Spontaneous Hemothorax Complicating von Recklinghausen Disease: Case Report and Treatment Algorithm
Neurofibromatosis type 1 (NF1) is generally a benign disease but has the potential for rare and fatal complications. Vascular signs and symptoms associated with NF1 are reported in only 1–3% of patients. Pulmonary complications have been rarely described in the literature and spontaneous rupture of...
Gespeichert in:
Veröffentlicht in: | The Journal of emergency medicine 2020-02, Vol.58 (2), p.e63-e66 |
---|---|
Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | e66 |
---|---|
container_issue | 2 |
container_start_page | e63 |
container_title | The Journal of emergency medicine |
container_volume | 58 |
creator | Pantazopoulos, Ioannis Papazoglou, Georgios Strataki, Kalliopi Chalkias, Athanasios |
description | Neurofibromatosis type 1 (NF1) is generally a benign disease but has the potential for rare and fatal complications. Vascular signs and symptoms associated with NF1 are reported in only 1–3% of patients. Pulmonary complications have been rarely described in the literature and spontaneous rupture of a major thoracic artery is, however, extremely uncommon.
We report the case of a patient with NF1 admitted to the emergency department for the management of a spontaneous life-threatening left hemothorax. The patient became hemodynamically unstable after thoracic drainage. Computed tomography angiography revealed extravasation at the level of the eighth intercostal artery. Digital angiography showed an intercostal aneurysm. Catheterization of the eighth intercostal artery was unsuccessful and an open surgery was finally performed.
We highlight the importance of recognizing that patients with a benign disease like NF1 may present to the emergency department with a spontaneous life-threatening hemothorax. Immediate transfer for embolization is not always the best treatment management but thoracotomy is preferred in unstable patients. |
doi_str_mv | 10.1016/j.jemermed.2019.10.012 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2320641751</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0736467919308455</els_id><sourcerecordid>2320641751</sourcerecordid><originalsourceid>FETCH-LOGICAL-c434t-30b4e5041f1cd6ed4f6c1734e94557de3384742db60f22bf7666da4b587103803</originalsourceid><addsrcrecordid>eNqFkE1PIzEMhiPECsrHX0A5cpmSr0mmnEBlF5CQkHbZc5RJPDRlZjIkKWL__aYqPXOx5devbflB6IKSOSVUXq3naxggDuDmjNBFEeeEsgM0Y7xmVU3Y4hDNiOKyElItjtFJSmtCqCINPULHnKpGcSVmyP6ZwpjNCGGT8AMMIa9CNJ94GYap99ZkP77ijzDi32Df-lKszCbBiO98ApPgGi9LLM0pxIzN6PBLBJMHGDO-7V9D9Hk1nKEfnekTnH_lU_T318-X5UP19Hz_uLx9qqzgIlectAJqImhHrZPgRCctVVzAQtS1csB5I5RgrpWkY6ztlJTSGdHWjaKEN4Sfosvd3imG9w2krAefLPT97j3NOCNSUFXTYpU7q40hpQidnqIfTPynKdFbwHqt94D1FvBWL4DL4MXXjU277e3H9kSL4WZngPLph4eok_UwWnA-gs3aBf_djf__WpBF</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2320641751</pqid></control><display><type>article</type><title>Spontaneous Hemothorax Complicating von Recklinghausen Disease: Case Report and Treatment Algorithm</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals</source><creator>Pantazopoulos, Ioannis ; Papazoglou, Georgios ; Strataki, Kalliopi ; Chalkias, Athanasios</creator><creatorcontrib>Pantazopoulos, Ioannis ; Papazoglou, Georgios ; Strataki, Kalliopi ; Chalkias, Athanasios</creatorcontrib><description>Neurofibromatosis type 1 (NF1) is generally a benign disease but has the potential for rare and fatal complications. Vascular signs and symptoms associated with NF1 are reported in only 1–3% of patients. Pulmonary complications have been rarely described in the literature and spontaneous rupture of a major thoracic artery is, however, extremely uncommon.
We report the case of a patient with NF1 admitted to the emergency department for the management of a spontaneous life-threatening left hemothorax. The patient became hemodynamically unstable after thoracic drainage. Computed tomography angiography revealed extravasation at the level of the eighth intercostal artery. Digital angiography showed an intercostal aneurysm. Catheterization of the eighth intercostal artery was unsuccessful and an open surgery was finally performed.
