A Case of Bilateral Congenital Pseudoarthrosis of Clavicle: An Uncommon Variant of a Rare Disorder
Congenital pseudarthrosis of the clavicle (CPC) is a rare disorder diagnosed at birth or early childhood presenting with a painless, non-tender mass on the clavicle. Its etiology is unknown, caused by failure of fusion of the medial and lateral ossification centers of the clavicle. Left-sided CPC is...
Gespeichert in:
Veröffentlicht in: | Curēus (Palo Alto, CA) CA), 2024-08, Vol.16 (8), p.e66594 |
---|---|
Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | |
---|---|
container_issue | 8 |
container_start_page | e66594 |
container_title | Curēus (Palo Alto, CA) |
container_volume | 16 |
creator | Boeisa, Ahmad N Alshammary, Alya A Albunyan, Sara AlMudayris, Lina AlSaeed, Mohammed |
description | Congenital pseudarthrosis of the clavicle (CPC) is a rare disorder diagnosed at birth or early childhood presenting with a painless, non-tender mass on the clavicle. Its etiology is unknown, caused by failure of fusion of the medial and lateral ossification centers of the clavicle. Left-sided CPC is rare and linked to other pathological abnormalities. Bilateral involvement is extremely rare and it is seen in association with other congenital malformations. A full-term newborn baby girl was examined after a complicated emergency cesarean section delivery. Upon initial pediatric examination, there was suspicion of bilateral clavicle fracture with no limitation of movement and equal moro reflex bilateral. Plain radiographs of the clavicle revealed a suspected bilateral fracture of the clavicle. At the two-month follow-up, X-rays were taken to assess the clavicle fractures showing persistent bilateral clavicle deformities and there was no interval callus formation which confirmed the diagnosis of bilateral CPC and excluded the presence of the fracture. Bilateral pseudarthrosis of the clavicle is a rare entity, and surgical correction is not required unless the patient develops symptoms of limitations of movement or for aesthetic causes. |
doi_str_mv | 10.7759/cureus.66594 |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_11383427</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>3102472029</sourcerecordid><originalsourceid>FETCH-LOGICAL-c300t-bbe1a83eee6a65f0abfbc755abb2e149eedcdf9dd5ac84c394e693b8c28470e53</originalsourceid><addsrcrecordid>eNpdkc1LxDAQxYMoKqs3zxLw4sHVpOmnF1nrJwiKqNcwSacaaRNNWsH_3qyrop5mYH485r1HyBZn-0WRVQd69DiG_TzPqnSJrCc8L6clL9PlX_sa2QzhmTHGWZGwgq2SNVElWVKIfJ2oGa0hIHUtPTYdDOiho7Wzj2jNENebgGPjwA9P3gUT5lzdwZvRHR7SmaX3Vru-d5Y-gDdghzkA9BY80hMTnG_Qb5CVFrqAm19zQu7PTu_qi-nV9fllPbuaasHYMFUKOZQCEXPIs5aBapUusgyUSpCnFWKjm7Zqmgx0mWpRpZhXQpU6KdOCYSYm5Gih-zKqPsJoh2hGvnjTg3-XDoz8e7HmST66N8m5KEUa85iQ3S8F715HDIPsTdDYdWDRjUEKzpI0ZphUEd35hz670dvoL1KfghGK1N6C0jG94LH9-YYzOS9QLgqUnwVGfPu3gx_4uy7xASCPmR8</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>3111383293</pqid></control><display><type>article</type><title>A Case of Bilateral Congenital Pseudoarthrosis of Clavicle: An Uncommon Variant of a Rare Disorder</title><source>PubMed Central</source><source>PubMed Central Open Access</source><creator>Boeisa, Ahmad N ; Alshammary, Alya A ; Albunyan, Sara ; AlMudayris, Lina ; AlSaeed, Mohammed</creator><creatorcontrib>Boeisa, Ahmad N ; Alshammary, Alya A ; Albunyan, Sara ; AlMudayris, Lina ; AlSaeed, Mohammed</creatorcontrib><description>Congenital pseudarthrosis of the clavicle (CPC) is a rare disorder diagnosed at birth or early childhood presenting with a painless, non-tender mass on the clavicle. Its etiology is unknown, caused by failure of fusion of the medial and lateral ossification centers of the clavicle. Left-sided CPC is rare and linked to other pathological abnormalities. Bilateral involvement is extremely rare and it is seen in association with other congenital malformations. A full-term newborn baby girl was examined after a complicated emergency cesarean section delivery. Upon initial pediatric examination, there was suspicion of bilateral clavicle fracture with no limitation of movement and equal moro reflex bilateral. Plain radiographs of the clavicle revealed a suspected bilateral fracture of the clavicle. At the two-month follow-up, X-rays were taken to assess the clavicle fractures showing persistent bilateral clavicle deformities and there was no interval callus formation which confirmed the diagnosis of bilateral CPC and excluded the presence of the fracture. Bilateral pseudarthrosis of the clavicle is a rare entity, and surgical correction is not required unless the patient develops symptoms of limitations of movement or for aesthetic causes.