Trigonocephaly - Our Experience and Treatment in the Republic of Macedonia

Prematurely fused metopic suture results in developmental anomaly named trigonocephaly. The treatment of trigonocephaly is a surgical reconstruction, starting from the simple suturectomy toward the complicated cranial vault reconstructions with aim to obtain enough endocranial space for normal devel...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:PRILOZI 2017-03, Vol.38 (1), p.35-40
Hauptverfasser: Mircevsk, Vladimir, Zogovska, Elizabeta, Chaparoski, Aleksandar, Micunovic, Mile, Filipce, Venko, Mirchevski, Mirko Mishel, Kostov, Milenko, Мicunovic, Ljubica
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 40
container_issue 1
container_start_page 35
container_title PRILOZI
container_volume 38
creator Mircevsk, Vladimir
Zogovska, Elizabeta
Chaparoski, Aleksandar
Micunovic, Mile
Filipce, Venko
Mirchevski, Mirko Mishel
Kostov, Milenko
Мicunovic, Ljubica
description Prematurely fused metopic suture results in developmental anomaly named trigonocephaly. The treatment of trigonocephaly is a surgical reconstruction, starting from the simple suturectomy toward the complicated cranial vault reconstructions with aim to obtain enough endocranial space for normal development of the brain and aesthetic correction as well. The aim of our paper is to present our experience on this pathology in the Republic of Macedonia, stressing the trigonocephaly as one of the rare forms of craniosynostosis. Our material: During a period of 20 years (from 1996 to 2015) at the Pediatric department of the Clinic for Neurosurgery in Skopje, we observed 18 babies with trigonocephaly, including one with Carpenter syndrome and trigonocephaly, 14 males and 4 females. All children had simple trigonocephaly, one had syndromic trigonocephaly (Carpenter's syndrome). According to Oi and Matsumoto classification done in 19865 severe trigonocephaly is observed in 11 cases and, moderate trigonocephaly in 7 cases. Our method: Our treatment consisted of slightly modified Di Rocco's3 surgical procedure named "shell" operation, adding transposition of the "bone flap". The postoperative period was uneventful except for the expected forehead swelling. The babies were discharged from the hospital on average at the 8th postoperative day. At the three months control after the surgery, the head had excellent aesthetic appearance, with regular psychomotor development according to the age of the patient (Fig 3а and 3b). We had no serious complications except the expected postoperative swelling of the forehead. All operated children had excellent "long term" aesthetic effect and normal psychomotor development. The early recognition of these anomalies including all craniosynostoses, the deformities of the newborn and infant's head and the preventive operative reconstruction would prevent abnormal disturbance of the psychomotor development during the child's growth. The multidisciplinary approach can prevent new disabled individuals in the society. Our technique allows shortening the entire surgical procedure, especially in the departments where blood saving devices are not available.
doi_str_mv 10.1515/prilozi-2017-0004
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1907322459</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>3157108921</sourcerecordid><originalsourceid>FETCH-LOGICAL-c2245-6fb543481323001aa0afa208401247eb65a2927d80e78e063d12d2ca1be639a03</originalsourceid><addsrcrecordid>eNpdkE1Lw0AQhhdRrNT-AC-y4MVLdGc3m2yOUuoXlYLU87LZTGxKko2bBKy_3oRWEU8zh-d9Z3gIuQB2AxLkbeOL0n0VAWcQB4yx8IicgZJxkIhQHv_ZJ2TWttuBgAikEvKUTLiSiVCJOCPPa1-8u9pZbDam3NGArnpPF58N-gJri9TUGV17NF2FdUeLmnYbpK_Y9GlZWOpy-mIsZq4uzDk5yU3Z4uwwp-TtfrGePwbL1cPT_G4ZWM5DGUR5KkMRKhBcDD8Zw0xuOFMhAx7GmEbS8ITHmWIYK2SRyIBn3BpIMRKJYWJKrve9jXcfPbadrorWYlmaGl3fakhYLMZTyYBe_UO3rvf18J0WIGNgKuEwULCnrHdt6zHXg9vK-J0GpkfX-uBaj6716HrIXB6a-7TC7DfxY1Z8A_SZeQM</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>3157108921</pqid></control><display><type>article</type><title>Trigonocephaly - Our Experience and Treatment in the Republic of Macedonia</title><source>MEDLINE</source><source>De Gruyter Open Access Journals</source><source>Alma/SFX Local Collection</source><creator>Mircevsk, Vladimir ; Zogovska, Elizabeta ; Chaparoski, Aleksandar ; Micunovic, Mile ; Filipce, Venko ; Mirchevski, Mirko Mishel ; Kostov, Milenko ; Мicunovic, Ljubica</creator><creatorcontrib>Mircevsk, Vladimir ; Zogovska, Elizabeta ; Chaparoski, Aleksandar ; Micunovic, Mile ; Filipce, Venko ; Mirchevski, Mirko Mishel ; Kostov, Milenko ; Мicunovic, Ljubica</creatorcontrib><description>Prematurely fused metopic suture results in developmental anomaly named trigonocephaly. The treatment of trigonocephaly is a surgical reconstruction, starting from the simple suturectomy toward the complicated cranial vault reconstructions with aim to obtain enough endocranial space for normal development of the brain and aesthetic correction as well. The aim of our paper is to present our experience on this pathology in the Republic of Macedonia, stressing the trigonocephaly as one of the rare forms of craniosynostosis. Our material: During a period of 20 years (from 1996 to 2015) at the Pediatric department of the Clinic for Neurosurgery in Skopje, we observed 18 babies with trigonocephaly, including one with Carpenter syndrome and trigonocephaly, 14 males and 4 females. All children had simple trigonocephaly, one had syndromic trigonocephaly (Carpenter's syndrome). According to Oi and Matsumoto classification done in 19865 severe trigonocephaly is observed in 11 cases and, moderate trigonocephaly in 7 cases. Our method: Our treatment consisted of slightly modified Di Rocco's3 surgical procedure named "shell" operation, adding transposition of the "bone flap". The postoperative period was uneventful except for the expected forehead swelling. The babies were discharged from the hospital on average at the 8th postoperative day. At the three months control after the surgery, the head had excellent aesthetic appearance, with regular psychomotor development according to the age of the patient (Fig 3а and 3b). We had no serious complications except the expected postoperative swelling of the forehead. All operated children had excellent "long term" aesthetic effect and normal psychomotor development. The early recognition of these anomalies including all craniosynostoses, the deformities of the newborn and infant's head and the preventive operative reconstruction would prevent abnormal disturbance of the psychomotor development during the child's growth. The multidisciplinary approach can prevent new disabled individuals in the society. Our technique allows shortening the entire surgical procedure, especially in the departments where blood saving devices are not available.</description><identifier>ISSN: 1857-9345</identifier><identifier>ISSN: 1857-8985</identifier><identifier>EISSN: 1857-9345</identifier><identifier>EISSN: 1857-8985</identifier><identifier>EISSN: 0350-1914</identifier><identifier>DOI: 10.1515/prilozi-2017-0004</identifier><identifier>PMID: 28593893</identifier><language>eng</language><publisher>Macedonia: De Gruyter Poland</publisher><subject>Acrocephalosyndactylia - diagnostic imaging ; Acrocephalosyndactylia - epidemiology ; Acrocephalosyndactylia - surgery ; Age Factors ; Child Development ; Cranial Sutures - abnormalities ; Cranial Sutures - diagnostic imaging ; Cranial Sutures - surgery ; Craniosynostoses - diagnostic imaging ; Craniosynostoses - epidemiology ; Craniosynostoses - surgery ; Female ; Humans ; Infant ; Infant, Newborn ; Macedonia (Republic) - epidemiology ; Male ; Neurosurgical Procedures - adverse effects ; Neurosurgical Procedures - methods ; Postoperative Complications - etiology ; Reconstructive Surgical Procedures - adverse effects ; Reconstructive Surgical Procedures - methods ; Time Factors ; Tomography, X-Ray Computed ; Treatment Outcome</subject><ispartof>PRILOZI, 2017-03, Vol.38 (1), p.35-40</ispartof><rights>2017. This work is published under