Large aplasia cutis congenita of the vertex conservative management
Background Aplasia cutis congenita (ACC) of the vertex with bone defect is a rare and begnin anomaly that can involve the epidermis, dermis, and subcutaneous tissues of the scalp with significant bone defect Bajpai and Pal (J Pediatr Surg 38(2):e4, 2003). When associated with skull defect, this rare...
Saved in:
Published in: | Child's nervous system Vol. 40; no. 2; pp. 285 - 292 |
---|---|
Main Authors: | , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
Berlin/Heidelberg
Springer Berlin Heidelberg
01-02-2024
|
Subjects: | |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Abstract | Background
Aplasia cutis congenita (ACC) of the vertex with bone defect is a rare and begnin anomaly that can involve the epidermis, dermis, and subcutaneous tissues of the scalp with significant bone defect Bajpai and Pal (J Pediatr Surg 38(2):e4, 2003). When associated with skull defect, this rare malformation carries the risk of severe complications such as rupture of the superior sagittal sinus or infections.
Methods and results
We report a case of aplasia cutis congenita of the scalp with skull defect measuring 9 × 10 cm and an exposed sagittal sinus in a newborn. Both conservative and surgical methods have been proposed to treat this condition. In our case, conservative treatment was planned led to complete epithelization and the patient was healing well at 5 years of follow-up.
Conclusions
ACC of the vertex with a large scalp defects present a management dilemma Rocha et al. (Clin Case Rep 3(10):841–4, 2015). Based on a review of the literature, we report this case to demonstrate that even for the largest skin and bone defects, an initial conservative approach may allow for complete wound closure without the need for early surgical intervention. |
---|---|
AbstractList | Background
Aplasia cutis congenita (ACC) of the vertex with bone defect is a rare and begnin anomaly that can involve the epidermis, dermis, and subcutaneous tissues of the scalp with significant bone defect Bajpai and Pal (J Pediatr Surg 38(2):e4, 2003). When associated with skull defect, this rare malformation carries the risk of severe complications such as rupture of the superior sagittal sinus or infections.
Methods and results
We report a case of aplasia cutis congenita of the scalp with skull defect measuring 9 × 10 cm and an exposed sagittal sinus in a newborn. Both conservative and surgical methods have been proposed to treat this condition. In our case, conservative treatment was planned led to complete epithelization and the patient was healing well at 5 years of follow-up.
Conclusions
ACC of the vertex with a large scalp defects present a management dilemma Rocha et al. (Clin Case Rep 3(10):841–4, 2015). Based on a review of the literature, we report this case to demonstrate that even for the largest skin and bone defects, an initial conservative approach may allow for complete wound closure without the need for early surgical intervention. BACKGROUNDAplasia cutis congenita (ACC) of the vertex with bone defect is a rare and begnin anomaly that can involve the epidermis, dermis, and subcutaneous tissues of the scalp with significant bone defect Bajpai and Pal (J Pediatr Surg 38(2):e4, 2003). When associated with skull defect, this rare malformation carries the risk of severe complications such as rupture of the superior sagittal sinus or infections.METHODS AND RESULTSWe report a case of aplasia cutis congenita of the scalp with skull defect measuring 9 × 10 cm and an exposed sagittal sinus in a