</description><identifier>ISSN: 2168-8184</identifier><identifier>EISSN: 2168-8184</identifier><identifier>DOI: 10.7759/cureus.66594</identifier><identifier>PMID: 39252736</identifier><language>eng</language><publisher>United States: Cureus Inc</publisher><subject>Asymptomatic ; Case reports ; Congenital diseases ; Cyanosis ; Decision making ; Fractures ; Heart rate ; Intervention ; Intubation ; Management decisions ; Obstetrics/Gynecology ; Orthopedics ; Pain ; Pediatrics ; X-rays</subject><ispartof>Curēus (Palo Alto, CA), 2024-08, Vol.16 (8), p.e66594</ispartof><rights>Copyright © 2024, Boeisa et al.</rights><rights>Copyright © 2024, Boeisa et al. This work is published under https://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>Copyright © 2024, Boeisa et al. 2024 Boeisa et al.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c300t-bbe1a83eee6a65f0abfbc755abb2e149eedcdf9dd5ac84c394e693b8c28470e53</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/PMC11383427/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC11383427/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39252736$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Boeisa, Ahmad N</creatorcontrib><creatorcontrib>Alshammary, Alya A</creatorcontrib><creatorcontrib>Albunyan, Sara</creatorcontrib><creatorcontrib>AlMudayris, Lina</creatorcontrib><creatorcontrib>AlSaeed, Mohammed</creatorcontrib><title>A Case of Bilateral Congenital Pseudoarthrosis of Clavicle: An Uncommon Variant of a Rare Disorder</title><title>Curēus (Palo Alto, CA)</title><addtitle>Cureus</addtitle><description>Congenital pseudarthrosis of the clavicle (CPC) is a rare disorder diagnosed at birth or early childhood presenting with a painless, non-tender mass on the clavicle. Its etiology is unknown, caused by failure of fusion of the medial and lateral ossification centers of the clavicle. Left-sided CPC is rare and linked to other pathological abnormalities. Bilateral involvement is extremely rare and it is seen in association with other congenital malformations. A full-term newborn baby girl was examined after a complicated emergency cesarean section delivery. Upon initial pediatric examination, there was suspicion of bilateral clavicle fracture with no limitation of movement and equal moro reflex bilateral. Plain radiographs of the clavicle revealed a suspected bilateral fracture of the clavicle. At the two-month follow-up, X-rays were taken to assess the clavicle fractures showing persistent bilateral clavicle deformities and there was no interval callus formation which confirmed the diagnosis of bilateral CPC and excluded the presence of the fracture. Bilateral pseudarthrosis of the clavicle is a rare entity, and surgical correction is not required unless the patient develops symptoms of limitations of movement or for aesthetic causes.</description><subject>Asymptomatic</subject><subject>Case reports</subject><subject>Congenital diseases</subject><subject>Cyanosis</subject><subject>Decision making</subject><subject>Fractures</subject><subject>Heart rate</subject><subject>Intervention</subject><subject>Intubation</subject><subject>Management decisions</subject><subject>Obstetrics/Gynecology</subject><subject>Orthopedics</subject><subject>Pain</subject><subject>Pediatrics</subject><subject>X-rays</subject><issn>2168-8184</issn><issn>2168-8184</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>BENPR</sourceid><recordid>eNpdkc1LxDAQxYMoKqs3zxLw4sHVpOmnF1nrJwiKqNcwSacaaRNNWsH_3qyrop5mYH485r1HyBZn-0WRVQd69DiG_TzPqnSJrCc8L6clL9PlX_sa2QzhmTHGWZGwgq2SNVElWVKIfJ2oGa0hIHUtPTYdDOiho7Wzj2jNENebgGPjwA9P3gUT5lzdwZvRHR7SmaX3Vru-d5Y-gDdghzkA9BY80hMTnG_Qb5CVFrqAm19zQu7PTu_qi-nV9fllPbuaasHYMFUKOZQCEXPIs5aBapUusgyUSpCnFWKjm7Zqmgx0mWpRpZhXQpU6KdOCYSYm5Gih-zKqPsJoh2hGvnjTg3-XDoz8e7HmST66N8m5KEUa85iQ3S8F715HDIPsTdDYdWDRjUEKzpI0ZphUEd35hz670dvoL1KfghGK1N6C0jG94LH9-YYzOS9QLgqUnwVGfPu3gx_4uy7xASCPmR8</recordid><startdate>20240810</startdate><enddate>20240810</enddate><creator>Boeisa, Ahmad N</creator><creator>Alshammary, Alya A</creator><creator>Albunyan, Sara</creator><creator>AlMudayris, Lina</creator><creator>AlSaeed, Mohammed</creator><general>Cureus