http://creativecommons.org/licenses/by-nc-nd/4.0 (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c2245-6fb543481323001aa0afa208401247eb65a2927d80e78e063d12d2ca1be639a03</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/28593893$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mircevsk, Vladimir</creatorcontrib><creatorcontrib>Zogovska, Elizabeta</creatorcontrib><creatorcontrib>Chaparoski, Aleksandar</creatorcontrib><creatorcontrib>Micunovic, Mile</creatorcontrib><creatorcontrib>Filipce, Venko</creatorcontrib><creatorcontrib>Mirchevski, Mirko Mishel</creatorcontrib><creatorcontrib>Kostov, Milenko</creatorcontrib><creatorcontrib>Мicunovic, Ljubica</creatorcontrib><title>Trigonocephaly - Our Experience and Treatment in the Republic of Macedonia</title><title>PRILOZI</title><addtitle>Pril (Makedon Akad Nauk Umet Odd Med Nauki)</addtitle><description>Prematurely fused metopic suture results in developmental anomaly named trigonocephaly. The treatment of trigonocephaly is a surgical reconstruction, starting from the simple suturectomy toward the complicated cranial vault reconstructions with aim to obtain enough endocranial space for normal development of the brain and aesthetic correction as well. The aim of our paper is to present our experience on this pathology in the Republic of Macedonia, stressing the trigonocephaly as one of the rare forms of craniosynostosis. Our material: During a period of 20 years (from 1996 to 2015) at the Pediatric department of the Clinic for Neurosurgery in Skopje, we observed 18 babies with trigonocephaly, including one with Carpenter syndrome and trigonocephaly, 14 males and 4 females. All children had simple trigonocephaly, one had syndromic trigonocephaly (Carpenter's syndrome). According to Oi and Matsumoto classification done in 19865 severe trigonocephaly is observed in 11 cases and, moderate trigonocephaly in 7 cases. Our method: Our treatment consisted of slightly modified Di Rocco's3 surgical procedure named "shell" operation, adding transposition of the "bone flap". The postoperative period was uneventful except for the expected forehead swelling. The babies were discharged from the hospital on average at the 8th postoperative day. At the three months control after the surgery, the head had excellent aesthetic appearance, with regular psychomotor development according to the age of the patient (Fig 3а and 3b). We had no serious complications except the expected postoperative swelling of the forehead. All operated children had excellent "long term" aesthetic effect and normal psychomotor development. The early recognition of these anomalies including all craniosynostoses, the deformities of the newborn and infant's head and the preventive operative reconstruction would prevent abnormal disturbance of the psychomotor development during the child's growth. The multidisciplinary approach can prevent new disabled individuals in the society. Our technique allows shortening the entire surgical procedure, especially in the departments where blood saving devices are not available.</description><subject>Acrocephalosyndactylia - diagnostic imaging</subject><subject>Acrocephalosyndactylia - epidemiology</subject><subject>Acrocephalosyndactylia - surgery</subject><subject>Age Factors</subject><subject>Child Development</subject><subject>Cranial Sutures - abnormalities</subject><subject>Cranial Sutures - diagnostic imaging</subject><subject>Cranial Sutures - surgery</subject><subject>Craniosynostoses - diagnostic imaging</subject><subject>Craniosynostoses - epidemiology</subject><subject>Craniosynostoses - surgery</subject><subject>Female</subject><subject>Humans</subject><subject>Infant</subject><subject>Infant, Newborn</subject><subject>Macedonia (Republic) - epidemiology</subject><subject>Male</subject><subject>Neurosurgical Procedures - adverse effects</subject><subject>Neurosurgical Procedures - methods</subject><subject>Postoperative Complications - etiology</subject><subject>Reconstructive Surgical Procedures - adverse