newborn. Both conservative and surgical methods have been proposed to treat this condition. In our case, conservative treatment was planned led to complete epithelization and the patient was healing well at 5 years of follow-up.CONCLUSIONSACC of the vertex with a large scalp defects present a management dilemma Rocha et al. (Clin Case Rep 3(10):841-4, 2015). Based on a review of the literature, we report this case to demonstrate that even for the largest skin and bone defects, an initial conservative approach may allow for complete wound closure without the need for early surgical intervention. Aplasia cutis congenita (ACC) of the vertex with bone defect is a rare and begnin anomaly that can involve the epidermis, dermis, and subcutaneous tissues of the scalp with significant bone defect Bajpai and Pal (J Pediatr Surg 38(2):e4, 2003). When associated with skull defect, this rare malformation carries the risk of severe complications such as rupture of the superior sagittal sinus or infections. We report a case of aplasia cutis congenita of the scalp with skull defect measuring 9 × 10 cm and an exposed sagittal sinus in a newborn. Both conservative and surgical methods have been proposed to treat this condition. In our case, conservative treatment was planned led to complete epithelization and the patient was healing well at 5 years of follow-up. ACC of the vertex with a large scalp defects present a management dilemma Rocha et al. (Clin Case Rep 3(10):841-4, 2015). Based on a review of the literature, we report this case to demonstrate that even for the largest skin and bone defects, an initial conservative approach may allow for complete wound closure without the need for early surgical intervention. |
Author | Mechergui, Haifa Charfeddine, Sarah Houimli Abderrahmen, Khansa Bouali, Sofiene Kallel, Jalel Ghedira, Khalil |
Author_xml | – sequence: 1 givenname: Sofiene surname: Bouali fullname: Bouali, Sofiene email: sofienebouali@hotmail.fr organization: Department of Neurosurgery, National Institute of Neurology”Mongi Ben Hmida”, Tunis Faculty of Medicine, University of Tunis El Manar – sequence: 2 givenname: Sarah Houimli surname: Charfeddine fullname: Charfeddine, Sarah Houimli organization: Reconstructive & Aesthetic Surgery Department – sequence: 3 givenname: Khalil surname: Ghedira fullname: Ghedira, Khalil organization: Department of Neurosurgery, National Institute of Neurology”Mongi Ben Hmida”, Tunis Faculty of Medicine, University of Tunis El Manar – sequence: 4 givenname: Haifa surname: Mechergui fullname: Mechergui, Haifa organization: Department of Neurosurgery, National Institute of Neurology”Mongi Ben Hmida”, Tunis Faculty of Medicine, University of Tunis El Manar – sequence: 5 givenname: Khansa surname: Abderrahmen fullname: Abderrahmen, Khansa organization: Department of Neurosurgery, National Institute of Neurology”Mongi Ben Hmida”, Tunis Faculty of Medicine, University of Tunis El Manar – sequence: 6 givenname: Jalel surname: Kallel fullname: Kallel, Jalel organization: Department of Neurosurgery, National Institute of Neurology”Mongi Ben Hmida”, Tunis Faculty of Medicine, University of Tunis El Manar |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/37865964$$D View this record in MEDLINE/PubMed |
BookMark | eNp9kE9PwzAMxSM0xMbgC3BAPXIpOEmTtEc08U-axAXOkdu6o9PajqSdxrcno4MjJ8v2e0_275xN2q4lxq443HIAc-cBZMpjEDIGzTOI9ydsxhMZWqlgwmYglI4NJDBl596vAbhKRXbGptKkWmU6mbHFEt2KItxu0NcYFUNf-6jo2hW1dY9RV0X9B0U7cj3tD3NPbod9vaOowRZX1FDbX7DTCjeeLo91zt4fH94Wz_Hy9ellcb-MC5mYPhbIpcoyDaI0UlMljcISsFBCoS7D2ZokktSojOZ5ZfJMiYpMBqnMSeQg5-xmzN267nMg39um9gVtNthSN3gr0hRSwRUcpGKUFq7z3lFlt65u0H1ZDvYAz47wbIBnf-DZfTBdH_OHvKHyz_JLKwjkKPBhFRA5u-4G14af_4v9BvNXfBc |
