontrib><creatorcontrib>Roy, Pritam Singha</creatorcontrib><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of nuclear medicine technology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tanigassalam, Sindhu</au><au>Krishnaraju, Venkata Subramanian</au><au>Sood, Ashwani</au><au>Aggarwal, Piyush</au><au>Bhattacharya, Anish</au><au>Bansal, Deepak</au><au>Roy, Pritam Singha</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Bilaterally ectopic pelvic kidneys masquerading as horseshoe kidney in Fanconi anemia</atitle><jtitle>Journal of nuclear medicine technology</jtitle><addtitle>J Nucl Med Technol</addtitle><date>2022-02-23</date><risdate>2022</risdate><eissn>1535-5675</eissn><abstract>Fanconi anemia (FA) is a genetic disease associated with the risk of different congenital malformations, bone marrow failure, and predisposition to cancer. Congenital abnormalities of the kidney and urinary tract are not infrequent in FA with renal ectopia being one of them. The incidence of the bilateral pelvic ectopic kidney is restricted to only a few reported cases; however, its association with FA has never been reported in the literature. We present a case of Fanconi anemia in a young girl with apparently fused kidneys on a
Tc-DMSA planar scan which was confirmed to be bilateral pelvic kidneys on hybrid cross-sectional imaging.</abstract><cop>United States</cop><pmid>35197271</pmid><doi>10.2967/jnmt.121.263543</doi></addata></record> |
fulltext | fulltext |
identifier | EISSN: 1535-5675 |
ispartof | Journal of nuclear medicine technology, 2022-02 |
issn | 1535-5675 |
language | eng |
recordid | cdi_proquest_miscellaneous_2632809867 |
source | EZB-FREE-00999 freely available EZB journals; Alma/SFX Local Collection |
title | Bilaterally ectopic pelvic kidneys masquerading as horseshoe kidney in Fanconi anemia |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-07T00%3A47%3A39IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Bilaterally%20ectopic%20pelvic%20kidneys%20masquerading%20as%20horseshoe%20kidney%20in%20Fanconi%20anemia&rft.jtitle=Journal%20of%20nuclear%20medicine%20technology&rft.au=Tanigassalam,%20Sindhu&rft.date=2022-02-23&rft.eissn=1535-5675&rft_id=info:doi/10.2967/jnmt.121.263543&rft_dat=%3Cproquest_pubme%3E2632809867%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2632809867&rft_id=info:pmid/35197271&rfr_iscdi=true |