A rare complication of ventriculoperitoneal shunt: Pleural effusion without intrathoracic ventriculoperitoneal shunt catheter
Symptomatic pleural effusion following ventriculoperitoneal shunt (VPS) insertion is very rare and poorly understood in the literature in contrary to other mechanical complications. We report a case of 15 month-year-old girl who had VP shunt for congenital hydrocephalus. Twelve months after surgery,...
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Veröffentlicht in: | Surgical neurology international 2020-09, Vol.11, p.291, Article 291 |
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creator | Hilmani, Said Mesbahi, Tarek Bouaggad, Abderrahman Lakhdar, Abdelhakim |
description | Symptomatic pleural effusion following ventriculoperitoneal shunt (VPS) insertion is very rare and poorly understood in the literature in contrary to other mechanical complications.
We report a case of 15 month-year-old girl who had VP shunt for congenital hydrocephalus. Twelve months after surgery, she was diagnosed with massive hydrothorax. Chest X-ray and thoracoabdominal CT scan confirmed the right pleurisy and showed the tip of the peritoneal catheter in the general peritoneal cavity. We made thoracic drainage of the transudative pleural effusion. When we released the chest tube, 24 h after, the girl showed a respiratory distress again and the effusion resumed at the X-ray control. Her symptoms abated after the realization of a ventriculoatrial shunt "VAS." Repeat chest X-ray confirmed the resolution of the hydrothorax.
Despite the not yet well-understood mechanism of this rare and important VPS complication, management is simple based on X-ray confirmation, thoracentesis with biological analysis, and catheter replacement, especially in atrium "VAS." |
doi_str_mv | 10.25259/SNI_57_2020 |
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We report a case of 15 month-year-old girl who had VP shunt for congenital hydrocephalus. Twelve months after surgery, she was diagnosed with massive hydrothorax. Chest X-ray and thoracoabdominal CT scan confirmed the right pleurisy and showed the tip of the peritoneal catheter in the general peritoneal cavity. We made thoracic drainage of the transudative pleural effusion. When we released the chest tube, 24 h after, the girl showed a respiratory distress again and the effusion resumed at the X-ray control. Her symptoms abated after the realization of a ventriculoatrial shunt "VAS." Repeat chest X-ray confirmed the resolution of the hydrothorax.
Despite the not yet well-understood mechanism of this rare and important VPS complication, management is simple based on X-ray confirmation, thoracentesis with biological analysis, and catheter replacement, especially in atrium "VAS."</description><identifier>ISSN: 2229-5097</identifier><identifier>ISSN: 2152-7806</identifier><identifier>EISSN: 2152-7806</identifier><identifier>DOI: 10.25259/SNI_57_2020</identifier><identifier>PMID: 33093968</identifier><language>eng</language><publisher>United States: Scientific Scholar</publisher><subject>Case Report</subject><ispartof>Surgical neurology international, 2020-09, Vol.11, p.291, Article 291</ispartof><rights>Copyright: © 2020 Surgical Neurology International.</rights><rights>Copyright: © 2020 Surgical Neurology International 2020</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c2660-f537618275bf6716499ed3445b1456afac33f5d09970deced6a5d73966de46ce3</citedby><cites>FETCH-LOGICAL-c2660-f537618275bf6716499ed3445b1456afac33f5d09970deced6a5d73966de46ce3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7568093/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7568093/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33093968$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hilmani, Said</creatorcontrib><creatorcontrib>Mesbahi, Tarek</creatorcontrib><creatorcontrib>Bouaggad, Abderrahman</creatorcontrib><creatorcontrib>Lakhdar, Abdelhakim</creatorcontrib><title>A rare complication of ventriculoperitoneal shunt: Pleural effusion without intrathoracic ventriculoperitoneal shunt catheter</title><title>Surgical neurology international</title><addtitle>Surg Neurol Int</addtitle><description>Symptomatic pleural effusion following ventriculoperitoneal shunt (VPS) insertion is very rare and poorly understood in the literature in contrary to other mechanical complications.
We report a case of 15 month-year-old girl who had VP shunt for congenital hydrocephalus. Twelve months after surgery, she was diagnosed with massive hydrothorax. Chest X-ray and thoracoabdominal CT scan confirmed the right pleurisy and showed the tip of the peritoneal catheter in the general peritoneal cavity. We made thoracic drainage of the transudative pleural effusion. When we released the chest tube, 24 h after, the girl showed a respiratory distress again and the effusion resumed at the X-ray control. Her symptoms abated after the realization of a ventriculoatrial shunt "VAS." Repeat chest X-ray confirmed the resolution of the hydrothorax.