CitedBy_id | crossref_primary_10_7759_cureus_63215 |
Cites_doi | 10.30699/jogcr.5.4.172 10.1016/j.anpede.2015.09.010 10.1111/j.1346-8138.2002.tb00285.x 10.1111/ijd.13008 10.1053/jpsu.2003.50064 10.1097/00001665-200207000-00003 10.1054/bjps.2000.3406 10.1001/archderm.1974.01630100071018 10.1111/j.1525-1470.2010.01266.x 10.1097/SCS.0000000000003347 10.1007/s12024-014-9645-5 10.1054/bjps.2002.3963 10.1002/ccr3.4671 10.1016/S0190-9622(86)70082-0 10.1038/jp.2008.250 10.1097/00001665-200207000-00007 10.1055/s-2003-39562 10.1016/S0002-9378(16)41979-4 10.1371/journal.pgen.1003573 10.1097/SCS.0000000000001798 10.4103/sni.sni_188_17 10.1097/01.scs.0000246500.84935.4f 10.1055/s-0034-1387195 10.46900/apn.v4i1(January-April).109 10.1159/000442989 10.1001/archderm.141.5.554 10.1097/SCS.0000000000002610 10.1007/s00381-002-0654-4 10.1155/2016/4264721 10.1002/ccr3.361 |
ContentType | Journal Article |
Copyright | The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. 2023. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature. |
Copyright_xml | – notice: The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. – notice: 2023. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature. |
DBID | NPM AAYXX CITATION 7X8 |
DOI | 10.1007/s00381-023-06190-x |
DatabaseName | PubMed CrossRef MEDLINE - Academic |
DatabaseTitle | PubMed CrossRef MEDLINE - Academic |
DatabaseTitleList | MEDLINE - Academic PubMed |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Medicine |
EISSN | 1433-0350 |
EndPage | 292 |
ExternalDocumentID | 10_1007_s00381_023_06190_x 37865964 |
Genre | Journal Article Review |
GroupedDBID | --- -53 -5E -5G -BR -EM -Y2 -~C .86 .GJ .VR 06C 06D 0R~ 0VY 1N0 1SB 2.D 203 29B 29~ 2J2 2JN 2JY 2KG 2KM 2LR 2P1 2VQ 2~H 30V 4.4 406 408 409 40D 40E 53G 5QI 5RE 5VS 67Z 6NX 78A 8TC 8UJ 95- 95. 95~ 96X AAAVM AABHQ AABYN AAFGU AAHNG AAIAL AAJKR AAKSU AANXM AANZL AARHV AARTL AATNV AATVU AAUYE AAWCG AAYFA AAYIU AAYQN AAYTO ABBBX ABBXA ABDZT ABECU ABFGW ABFTV ABHLI ABHQN ABIPD ABJNI ABJOX ABKAS ABKCH ABKTR ABMNI ABMQK ABNWP ABPLI ABQBU ABSXP ABTEG ABTKH ABTMW ABULA ABUWZ ABWNU ABXPI ACAOD ACBMV ACBRV ACBXY ACBYP ACGFS ACHSB ACHXU ACIGE ACIPQ ACKNC ACMDZ ACMLO ACOKC ACOMO ACTTH ACUDM ACVWB ACWMK ACZOJ ADHHG ADHIR ADIMF ADINQ ADJJI ADKNI ADKPE ADMDM ADOXG ADRFC ADTPH ADURQ ADYFF ADZKW AEBTG AEEQQ AEFIE AEFTE AEGAL AEGNC AEJHL AEJRE AEKMD AENEX AEOHA AEPYU AESKC AESTI AETLH AEVLU AEVTX AEXYK AFAFS AFEXP AFFNX AFLOW AFNRJ AFQWF AFWTZ AFZKB AGAYW AGDGC AGGBP AGGDS AGJBK AGKHE AGMZJ AGQMX AGWIL AGWZB AGYKE AHAVH AHBYD AHIZS AHKAY AHSBF AHYZX AIAKS AIIXL AILAN AIMYW AITGF AJBLW AJDOV AJRNO AJZVZ AKMHD AKQUC ALMA_UNASSIGNED_HOLDINGS ALWAN AMKLP AMXSW AMYLF AMYQR AOCGG ARMRJ ASPBG AVWKF AXYYD AZFZN B-. BA0 BDATZ BGNMA CAG COF CSCUP DDRTE DL5 DNIVK DPUIP DU5 EBD EBLON EBS EIOEI EJD EMB EMOBN EN4 ESBYG F5P FEDTE FERAY FFXSO FIGPU FINBP FNLPD FRRFC FSGXE FWDCC G-Y G-Z GGCAI GGRSB GJIRD GNWQR GQ6 GQ7 GQ8 GRRUI GXS HF~ HG5 HG6 HMJXF HQYDN HRMNR HVGLF HZ~ I09 IHE IJ- IKXTQ IMOTQ IWAJR IXC IXD IXE IZIGR IZQ I~X I~Z J-C J0Z JBSCW JCJTX JZLTJ KDC KOV KOW KPH LAS LLZTM M4Y MA- N2Q N9A NB0 NDZJH NPVJJ NQJWS NU0 O9- O93 O9G O9I O9J OAM OVD P19 P2P P9S PF0 PT4 PT5 QOK QOR QOS R4E R89 R9I RHV RIG RNI ROL RPX RRX RSV RZK S16 S1Z S26 S27 S28 S37 S3B SAP SCLPG SDE SDH SDM SHX SISQX SJYHP SMD SNE SNPRN SNX SOHCF SOJ SPISZ SRMVM SSLCW SSXJD STPWE SV3 SZ9 SZN T13 T16 TEORI TSG TSK TSV TT1 TUC U2A U9L UG4 UNUBA UOJIU UTJUX UZXMN VC2 VFIZW W23 W48 WJK WK8 YLTOR Z45 Z5O Z7U Z81 Z82 Z86 Z87 Z8O Z8U Z8V Z91 ZGI ZMTXR ZOVNA ~EX AACDK AAEOY AAJBT AASML AAYZH ABAKF ACDTI AEFQL AEMSY AFBBN AGQEE AGRTI AIGIU AJOOF H13 NPM AAYXX CITATION 7X8 |