We highlight the importance of recognizing that patients with a benign disease like NF1 may present to the emergency department with a spontaneous life-threatening hemothorax. Immediate transfer for embolization is not always the best treatment management but thoracotomy is preferred in unstable patients.</description><identifier>ISSN: 0736-4679</identifier><identifier>EISSN: 2352-5029</identifier><identifier>DOI: 10.1016/j.jemermed.2019.10.012</identifier><identifier>PMID: 31787374</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Computed Tomography Angiography ; hemothorax ; Hemothorax - diagnostic imaging ; Hemothorax - etiology ; Hemothorax - surgery ; Humans ; Male ; Middle Aged ; neurofibromatosis ; Neurofibromatosis 1 - complications ; thoracotomy ; von Recklinghausen disease</subject><ispartof>The Journal of emergency medicine, 2020-02, Vol.58 (2), p.e63-e66</ispartof><rights>2019 Elsevier Inc.</rights><rights>Copyright © 2019 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c434t-30b4e5041f1cd6ed4f6c1734e94557de3384742db60f22bf7666da4b587103803</citedby><cites>FETCH-LOGICAL-c434t-30b4e5041f1cd6ed4f6c1734e94557de3384742db60f22bf7666da4b587103803</cites><orcidid>0000-0002-8846-519X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.jemermed.2019.10.012$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,777,781,3537,27905,27906,45976</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31787374$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Pantazopoulos, Ioannis</creatorcontrib><creatorcontrib>Papazoglou, Georgios</creatorcontrib><creatorcontrib>Strataki, Kalliopi</creatorcontrib><creatorcontrib>Chalkias, Athanasios</creatorcontrib><title>Spontaneous Hemothorax Complicating von Recklinghausen Disease: Case Report and Treatment Algorithm</title><title>The Journal of emergency medicine</title><addtitle>J Emerg Med</addtitle><description>Neurofibromatosis type 1 (NF1) is generally a benign disease but has the potential for rare and fatal complications. Vascular signs and symptoms associated with NF1 are reported in only 1–3% of patients. Pulmonary complications have been rarely described in the literature and spontaneous rupture of a major thoracic artery is, however, extremely uncommon.
We report the case of a patient with NF1 admitted to the emergency department for the management of a spontaneous life-threatening left hemothorax. The patient became hemodynamically unstable after thoracic drainage. Computed tomography angiography revealed extravasation at the level of the eighth intercostal artery. Digital angiography showed an intercostal aneurysm. Catheterization of the eighth intercostal artery was unsuccessful and an open surgery was finally performed.
We highlight the importance of recognizing that patients with a benign disease like NF1 may present to the emergency department with a spontaneous life-threatening hemothorax. Immediate transfer for embolization is not always the best treatment management but thoracotomy is preferred in unstable patients.</description><subject>Computed Tomography Angiography</subject><subject>hemothorax</subject><subject>Hemothorax - diagnostic imaging</subject><subject>Hemothorax - etiology</subject><subject>Hemothorax - surgery</subject><subject>Humans</subject><subject>Male</subject><subject>Middle Aged</subject><subject>neurofibromatosis</subject><subject>Neurofibromatosis 1 - complications</subject><subject>thoracotomy</subject><subject>von Recklinghausen disease</subject><issn>0736-4679</issn><issn>2352-5029</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkE1PIzEMhiPECsrHX0A5cpmSr0mmnEBlF5CQkHbZc5RJPDRlZjIkKWL__aYqPXOx5devbflB6IKSOSVUXq3naxggDuDmjNBFEeeEsgM0Y7xmVU3Y4hDNiOKyElItjtFJSmtCqCINPULHnKpGcSVmyP6ZwpjNCGGT8AMMIa9CNJ94GYap99ZkP77ijzDi32Df-lKszCbBiO98ApPgGi9LLM0pxIzN6PBLBJMHGDO-7V9D9Hk1nKEfnekTnH_lU_T318-X5UP19Hz_uLx9qqzgIlectAJqImhHrZPgRCctVVzAQtS1csB5I5RgrpWkY6ztlJTSGdHWjaKEN4Sfosvd3imG9w2krAefLPT97j3NOCNSUFXTYpU7q40hpQidnqIfTPynKdFbwHqt94D1FvBWL4DL4MXXjU277e3H9kSL4WZngPLph4eok_UwWnA-gs3aBf_djf__WpBF</recordid><startdate>202002</startdate><enddate>202002</enddate><creator>Pantazopoulos, Ioannis</creator><creator>Papazoglou, Georgios</creator><creator>Strataki, Kalliopi</creator><creator>Chalkias, Athanasios</creator><general>Elsevier 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><orcidid>https://orcid.org/0000-0002-8846-519X</orcidid></search><sort><creationdate>202002</creationdate><title>Spontaneous