Inc</general><general>Cureus</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20240810</creationdate><title>A Case of Bilateral Congenital Pseudoarthrosis of Clavicle: An Uncommon Variant of a Rare Disorder</title><author>Boeisa, Ahmad N ; Alshammary, Alya A ; Albunyan, Sara ; AlMudayris, Lina ; AlSaeed, Mohammed</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c300t-bbe1a83eee6a65f0abfbc755abb2e149eedcdf9dd5ac84c394e693b8c28470e53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Asymptomatic</topic><topic>Case reports</topic><topic>Congenital diseases</topic><topic>Cyanosis</topic><topic>Decision making</topic><topic>Fractures</topic><topic>Heart rate</topic><topic>Intervention</topic><topic>Intubation</topic><topic>Management decisions</topic><topic>Obstetrics/Gynecology</topic><topic>Orthopedics</topic><topic>Pain</topic><topic>Pediatrics</topic><topic>X-rays</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Boeisa, Ahmad N</creatorcontrib><creatorcontrib>Alshammary, Alya A</creatorcontrib><creatorcontrib>Albunyan, Sara</creatorcontrib><creatorcontrib>AlMudayris, Lina</creatorcontrib><creatorcontrib>AlSaeed, Mohammed</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Curēus (Palo Alto, CA)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Boeisa, Ahmad N</au><au>Alshammary, Alya A</au><au>Albunyan, Sara</au><au>AlMudayris, Lina</au><au>AlSaeed, Mohammed</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A Case of Bilateral Congenital Pseudoarthrosis of Clavicle: An Uncommon Variant of a Rare Disorder</atitle><jtitle>Curēus (Palo Alto, CA)</jtitle><addtitle>Cureus</addtitle><date>2024-08-10</date><risdate>2024</risdate><volume>16</volume><issue>8</issue><spage>e66594</spage><pages>e66594-</pages><issn>2168-8184</issn><eissn>2168-8184</eissn><abstract>Congenital pseudarthrosis of the clavicle (CPC) is a rare disorder diagnosed at birth or early childhood presenting with a painless, non-tender mass on the clavicle. Its etiology is unknown, caused by failure of fusion of the medial and lateral ossification centers of the clavicle. Left-sided CPC is rare and linked to other pathological abnormalities. Bilateral involvement is extremely rare and it is seen in association with other congenital malformations. A full-term newborn baby girl was examined after a complicated emergency cesarean section delivery. Upon initial pediatric examination, there was suspicion of bilateral clavicle fracture with no limitation of movement and equal moro reflex bilateral. Plain radiographs of the clavicle revealed a suspected bilateral fracture of the clavicle. At the two-month follow-up, X-rays were taken to assess the clavicle fractures showing persistent bilateral clavicle deformities and there was no interval callus formation which confirmed the diagnosis of bilateral CPC and excluded the presence of the fracture. Bilateral pseudarthrosis of the clavicle is a rare entity, and surgical correction is not required unless the patient develops symptoms of limitations of movement or for aesthetic causes.</abstract><cop>United States</cop><pub>Cureus Inc</pub><pmid>39252736</pmid><doi>10.7759/cureus.66594</doi><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 2168-8184 |
ispartof | Curēus (Palo Alto, CA), 2024-08, Vol.16 (8), p.e66594 |
issn | 2168-8184 2168-8184 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_11383427 |
source | PubMed Central; PubMed Central Open Access |
subjects | Asymptomatic Case reports Congenital diseases Cyanosis Decision making Fractures Heart rate Intervention Intubation Management decisions Obstetrics/Gynecology Orthopedics Pain Pediatrics X-rays |
title | A Case of Bilateral Congenital Pseudoarthrosis of Clavicle: An Uncommon Variant of a Rare Disorder |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-29T20%3A52%3A12IST&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=A%20Case%20of%20Bilateral%20Congenital%20Pseudoarthrosis%20of%20Clavicle:%20An%20Uncommon%20Variant%20of%20a%20Rare%20Disorder&rft.jtitle=Cur%C4%93us%20(Palo%20Alto,%20CA)&rft.au=Boeisa,%20Ahmad%20N&rft.date=2024-08-10&rft.volume=16&rft.issue=8&rft.spage=e66594&rft.pages=e66594-&rft.issn=2168-8184&rft.eissn=2168-8184&rft_id=info:doi/10.7759/cureus.66594&rft_dat=%3Cproquest_pubme%3E3102472029%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=3111383293&rft_id=info:pmid/39252736&rfr_iscdi=true |