ID | FETCH-LOGICAL-c347t-2a13599602d736ef375ad0ac525a6d4336e3ae36a5761bf7b952fe79083be2b03 |
IEDL.DBID | AEJHL |
ISSN | 0256-7040 |
IngestDate | Fri Oct 25 07:33:44 EDT 2024 Thu Nov 21 21:03:45 EST 2024 Sat Nov 02 12:22:29 EDT 2024 Sat Feb 03 01:18:37 EST 2024 |
IsPeerReviewed | true |
IsScholarly | true |
Issue | 2 |
Keywords | Acutis dermal dysplasia Scalp defects Bone defect Conservative treatment |
Language | English |
License | 2023. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature. |
LinkModel | DirectLink |
MergedId | FETCHMERGED-LOGICAL-c347t-2a13599602d736ef375ad0ac525a6d4336e3ae36a5761bf7b952fe79083be2b03 |
Notes | ObjectType-Case Study-2 SourceType-Scholarly Journals-1 ObjectType-Review-3 content type line 23 ObjectType-Feature-5 ObjectType-Article-4 ObjectType-Report-1 |
PMID | 37865964 |
PQID | 2880821500 |
PQPubID | 23479 |
PageCount | 8 |
ParticipantIDs | proquest_miscellaneous_2880821500 crossref_primary_10_1007_s00381_023_06190_x pubmed_primary_37865964 springer_journals_10_1007_s00381_023_06190_x |
PublicationCentury | 2000 |
PublicationDate | 2024-02-01 |
PublicationDateYYYYMMDD | 2024-02-01 |
PublicationDate_xml | – month: 02 year: 2024 text: 2024-02-01 day: 01 |
PublicationDecade | 2020 |
PublicationPlace | Berlin/Heidelberg |
PublicationPlace_xml | – name: Berlin/Heidelberg – name: Germany |
PublicationTitle | Child's nervous system |
PublicationTitleAbbrev | Childs Nerv Syst |
PublicationTitleAlternate | Childs Nerv Syst |
PublicationYear | 2024 |
Publisher | Springer Berlin Heidelberg |
Publisher_xml | – name: Springer Berlin Heidelberg |
References | Starcevic, SepecMP (CR19) 2010; 27 Rhee, Colville, Buchman, Muraszko (CR22) 2002; 13 Alexondros, Dimitrios, Elias, Evangelis, Andreas, Sotirios (CR14) 2017; 8 CR18 Caksen, Kurtoglu (CR1) 2002; 29 Ingall (CR9) 1933; 25 CR12 CR31 Basterzi, Bagdatoglu, Sari (CR24) 2007; 18 CR30 Kuang, Zhang, Chen, Zhao, Li (CR17) 2014; 26 Yang (CR20) 2000; 53 CR2 CR4 CR5 Marneros (CR7) 2013; 9 Bang, Ghoneim, Gang, Al Najjadah (CR23) 2003; 13 Komuro, Yanai, Seno (CR3) 2002; 13 Frieden (CR11) 1986; 14 Sohrabi, Yousefi-Sharmi, Sohrabi (CR15) 2020; 5 Rudolph, SchwartzW (CR10) 1974; 110 Frojd, Maltese, Kolby (CR26) 2014; 75 Maeda, Oyama, Funayama (CR27) 2015; 26 Orgun, Horiguchi, Hayashi, Shimoji, Arai, Mizuno (CR8) 2017; 28 Puvabanditsin, February, Garrow (CR29) 2016; 55 Saraiya (CR21) 2002; 55 Bajpai, Pal (CR6) 2003; 38 Betancourth-Alvarenga, Vázquez-Rueda, Vargas-Cruz, Paredes-Esteban, Ayala-Montoro (CR28) 2015; 83 Johnson, Offiah, Cohen (CR13) 2015; 11 Wu, Liu, Luo (CR16) 2021; 9 Burkhead, Poindexter, Morrell (CR25) 2009; 29 H Caksen (6190_CR1) 2002; 29 JY Yang (6190_CR20) 2000; 53 R Johnson (6190_CR13) 2015; 11 T Maeda (6190_CR27) 2015; 26 S Puvabanditsin (6190_CR29) 2016; 55 RI Rudolph (6190_CR10) 1974; 110 B Alexondros (6190_CR14) 2017; 8 M Starcevic (6190_CR19) 2010; 27 ST Rhee (6190_CR22) 2002; 13 6190_CR12 6190_CR2 6190_CR31 6190_CR30 JE Betancourth-Alvarenga (6190_CR28) 2015; 83 M Bajpai (6190_CR6) 2003; 38 V Frojd (6190_CR26) 2014; 75 6190_CR5 D Orgun (6190_CR8) 2017; 28 Y Wu (6190_CR16) 2021; 9 6190_CR4 AG Marneros (6190_CR7) 2013; 9 Y Basterzi (6190_CR24) 2007; 18 NW Ingall (6190_CR9) 1933; 25 IJ Frieden (6190_CR11) 1986; 14 A Burkhead (6190_CR25) 2009; 29 Y Komuro (6190_CR3) 2002; 13 F Kuang (6190_CR17) 2014; 26 6190_CR18 HA Saraiya (6190_CR21) 2002; 55 RL Bang (6190_CR23) 2003; 13 H Sohrabi (6190_CR15) 2020; 5 |