Hemothorax Complicating von Recklinghausen Disease: Case Report and Treatment Algorithm</title><author>Pantazopoulos, Ioannis ; Papazoglou, Georgios ; Strataki, Kalliopi ; Chalkias, Athanasios</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c434t-30b4e5041f1cd6ed4f6c1734e94557de3384742db60f22bf7666da4b587103803</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Computed Tomography Angiography</topic><topic>hemothorax</topic><topic>Hemothorax - diagnostic imaging</topic><topic>Hemothorax - etiology</topic><topic>Hemothorax - surgery</topic><topic>Humans</topic><topic>Male</topic><topic>Middle Aged</topic><topic>neurofibromatosis</topic><topic>Neurofibromatosis 1 - complications</topic><topic>thoracotomy</topic><topic>von Recklinghausen disease</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pantazopoulos, Ioannis</creatorcontrib><creatorcontrib>Papazoglou, Georgios</creatorcontrib><creatorcontrib>Strataki, Kalliopi</creatorcontrib><creatorcontrib>Chalkias, Athanasios</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>The Journal of emergency medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pantazopoulos, Ioannis</au><au>Papazoglou, Georgios</au><au>Strataki, Kalliopi</au><au>Chalkias, Athanasios</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Spontaneous Hemothorax Complicating von Recklinghausen Disease: Case Report and Treatment Algorithm</atitle><jtitle>The Journal of emergency medicine</jtitle><addtitle>J Emerg Med</addtitle><date>2020-02</date><risdate>2020</risdate><volume>58</volume><issue>2</issue><spage>e63</spage><epage>e66</epage><pages>e63-e66</pages><issn>0736-4679</issn><eissn>2352-5029</eissn><abstract>Neurofibromatosis type 1 (NF1) is generally a benign disease but has the potential for rare and fatal complications. Vascular signs and symptoms associated with NF1 are reported in only 1–3% of patients. Pulmonary complications have been rarely described in the literature and spontaneous rupture of a major thoracic artery is, however, extremely uncommon.
We report the case of a patient with NF1 admitted to the emergency department for the management of a spontaneous life-threatening left hemothorax. The patient became hemodynamically unstable after thoracic drainage. Computed tomography angiography revealed extravasation at the level of the eighth intercostal artery. Digital angiography showed an intercostal aneurysm. Catheterization of the eighth intercostal artery was unsuccessful and an open surgery was finally performed.
We highlight the importance of recognizing that patients with a benign disease like NF1 may present to the emergency department with a spontaneous life-threatening hemothorax. Immediate transfer for embolization is not always the best treatment management but thoracotomy is preferred in unstable patients.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>31787374</pmid><doi>10.1016/j.jemermed.2019.10.012</doi><orcidid>https://orcid.org/0000-0002-8846-519X</orcidid></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0736-4679 |
ispartof | The Journal of emergency medicine, 2020-02, Vol.58 (2), p.e63-e66 |
issn | 0736-4679 2352-5029 |
language | eng |
recordid | cdi_proquest_miscellaneous_2320641751 |
source | MEDLINE; Elsevier ScienceDirect Journals |
subjects | Computed Tomography Angiography hemothorax Hemothorax - diagnostic imaging Hemothorax - etiology Hemothorax - surgery Humans Male Middle Aged neurofibromatosis Neurofibromatosis 1 - complications thoracotomy von Recklinghausen disease |
title | Spontaneous Hemothorax Complicating von Recklinghausen Disease: Case Report and Treatment Algorithm |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-19T01%3A12%3A34IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Spontaneous%20Hemothorax%20Complicating%20von%20Recklinghausen%20Disease:%20Case%20Report%20and%20Treatment%20Algorithm&rft.jtitle=The%20Journal%20of%20emergency%20medicine&rft.au=Pantazopoulos,%20Ioannis&rft.date=2020-02&rft.volume=58&rft.issue=2&rft.spage=e63&rft.epage=e66&rft.pages=e63-e66&rft.issn=0736-4679&rft.eissn=2352-5029&rft_id=info:doi/10.1016/j.jemermed.2019.10.012&rft_dat=%3Cproquest_cross%3E2320641751%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2320641751&rft_id=info:pmid/31787374&rft_els_id=S0736467919308455&rfr_iscdi=true |