Despite the not yet well-understood mechanism of this rare and important VPS complication, management is simple based on X-ray confirmation, thoracentesis with biological analysis, and catheter replacement, especially in atrium "VAS."</description><subject>Case Report</subject><issn>2229-5097</issn><issn>2152-7806</issn><issn>2152-7806</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNp9UUtLAzEQDqLYUnvzLPkBruaxSTYehCI-CkUF9RzSbOJGtpuS3a148L-bWi314lxmhvnm--YBwDFGZ4QRJs-f7qeKCUUQQXtgSDAjmSgQ308xITJjSIoBGLftG0pGKcZIHoIBpUhSyYsh-JzAqKOFJiyWtTe686GBwcGVbbroTV-HpY2-C43VNWyrvuku4GNt-5hS61zfrvHvvqtC30GfenQKozbe_EMBk05lOxuPwIHTdWvHP34EXm6un6_ustnD7fRqMssM4RxljlHBcUEEmzsuMM-ltCXNczbHOePaaUOpYyWSUqDSGltyzUqRFuSlzbmxdAQuN7zLfr6wpVlPpmu1jH6h44cK2qu_lcZX6jWslGC8SKdKBKcbAhND20brtr0Yqe9PqJ1PJPjJrt4W_Ht3-gX8V4mU</recordid><startdate>20200918</startdate><enddate>20200918</enddate><creator>Hilmani, Said</creator><creator>Mesbahi, Tarek</creator><creator>Bouaggad, Abderrahman</creator><creator>Lakhdar, Abdelhakim</creator><general>Scientific Scholar</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>5PM</scope></search><sort><creationdate>20200918</creationdate><title>A rare complication of ventriculoperitoneal shunt: Pleural effusion without intrathoracic ventriculoperitoneal shunt catheter</title><author>Hilmani, Said ; Mesbahi, Tarek ; Bouaggad, Abderrahman ; Lakhdar, Abdelhakim</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2660-f537618275bf6716499ed3445b1456afac33f5d09970deced6a5d73966de46ce3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Case Report</topic><toplevel>online_resources</toplevel><creatorcontrib>Hilmani, Said</creatorcontrib><creatorcontrib>Mesbahi, Tarek</creatorcontrib><creatorcontrib>Bouaggad, Abderrahman</creatorcontrib><creatorcontrib>Lakhdar, Abdelhakim</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Surgical neurology international</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hilmani, Said</au><au>Mesbahi, Tarek</au><au>Bouaggad, Abderrahman</au><au>Lakhdar, Abdelhakim</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A rare complication of ventriculoperitoneal shunt: Pleural effusion without intrathoracic ventriculoperitoneal shunt catheter</atitle><jtitle>Surgical neurology international</jtitle><addtitle>Surg Neurol Int</addtitle><date>2020-09-18</date><risdate>2020</risdate><volume>11</volume><spage>291</spage><pages>291-</pages><artnum>291</artnum><issn>2229-5097</issn><issn>2152-7806</issn><eissn>2152-7806</eissn><abstract>Symptomatic pleural effusion following ventriculoperitoneal shunt (VPS) insertion is very rare and poorly understood in the literature in contrary to other mechanical complications.
We report a case of 15 month-year-old girl who had VP shunt for congenital hydrocephalus. Twelve months after surgery, she was diagnosed with massive hydrothorax. Chest X-ray and thoracoabdominal CT scan confirmed the right pleurisy and showed the tip of the peritoneal catheter in the general peritoneal cavity. We made thoracic drainage of the transudative pleural effusion. When we released the chest tube, 24 h after, the girl showed a respiratory distress again and the effusion resumed at the X-ray control. Her symptoms abated after the realization of a ventriculoatrial shunt "VAS." Repeat chest X-ray confirmed the resolution of the hydrothorax.
Despite the not yet well-understood mechanism of this rare and important VPS complication, management is simple based on X-ray confirmation, thoracentesis with biological analysis, and catheter replacement, especially in atrium "VAS."</abstract><cop>United States</cop><pub>Scientific Scholar</pub><pmid>33093968</pmid><doi>10.25259/SNI_57_2020</doi><oa>free_for_read</oa></addata></record> |
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title | A rare complication of ventriculoperitoneal shunt: Pleural effusion without intrathoracic ventriculoperitoneal shunt catheter |
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