References_xml | – volume: 5 start-page: 172 issue: 4 year: 2020 end-page: 174 ident: CR15 article-title: Extensive aplasia cutis congenita a case report publication-title: J Obstet Gynecol Cancer Res doi: 10.30699/jogcr.5.4.172 contributor: fullname: Sohrabi – ident: CR18 – volume: 83 start-page: 341 year: 2015 end-page: 345 ident: CR28 article-title: Manejoquirúrgico de la aplasia cutis congénita publication-title: An Pediatr (Barc) doi: 10.1016/j.anpede.2015.09.010 contributor: fullname: Ayala-Montoro – volume: 29 start-page: 376 issue: 6 year: 2002 end-page: 379 ident: CR1 article-title: Our experience with aplasia cutis congenita publication-title: J Dermatol doi: 10.1111/j.1346-8138.2002.tb00285.x contributor: fullname: Kurtoglu – ident: CR4 – ident: CR2 – volume: 55 start-page: 1151 year: 2016 end-page: 1153 ident: CR29 article-title: Our experience with a severe case of aplasia cutis congenita with a large skull defect publication-title: Int J Dermatol doi: 10.1111/ijd.13008 contributor: fullname: Garrow – ident: CR12 – ident: CR30 – volume: 38 issue: 2 year: 2003 ident: CR6 article-title: Aplasia cutis cerebri with partial acrania total reconstruction in a severe case and review of the literature publication-title: J Pediatr Surg doi: 10.1053/jpsu.2003.50064 contributor: fullname: Pal – volume: 13 start-page: 497 year: 2002 end-page: 500 ident: CR22 article-title: Complete osseous regeneration of a large skull defect in a patient with cutis aplasia a conservative approach publication-title: J Craniofac Surg doi: 10.1097/00001665-200207000-00003 contributor: fullname: Muraszko – volume: 53 start-page: 619 issue: 7 year: 2000 end-page: 622 ident: CR20 article-title: Large scalp and skull defect in publication-title: Br J Plast Surg doi: 10.1054/bjps.2000.3406 contributor: fullname: Yang – volume: 110 start-page: 615 year: 1974 end-page: 618 ident: CR10 article-title: Bitemporal aplasia cutis congenita. Occurrence with other cutaneous abnormalities publication-title: Arch Dermatol doi: 10.1001/archderm.1974.01630100071018 contributor: fullname: SchwartzW – volume: 27 start-page: 540 year: 2010 end-page: 542 ident: CR19 article-title: A case of extensive aplasia cutis congenita: a conservative approach publication-title: Pediatr Dermatol doi: 10.1111/j.1525-1470.2010.01266.x contributor: fullname: SepecMP – volume: 28 start-page: e154 issue: 2 year: 2017 end-page: e158 ident: CR8 article-title: Conservative treatment of large aplasia cutis congenita of the scalp with bone defect with basic fibroblast growth factor application publication-title: J Craniofac Surg doi: 10.1097/SCS.0000000000003347 contributor: fullname: Mizuno – volume: 11 start-page: 243 year: 2015 end-page: 248 ident: CR13 article-title: Fatal superior sagittal sinus hemorrhage as a complication of aplasia cutis congenita a case report and literature review publication-title: Forensic Sci Med Pathol doi: 10.1007/s12024-014-9645-5 contributor: fullname: Cohen – volume: 55 start-page: 707 issue: 8 year: 2002 end-page: 708 ident: CR21 article-title: Management of aplasia cutis congenita of the scalp: a continuing enigma publication-title: Br J Plast Surg doi: 10.1054/bjps.2002.3963 contributor: fullname: Saraiya – volume: 9 year: 2021 ident: CR16 article-title: Isolated aplasia cutis congenita: a report of two cases publication-title: Clin Case Rep doi: 10.1002/ccr3.4671 contributor: fullname: Luo – volume: 26 start-page: 273 issue: 9 year: 2014 end-page: 279 ident: CR17 article-title: Combined conservative and surgical management for aplasia cutis congenita