Management of Coincident Metopic and Unilateral Lambdoid Craniosynostosis, a Rare Entity

被引:0
|
作者
Daly, Gwendolyn E. [1 ]
Ferry, Andrew M. [1 ]
Howell, Lori K. [1 ]
Selden, