Renal primitive neuroectodermal tumor with elevated plasma adrenocorticotropic hormone levels: A case report
INTRODUCTIONPrimitive neuroectodermal tumors are small round-cell tumors - Ewing sarcoma family, frequently occurring in the extremities, but rarely in the kidney. CASE PRESENTATIONA 58-year-old woman presented with whole-body edema and weakness of lower limb muscles. Computed tomography revealed a...
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| Veröffentlicht in: | IJU case reports 2019, Vol.2 (3), p.128-131 |
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| creator | Shimizu, Nobuaki Hasumi, Masaru Hamano, Tatsuya Iijima, Misa Yoshioka, Takako Yamazaki, Yuto Sasano, Hironobu |
| description | INTRODUCTIONPrimitive neuroectodermal tumors are small round-cell tumors - Ewing sarcoma family, frequently occurring in the extremities, but rarely in the kidney. CASE PRESENTATIONA 58-year-old woman presented with whole-body edema and weakness of lower limb muscles. Computed tomography revealed a left renal tumor, and the plasma adrenocorticotropic hormone level was elevated. The tumor was surgically removed without complications, her plasma adrenocorticotropic hormone reverted to normal levels, and symptoms disappeared after surgery. Histopathological examination revealed a primitive neuroectodermal tumor arising in her kidney. The patient was alive without metastasis 3 years after the surgery. CONCLUSIONWe report the first case of renal primitive neuroectodermal tumor accompanying elevated plasma adrenocorticotropic hormone levels which are thought to be produced and secreted in an ectopic fashion. |
| doi_str_mv | 10.1002/iju5.12057 |
| format | Report |
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CASE PRESENTATIONA 58-year-old woman presented with whole-body edema and weakness of lower limb muscles. Computed tomography revealed a left renal tumor, and the plasma adrenocorticotropic hormone level was elevated. The tumor was surgically removed without complications, her plasma adrenocorticotropic hormone reverted to normal levels, and symptoms disappeared after surgery. Histopathological examination revealed a primitive neuroectodermal tumor arising in her kidney. The patient was alive without metastasis 3 years after the surgery. CONCLUSIONWe report the first case of renal primitive neuroectodermal tumor accompanying elevated plasma adrenocorticotropic hormone levels which are thought to be produced and secreted in an ectopic fashion.</description><identifier>EISSN: 2577-171X</identifier><identifier>DOI: 10.1002/iju5.12057</identifier><language>eng</language><ispartof>IJU case reports, 2019, Vol.2 (3), p.128-131</ispartof><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>780,784,864,4490,27925</link.rule.ids></links><search><creatorcontrib>Shimizu, Nobuaki</creatorcontrib><creatorcontrib>Hasumi, Masaru</creatorcontrib><creatorcontrib>Hamano, Tatsuya</creatorcontrib><creatorcontrib>Iijima, Misa</creatorcontrib><creatorcontrib>Yoshioka, Takako</creatorcontrib><creatorcontrib>Yamazaki, Yuto</creatorcontrib><creatorcontrib>Sasano, Hironobu</creatorcontrib><title>Renal primitive neuroectodermal tumor with elevated plasma adrenocorticotropic hormone levels: A case report</title><title>IJU case reports</title><description>INTRODUCTIONPrimitive neuroectodermal tumors are small round-cell tumors - Ewing sarcoma family, frequently occurring in the extremities, but rarely in the kidney. CASE PRESENTATIONA 58-year-old woman presented with whole-body edema and weakness of lower limb muscles. Computed tomography revealed a left renal tumor, and the plasma adrenocorticotropic hormone level was elevated. The tumor was surgically removed without complications, her plasma adrenocorticotropic hormone reverted to normal levels, and symptoms disappeared after surgery. Histopathological examination revealed a primitive neuroectodermal tumor arising in her kidney. The patient was alive without metastasis 3 years after the surgery. CONCLUSIONWe report the first case of renal primitive neuroectodermal tumor accompanying elevated plasma adrenocorticotropic hormone levels which are thought to be produced and secreted in an ectopic fashion.