a case report and review of the literature publication-title: Wounds contributor: fullname: Li – volume: 14 start-page: 646 year: 1986 end-page: 660 ident: CR11 article-title: Aplasia cutis congenita: a clinical review and proposal for classification publication-title: J Am Acad Dermatol doi: 10.1016/S0190-9622(86)70082-0 contributor: fullname: Frieden – volume: 29 start-page: 582 year: 2009 end-page: 584 ident: CR25 article-title: A case of extensive aplasia cutis congenitawithunderlyingskull defect and central nervous system malformation: discussion of large skin defects, complications, treatment and outcome publication-title: J Perinatol doi: 10.1038/jp.2008.250 contributor: fullname: Morrell – volume: 13 start-page: 513 year: 2002 end-page: 519 ident: CR3 article-title: Surgical treatment of aplasia cutis congenita of the scalp associated with bilateral coronal synostosis publication-title: J Craniofac Surg doi: 10.1097/00001665-200207000-00007 contributor: fullname: Seno – volume: 13 start-page: 125 issue: 2 year: 2003 end-page: 129 ident: CR23 article-title: Treatment dilemma conservative versus surgery in cutis aplasia congenita publication-title: Eur J Pediatr Surg doi: 10.1055/s-2003-39562 contributor: fullname: Al Najjadah – volume: 25 start-page: 861 year: 1933 end-page: 873 ident: CR9 article-title: Congenital defects of the scalp; studies in pathology of development publication-title: Am J Obstet Gynecol doi: 10.1016/S0002-9378(16)41979-4 contributor: fullname: Ingall – ident: CR31 – volume: 9 issue: 6 year: 2013 ident: CR7 article-title: BMS1 is mutated in aplasia cutis congenita publication-title: PLoS Genet doi: 10.1371/journal.pgen.1003573 contributor: fullname: Marneros – volume: 26 start-page: 275 year: 2015 end-page: 277 ident: CR27 article-title: Successful conservative management of a large congenital scalp and skull defect publication-title: J Craniofac Surg doi: 10.1097/SCS.0000000000001798 contributor: fullname: Funayama – ident: CR5 – volume: 8 start-page: 273 issue: 1 year: 2017 end-page: 278 ident: CR14 article-title: Aplasia cutis congenita two case reports and discussion of the literature publication-title: Surg Neurol Int doi: 10.4103/sni.sni_188_17 contributor: fullname: Sotirios – volume: 18 start-page: 427 year: 2007 end-page: 429 ident: CR24 article-title: Aplasia cutis congenita of the scalp and calvarium: conservative wound management with novel wound dressing materials publication-title: J Craniofac Surg doi: 10.1097/01.scs.0000246500.84935.4f contributor: fullname: Sari – volume: 75 start-page: 220 year: 2014 end-page: 223 ident: CR26 article-title: Conservative healing of an 11 _ 9-cm aplasia cutis congenita of the scalp with bone defect publication-title: J Neurol Surg Rep doi: 10.1055/s-0034-1387195 contributor: fullname: Kolby – volume: 83 start-page: 341 year: 2015 ident: 6190_CR28 publication-title: An Pediatr (Barc) doi: 10.1016/j.anpede.2015.09.010 contributor: fullname: JE Betancourth-Alvarenga – volume: 8 start-page: 273 issue: 1 year: 2017 ident: 6190_CR14 publication-title: Surg Neurol Int doi: 10.4103/sni.sni_188_17 contributor: fullname: B Alexondros – volume: 28 start-page: e154 issue: 2 year: 2017 ident: 6190_CR8 publication-title: J Craniofac Surg doi: 10.1097/SCS.0000000000003347 contributor: fullname: D Orgun – ident: 6190_CR31 doi: 10.46900/apn.v4i1(January-April).109 – volume: 13 start-page: 497 year: 2002 ident: 6190_CR22 publication-title: J Craniofac Surg doi: 10.1097/00001665-200207000-00003 contributor: fullname: ST Rhee – ident: 6190_CR12 doi: 10.1159/000442989 – volume: 