Incidental Finding of Autosomal Dominant Polycystic Kidney Disease With Liver Involvement on Tc-99m Sestamibi Scintigraphy
Autosomal dominant polycystic kidney disease is a systemic hereditary disease characterized by renal cysts and sometimes involvement of the liver. We present a 65-year-old woman with autosomal dominant polycystic kidney disease on regularly hemodialysis who recently experienced intermittent right up...
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Veröffentlicht in: | Clinical nuclear medicine 2011-07, Vol.36 (7), p.e69-e70 |
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description | Autosomal dominant polycystic kidney disease is a systemic hereditary disease characterized by renal cysts and sometimes involvement of the liver. We present a 65-year-old woman with autosomal dominant polycystic kidney disease on regularly hemodialysis who recently experienced intermittent right upper quadrant abdominal pain and elevated intact parathyroid hormone for more than a year. She was referred for double-phase Tc-99m sestamibi scintigraphy, under the impression of hyperparathyroidism. Apart form increased uptake in the right thyroid bed, the images showed a large photon-deficient area in the upper portion of the abdomen corresponding to the liver. |
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We present a 65-year-old woman with autosomal dominant polycystic kidney disease on regularly hemodialysis who recently experienced intermittent right upper quadrant abdominal pain and elevated intact parathyroid hormone for more than a year. She was referred for double-phase Tc-99m sestamibi scintigraphy, under the impression of hyperparathyroidism. Apart form increased uptake in the right thyroid bed, the images showed a large photon-deficient area in the upper portion of the abdomen corresponding to the liver.</description><identifier>ISSN: 0363-9762</identifier><identifier>EISSN: 1536-0229</identifier><identifier>DOI: 10.1097/RLU.0b013e318219ad4b</identifier><identifier>PMID: 21637047</identifier><language>eng</language><publisher>United States: Lippincott Williams & Wilkins, Inc</publisher><subject>Abdomen - diagnostic imaging ; Aged ; Female ; Humans ; Incidental Findings ; Liver - diagnostic imaging ; Polycystic Kidney, Autosomal Dominant - diagnostic imaging ; Radionuclide Imaging ; Technetium Tc 99m Sestamibi ; Ultrasonography</subject><ispartof>Clinical nuclear medicine, 2011-07, Vol.36 (7), p.e69-e70</ispartof><rights>2011 Lippincott Williams & Wilkins, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c3006-e17e10ae8462f21c7f43fc528f8d3861fba9cc406c16ed87f097147c81375cc53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21637047$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chang, Chih-Yung</creatorcontrib><creatorcontrib>Lin, Ko-Han</creatorcontrib><creatorcontrib>Chu, Yum-Kung</creatorcontrib><creatorcontrib>Chang, Cheng-Pei</creatorcontrib><creatorcontrib>Liu, Ren-Shyan</creatorcontrib><creatorcontrib>Wang, Shih-Jen</creatorcontrib><title>Incidental Finding of Autosomal Dominant Polycystic Kidney Disease With Liver Involvement on Tc-99m Sestamibi Scintigraphy</title><title>Clinical nuclear medicine</title><addtitle>Clin Nucl Med</addtitle><description>Autosomal dominant polycystic kidney disease is a systemic hereditary disease characterized by renal cysts and sometimes involvement of the liver. We present a 65-year-old woman with autosomal dominant polycystic kidney disease on regularly hemodialysis who recently experienced intermittent right upper quadrant abdominal pain and elevated intact parathyroid hormone for more than a year. She was referred for double-phase Tc-99m sestamibi scintigraphy, under the impression of hyperparathyroidism. Apart form increased uptake in the right thyroid bed, the images showed a large photon-deficient area in the upper portion of the abdomen corresponding to the liver.