</description><issn>2577-171X</issn><fulltext>true</fulltext><rsrctype>report</rsrctype><creationdate>2019</creationdate><recordtype>report</recordtype><recordid>eNqVyjFOAzEQQFErEhIRpOEEU9Ik2N7dLNAhBKJGKdJFlneiOLI9zowdrs8WXIDqF_8p9WD0xmhtn8K5DRtj9TAu1NIO47g2o9nfqpXIWc9Am27b26WK35hdhMIhhRquCBkbE_pKE3KaT22JGH5CPQFGvLqKE5ToJDlwE2MmT1yDp8pUgocTcaKMMFOM8gpv4J0gMJaZ3aubo4uCq7_eqcfPj93717owXRpKPaQgHmN0GanJwfad1i_P_dZ2_6C_8HhTMw</recordid><startdate>20190501</startdate><enddate>20190501</enddate><creator>Shimizu, Nobuaki</creator><creator>Hasumi, Masaru</creator><creator>Hamano, Tatsuya</creator><creator>Iijima, Misa</creator><creator>Yoshioka, Takako</creator><creator>Yamazaki, Yuto</creator><creator>Sasano, Hironobu</creator><scope>7X8</scope></search><sort><creationdate>20190501</creationdate><title>Renal primitive neuroectodermal tumor with elevated plasma adrenocorticotropic hormone levels: A case report</title><author>Shimizu, Nobuaki ; Hasumi, Masaru ; Hamano, Tatsuya ; Iijima, Misa ; Yoshioka, Takako ; Yamazaki, Yuto ; Sasano, Hironobu</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-proquest_miscellaneous_24300984623</frbrgroupid><rsrctype>reports</rsrctype><prefilter>reports</prefilter><language>eng</language><creationdate>2019</creationdate><toplevel>online_resources</toplevel><creatorcontrib>Shimizu, Nobuaki</creatorcontrib><creatorcontrib>Hasumi, Masaru</creatorcontrib><creatorcontrib>Hamano, Tatsuya</creatorcontrib><creatorcontrib>Iijima, Misa</creatorcontrib><creatorcontrib>Yoshioka, Takako</creatorcontrib><creatorcontrib>Yamazaki, Yuto</creatorcontrib><creatorcontrib>Sasano, Hironobu</creatorcontrib><collection>MEDLINE - Academic</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Shimizu, Nobuaki</au><au>Hasumi, Masaru</au><au>Hamano, Tatsuya</au><au>Iijima, Misa</au><au>Yoshioka, Takako</au><au>Yamazaki, Yuto</au><au>Sasano, Hironobu</au><format>book</format><genre>unknown</genre><ristype>RPRT</ristype><atitle>Renal primitive neuroectodermal tumor with elevated plasma adrenocorticotropic hormone levels: A case report</atitle><jtitle>IJU case reports</jtitle><date>2019-05-01</date><risdate>2019</risdate><volume>2</volume><issue>3</issue><spage>128</spage><epage>131</epage><pages>128-131</pages><eissn>2577-171X</eissn><abstract>INTRODUCTIONPrimitive neuroectodermal tumors are small round-cell tumors - Ewing sarcoma family, frequently occurring in the extremities, but rarely in the kidney. CASE PRESENTATIONA 58-year-old woman presented with whole-body edema and weakness of lower limb muscles. Computed tomography revealed a left renal tumor, and the plasma adrenocorticotropic hormone level was elevated. The tumor was surgically removed without complications, her plasma adrenocorticotropic hormone reverted to normal levels, and symptoms disappeared after surgery. Histopathological examination revealed a primitive neuroectodermal tumor arising in her kidney. The patient was alive without metastasis 3 years after the surgery. CONCLUSIONWe report the first case of renal primitive neuroectodermal tumor accompanying elevated plasma adrenocorticotropic hormone levels which are thought to be produced and secreted in an ectopic fashion.</abstract><doi>10.1002/iju5.12057</doi></addata></record> |
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| title | Renal primitive neuroectodermal tumor with elevated plasma adrenocorticotropic hormone levels: A case report |
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