18 start-page: 427 year: 2007 ident: 6190_CR24 publication-title: J Craniofac Surg doi: 10.1097/01.scs.0000246500.84935.4f contributor: fullname: Y Basterzi – volume: 53 start-page: 619 issue: 7 year: 2000 ident: 6190_CR20 publication-title: Br J Plast Surg doi: 10.1054/bjps.2000.3406 contributor: fullname: JY Yang – volume: 13 start-page: 513 year: 2002 ident: 6190_CR3 publication-title: J Craniofac Surg doi: 10.1097/00001665-200207000-00007 contributor: fullname: Y Komuro – volume: 26 start-page: 273 issue: 9 year: 2014 ident: 6190_CR17 publication-title: Wounds contributor: fullname: F Kuang – volume: 110 start-page: 615 year: 1974 ident: 6190_CR10 publication-title: Arch Dermatol doi: 10.1001/archderm.1974.01630100071018 contributor: fullname: RI Rudolph – volume: 75 start-page: 220 year: 2014 ident: 6190_CR26 publication-title: J Neurol Surg Rep doi: 10.1055/s-0034-1387195 contributor: fullname: V Frojd – volume: 29 start-page: 376 issue: 6 year: 2002 ident: 6190_CR1 publication-title: J Dermatol doi: 10.1111/j.1346-8138.2002.tb00285.x contributor: fullname: H Caksen – ident: 6190_CR5 doi: 10.1001/archderm.141.5.554 – volume: 13 start-page: 125 issue: 2 year: 2003 ident: 6190_CR23 publication-title: Eur J Pediatr Surg doi: 10.1055/s-2003-39562 contributor: fullname: RL Bang – volume: 55 start-page: 707 issue: 8 year: 2002 ident: 6190_CR21 publication-title: Br J Plast Surg doi: 10.1054/bjps.2002.3963 contributor: fullname: HA Saraiya – volume: 55 start-page: 1151 year: 2016 ident: 6190_CR29 publication-title: Int J Dermatol doi: 10.1111/ijd.13008 contributor: fullname: S Puvabanditsin – ident: 6190_CR30 doi: 10.1097/SCS.0000000000002610 – volume: 25 start-page: 861 year: 1933 ident: 6190_CR9 publication-title: Am J Obstet Gynecol doi: 10.1016/S0002-9378(16)41979-4 contributor: fullname: NW Ingall – volume: 5 start-page: 172 issue: 4 year: 2020 ident: 6190_CR15 publication-title: J Obstet Gynecol Cancer Res doi: 10.30699/jogcr.5.4.172 contributor: fullname: H Sohrabi – volume: 9 issue: 6 year: 2013 ident: 6190_CR7 publication-title: PLoS Genet doi: 10.1371/journal.pgen.1003573 contributor: fullname: AG Marneros – volume: 14 start-page: 646 year: 1986 ident: 6190_CR11 publication-title: J Am Acad Dermatol doi: 10.1016/S0190-9622(86)70082-0 contributor: fullname: IJ Frieden – volume: 11 start-page: 243 year: 2015 ident: 6190_CR13 publication-title: Forensic Sci Med Pathol doi: 10.1007/s12024-014-9645-5 contributor: fullname: R Johnson – volume: 29 start-page: 582 year: 2009 ident: 6190_CR25 publication-title: J Perinatol doi: 10.1038/jp.2008.250 contributor: fullname: A Burkhead – ident: 6190_CR4 doi: 10.1007/s00381-002-0654-4 – ident: 6190_CR2 doi: 10.1155/2016/4264721 – volume: 9 year: 2021 ident: 6190_CR16 publication-title: Clin Case Rep doi: 10.1002/ccr3.4671 contributor: fullname: Y Wu – volume: 26 start-page: 275 year: 2015 ident: 6190_CR27 publication-title: J Craniofac Surg doi: 10.1097/SCS.0000000000001798 contributor: fullname: T Maeda – ident: 6190_CR18 doi: 10.1002/ccr3.361 – volume: 27 start-page: 540 year: 2010 ident: 6190_CR19 publication-title: Pediatr Dermatol doi: 10.1111/j.1525-1470.2010.01266.x contributor: fullname: M Starcevic – volume: 38 issue: 2 year: 2003 ident: 6190_CR6 publication-title: J Pediatr Surg doi: 10.1053/jpsu.2003.50064 contributor: fullname: M Bajpai |
SSID | ssj0015829 |
Score | 2.432567 |
SecondaryResourceType | review_article |
Snippet | Background