effects</subject><subject>Reconstructive Surgical Procedures - methods</subject><subject>Time Factors</subject><subject>Tomography, X-Ray Computed</subject><subject>Treatment Outcome</subject><issn>1857-9345</issn><issn>1857-8985</issn><issn>1857-9345</issn><issn>1857-8985</issn><issn>0350-1914</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNpdkE1Lw0AQhhdRrNT-AC-y4MVLdGc3m2yOUuoXlYLU87LZTGxKko2bBKy_3oRWEU8zh-d9Z3gIuQB2AxLkbeOL0n0VAWcQB4yx8IicgZJxkIhQHv_ZJ2TWttuBgAikEvKUTLiSiVCJOCPPa1-8u9pZbDam3NGArnpPF58N-gJri9TUGV17NF2FdUeLmnYbpK_Y9GlZWOpy-mIsZq4uzDk5yU3Z4uwwp-TtfrGePwbL1cPT_G4ZWM5DGUR5KkMRKhBcDD8Zw0xuOFMhAx7GmEbS8ITHmWIYK2SRyIBn3BpIMRKJYWJKrve9jXcfPbadrorWYlmaGl3fakhYLMZTyYBe_UO3rvf18J0WIGNgKuEwULCnrHdt6zHXg9vK-J0GpkfX-uBaj6716HrIXB6a-7TC7DfxY1Z8A_SZeQM</recordid><startdate>20170301</startdate><enddate>20170301</enddate><creator>Mircevsk, Vladimir</creator><creator>Zogovska, Elizabeta</creator><creator>Chaparoski, Aleksandar</creator><creator>Micunovic, Mile</creator><creator>Filipce, Venko</creator><creator>Mirchevski, Mirko Mishel</creator><creator>Kostov, Milenko</creator><creator>Мicunovic, Ljubica</creator><general>De Gruyter Poland</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>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>20170301</creationdate><title>Trigonocephaly - Our Experience and Treatment in the Republic of Macedonia</title><author>Mircevsk, Vladimir ; Zogovska, Elizabeta ; Chaparoski, Aleksandar ; Micunovic, Mile ; Filipce, Venko ; Mirchevski, Mirko Mishel ; Kostov, Milenko ; Мicunovic, Ljubica</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2245-6fb543481323001aa0afa208401247eb65a2927d80e78e063d12d2ca1be639a03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Acrocephalosyndactylia - diagnostic imaging</topic><topic>Acrocephalosyndactylia - epidemiology</topic><topic>Acrocephalosyndactylia - surgery</topic><topic>Age Factors</topic><topic>Child Development</topic><topic>Cranial Sutures - abnormalities</topic><topic>Cranial Sutures - diagnostic imaging</topic><topic>Cranial Sutures - surgery</topic><topic>Craniosynostoses - diagnostic imaging</topic><topic>Craniosynostoses - epidemiology</topic><topic>Craniosynostoses - surgery</topic><topic>Female</topic><topic>Humans</topic><topic>Infant</topic><topic>Infant, Newborn</topic><topic>Macedonia (Republic) - epidemiology</topic><topic>Male</topic><topic>Neurosurgical Procedures - adverse effects</topic><topic>Neurosurgical Procedures - methods</topic><topic>Postoperative Complications - etiology</topic><topic>Reconstructive Surgical Procedures - adverse effects</topic><topic>Reconstructive Surgical Procedures - methods</topic><topic>Time Factors</topic><topic>Tomography, X-Ray Computed</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mircevsk, Vladimir</creatorcontrib><creatorcontrib>Zogovska, Elizabeta</creatorcontrib><creatorcontrib>Chaparoski, Aleksandar</creatorcontrib><creatorcontrib>Micunovic, Mile</creatorcontrib><creatorcontrib>Filipce, Venko</creatorcontrib><creatorcontrib>Mirchevski, Mirko Mishel</creatorcontrib><creatorcontrib>Kostov, Milenko</creatorcontrib><creatorcontrib>Мicunovic, Ljubica</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</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>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><jtitle>PRILOZI</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mircevsk, Vladimir</au><au>Zogovska, Elizabeta</au><au>Chaparoski, Aleksandar</au><au>Micunovic, Mile</au><au>Filipce, Venko</au><au>Mirchevski, Mirko Mishel</au><au>Kostov, Milenko</au><au>Мicunovic, Ljubica</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Trigonocephaly - Our Experience and Treatment in the Republic of Macedonia</atitle><jtitle>PRILOZI</jtitle><addtitle>Pril (Makedon Akad Nauk Umet Odd Med Nauki)</addtitle><date>2017-03-01</date><risdate>2017</risdate><volume>38</volume><issue>1</issue><spage>35</spage><epage>40</epage><pages>35-40</pages><issn>1857-9345</issn><issn>1857-8985</issn><eissn>1857-9345</eissn><eissn>1857-8985</eissn><eissn>0350-1914</eissn><abstract>Prematurely