</description><subject>Abdomen - diagnostic imaging</subject><subject>Aged</subject><subject>Female</subject><subject>Humans</subject><subject>Incidental Findings</subject><subject>Liver - diagnostic imaging</subject><subject>Polycystic Kidney, Autosomal Dominant - diagnostic imaging</subject><subject>Radionuclide Imaging</subject><subject>Technetium Tc 99m Sestamibi</subject><subject>Ultrasonography</subject><issn>0363-9762</issn><issn>1536-0229</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkFtv1DAQhS0EotuWf4CQ33hKmbETO3msWgorVgL1Ih4jx5l0DYm9xMlW4dfXVS9IzMtojs6cGX2MvUc4Qaj0p8vNzQk0gJIklgIr0-bNK7bCQqoMhKhesxVIJbNKK3HADmP8BYAKVf6WHQhUUkOuV-zv2lvXkp9Mzy-cb52_5aHjp_MUYhiSeB4G542f-I_QL3aJk7P8m2s9LfzcRTKR-E83bfnG7Wnka78P_Z6GFMiD59c2q6qBX1GczOAax6-s85O7Hc1uuxyzN53pI7176kfs5uLz9dnXbPP9y_rsdJNZCaAyQk0IhspciU6g1V0uO1uIsitbWSrsGlNZm4OyqKgtdZfgYK5tiVIX1hbyiH18zN2N4c-cXqkHFy31vfEU5liXGkSVywKTM3902jHEOFJX70Y3mHGpEeoH6HWCXv8PPa19eDowNwO1L0vPlP_l3oV-ojH-7uc7GustmX7a1pBKghaZAETQacoeFCXvAUz0j0M</recordid><startdate>201107</startdate><enddate>201107</enddate><creator>Chang, Chih-Yung</creator><creator>Lin, Ko-Han</creator><creator>Chu, Yum-Kung</creator><creator>Chang, Cheng-Pei</creator><creator>Liu, Ren-Shyan</creator><creator>Wang, Shih-Jen</creator><general>Lippincott Williams & Wilkins, Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>201107</creationdate><title>Incidental Finding of Autosomal Dominant Polycystic Kidney Disease With Liver Involvement on Tc-99m Sestamibi Scintigraphy</title><author>Chang, Chih-Yung ; Lin, Ko-Han ; Chu, Yum-Kung ; Chang, Cheng-Pei ; Liu, Ren-Shyan ; Wang, Shih-Jen</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3006-e17e10ae8462f21c7f43fc528f8d3861fba9cc406c16ed87f097147c81375cc53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Abdomen - diagnostic imaging</topic><topic>Aged</topic><topic>Female</topic><topic>Humans</topic><topic>Incidental Findings</topic><topic>Liver - diagnostic imaging</topic><topic>Polycystic Kidney, Autosomal Dominant - diagnostic imaging</topic><topic>Radionuclide Imaging</topic><topic>Technetium Tc 99m Sestamibi</topic><topic>Ultrasonography</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chang, Chih-Yung</creatorcontrib><creatorcontrib>Lin, Ko-Han</creatorcontrib><creatorcontrib>Chu, Yum-Kung</creatorcontrib><creatorcontrib>Chang, Cheng-Pei</creatorcontrib><creatorcontrib>Liu, Ren-Shyan</creatorcontrib><creatorcontrib>Wang, Shih-Jen</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Clinical nuclear medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chang, Chih-Yung</au><au>Lin, Ko-Han</au><au>Chu, Yum-Kung</au><au>Chang, Cheng-Pei</au><au>Liu, Ren-Shyan</au><au>Wang, Shih-Jen</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Incidental Finding of Autosomal Dominant Polycystic Kidney Disease With Liver Involvement on Tc-99m Sestamibi Scintigraphy</atitle><jtitle>Clinical nuclear medicine</jtitle><addtitle>Clin Nucl Med</addtitle><date>2011-07</date><risdate>2011</risdate><volume>36</volume><issue>7</issue><spage>e69</spage><epage>e70</epage><pages>e69-e70</pages><issn>0363-9762</issn><eissn>1536-0229</eissn><abstract>Autosomal dominant polycystic kidney disease is a systemic hereditary disease characterized by renal cysts and sometimes involvement of the liver. We present a 65-year-old woman with autosomal dominant polycystic kidney disease on regularly hemodialysis who recently experienced intermittent right upper quadrant abdominal pain and elevated intact parathyroid hormone for more than a year. She was referred for double-phase Tc-99m sestamibi scintigraphy, under the impression of hyperparathyroidism. Apart form increased uptake in the right thyroid bed, the images showed a large photon-deficient area in the upper portion of the abdomen corresponding to the liver.</abstract><cop>United States</cop><pub>Lippincott Williams & Wilkins, Inc</pub><pmid>21637047</pmid><doi>10.1097/RLU.0b013e318219ad4b</doi></addata></record> |
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subjects | Abdomen - diagnostic imaging Aged Female Humans Incidental Findings Liver - diagnostic imaging Polycystic Kidney, Autosomal Dominant - diagnostic imaging Radionuclide Imaging Technetium Tc 99m Sestamibi Ultrasonography |
title | Incidental Finding of Autosomal Dominant Polycystic Kidney Disease With Liver Involvement on Tc-99m Sestamibi Scintigraphy |
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