Aplasia cutis congenita (ACC) of the vertex with bone defect is a rare and begnin anomaly that can involve the epidermis, dermis, and subcutaneous... Aplasia cutis congenita (ACC) of the vertex with bone defect is a rare and begnin anomaly that can involve the epidermis, dermis, and subcutaneous tissues of... BACKGROUNDAplasia cutis congenita (ACC) of the vertex with bone defect is a rare and begnin anomaly that can involve the epidermis, dermis, and subcutaneous... |
SourceID | proquest crossref pubmed springer |
SourceType | Aggregation Database Index Database Publisher |
StartPage | 285 |
SubjectTerms | Case-based Review Medicine Medicine & Public Health Neurosciences Neurosurgery |
Title | Large aplasia cutis congenita of the vertex conservative management |
URI | https://link.springer.com/article/10.1007/s00381-023-06190-x https://www.ncbi.nlm.nih.gov/pubmed/37865964 https://search.proquest.com/docview/2880821500 |
Volume | 40 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://sdu.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1dS8MwFL3oBuKL3x_1iwi-aaRLlqZ9HHNjyPRFBd9C0qYgYjfsJvv53qRdQRRBX0NJy8lp7kluci7AhcaoLXmaUVQPhuIsmVPkTUxtwmzm_GOYN9IePcj75_hm4GxyeLN1UbxeLzOSfqJu7rr5nBbFEOOKESQhReHYxtgjkNzt3uB2NG6SByL2xclcNKcSSVrflfm5l6_x6JvI_JYg9XFnuPmvL96CjVpmkl7Fi21YscUOrN3VifRd6I_dCXCip_4WJUmRfiXBpTHS6WWmySQnKAyJq9VsF6693rv9sOStOS-zB0_DwWN_ROt6CjTlXTmjTHe4d2NhmeSRzbkUOgt1KpjQUdbl2Ma15ZHGNUjH5NIkguVWJqjSjGUm5PvQKiaFPQRiOpoL5y2Hyw0UVKkRBlHXNhRZaJiRAVwuUVXTyjZDNQbJHheFuCiPi1oEcL4EXiG7XcpCF3YyLxXD6SXGQQ7DAA6qEWn64zKORBJ1A7ha4q_qH7D85WVHf3v8GNYZ6pjqoPYJtGbvc3sKq2U2P6t59wkmrM80 |
link.rule.ids | 315,782,786,27933,27934,41073,42142,48344,48347,49649,49652,52153 |
linkProvider | Springer Nature |
linkToHtml | http://sdu.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1LS8QwEB7UBfXi-1GfEbxpoJs0TXsU3XUXVy-u4C0kbQoe3BV3V_bnO0kfIIqg11DSMv0686Uz8w3AucaoLXmWU2QPhqKXLCjiJqE2ZTZ3-jHMC2n3HuXDc3LTcTI5Ud0L46vd65Sk99RNs5tPalGMMW4aQRpSZI6tKI0jxHLrqj-87TbZA5H46WQunFOJKK2aZX7e5WtA-sYyv2VIfeDprv_vkTdgrSKa5KpExiYs2NEWLN9XqfRtuB64GnCi33wfJckQgBOCh2ME1MtUk3FBkBoSN63Zzt169ff2w5LXpmJmB566neF1j1YTFWjGIzmlTLe512NhueSxLbgUOg91JpjQcR5xXOPa8ljjKaRtCmlSwQorU-RpxjIT8l1YGo1Hdh-IaWsunLocHjiQUmVGGDS7tqHIQ8OMDOCiNqt6K4UzVCOR7O2i0C7K20XNAzirLa8Q3y5poUd2PJsohg4mQV4ShgHsla-k2Y_LJBaIgAAua_ur6hOc_HKzg79dfgorveH9QA36D3eHsMqQ1ZRl20ewNH2f2WNYnOSzkwqEn69h0yQ |
linkToPdf | http://sdu.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwpV3dS8MwED_UwfDF74_5GcE3DeuSpWkfxz6YOkVQwbeQtCn4YDfcJv75XtKuIIogvpaSlrtfc7_07n4HcK4xakuepBTZg6G4S2YUcRNRGzObOv0Y5oW0hw_y7jnq9Z1MTtXF76vdFynJoqfBqTTls-YkzZpV45tPcFGMN24yQRxQZJG1Np5kEOm1Tv96OKoyCSLyk8pcaKcSEVs2zvy8ytfg9I1xfsuW-iA0WP__62_AWklASadAzCYs2XwL6rdlin0buiNXG070xPdXkgSBOSW4PALtZabJOCNIGYmb4mw_3PXyr-67Ja9VJc0OPA36j90hLSct0IS35Ywy3eJep4Wlkoc241LoNNCJYEKHaZvjNa4tDzWeTlomkyYWLLMyRv5mLDMB34WVfJzbfSCmpblwqnN4EEGqlRhh0AXaBiINDDOyARcLE6tJIaihKulkbxeFdlHeLuqjAWcLLyjEvUtm6NyO51PFcOOJkK8EQQP2CvdU63EZhSIO2w24XPhClZ_m9JeHHfzt9lOo3_cGanR1d3MIqwzJTlHNfQQrs7e5PYblaTo_KfH4CZtZ2-c |
openUrl | ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Large+aplasia+cutis+congenita+of+the+vertex+conservative+management&rft.jtitle=Child%27s+nervous+system&rft.au=Bouali%2C+Sofiene&rft.au=Charfeddine%2C+Sarah+Houimli&rft.au=Ghedira%2C+Khalil&rft.au=Mechergui%2C+Haifa&rft.date=2024-02-01&rft.pub=Springer+Berlin+Heidelberg&rft.issn=0256-7040&rft.eissn=1433-0350&rft.volume=40&rft.issue=2&rft.spage=285&rft.epage=292&rft_id=info:doi/10.1007%2Fs00381-023-06190-x&rft.externalDocID=10_1007_s00381_023_06190_x |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0256-7040&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0256-7040&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0256-7040&client=summon |