fused metopic suture results in developmental anomaly named trigonocephaly. The treatment of trigonocephaly is a surgical reconstruction, starting from the simple suturectomy toward the complicated cranial vault reconstructions with aim to obtain enough endocranial space for normal development of the brain and aesthetic correction as well. The aim of our paper is to present our experience on this pathology in the Republic of Macedonia, stressing the trigonocephaly as one of the rare forms of craniosynostosis. Our material: During a period of 20 years (from 1996 to 2015) at the Pediatric department of the Clinic for Neurosurgery in Skopje, we observed 18 babies with trigonocephaly, including one with Carpenter syndrome and trigonocephaly, 14 males and 4 females. All children had simple trigonocephaly, one had syndromic trigonocephaly (Carpenter's syndrome). According to Oi and Matsumoto classification done in 19865 severe trigonocephaly is observed in 11 cases and, moderate trigonocephaly in 7 cases. Our method: Our treatment consisted of slightly modified Di Rocco's3 surgical procedure named "shell" operation, adding transposition of the "bone flap". The postoperative period was uneventful except for the expected forehead swelling. The babies were discharged from the hospital on average at the 8th postoperative day. At the three months control after the surgery, the head had excellent aesthetic appearance, with regular psychomotor development according to the age of the patient (Fig 3а and 3b). We had no serious complications except the expected postoperative swelling of the forehead. All operated children had excellent "long term" aesthetic effect and normal psychomotor development. The early recognition of these anomalies including all craniosynostoses, the deformities of the newborn and infant's head and the preventive operative reconstruction would prevent abnormal disturbance of the psychomotor development during the child's growth. The multidisciplinary approach can prevent new disabled individuals in the society. Our technique allows shortening the entire surgical procedure, especially in the departments where blood saving devices are not available.</abstract><cop>Macedonia</cop><pub>De Gruyter Poland</pub><pmid>28593893</pmid><doi>10.1515/prilozi-2017-0004</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1857-9345
ispartof PRILOZI, 2017-03, Vol.38 (1), p.35-40
issn 1857-9345
1857-8985
1857-9345
1857-8985
0350-1914
language eng
recordid cdi_proquest_miscellaneous_1907322459
source MEDLINE; De Gruyter Open Access Journals; Alma/SFX Local Collection
subjects Acrocephalosyndactylia - diagnostic imaging
Acrocephalosyndactylia - epidemiology
Acrocephalosyndactylia - surgery
Age Factors
Child Development
Cranial Sutures - abnormalities
Cranial Sutures - diagnostic imaging
Cranial Sutures - surgery
Craniosynostoses - diagnostic imaging
Craniosynostoses - epidemiology
Craniosynostoses - surgery
Female
Humans
Infant
Infant, Newborn
Macedonia (Republic) - epidemiology
Male
Neurosurgical Procedures - adverse effects
Neurosurgical Procedures - methods
Postoperative Complications - etiology
Reconstructive Surgical Procedures - adverse effects
Reconstructive Surgical Procedures - methods
Time Factors
Tomography, X-Ray Computed
Treatment Outcome
title Trigonocephaly - Our Experience and Treatment in the Republic of Macedonia
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-05T09%3A46%3A25IST&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=Trigonocephaly%20-%20Our%20Experience%20and%20Treatment%20in%20the%20Republic%20of%20Macedonia&rft.jtitle=PRILOZI&rft.au=Mircevsk,%20Vladimir&rft.date=2017-03-01&rft.volume=38&rft.issue=1&rft.spage=35&rft.epage=40&rft.pages=35-40&rft.issn=1857-9345&rft.eissn=1857-9345&rft_id=info:doi/10.1515/prilozi-2017-0004&rft_dat=%3Cproquest_cross%3E3157108921%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=3157108921&rft_id=info:pmid/28593893&rfr_iscdi=true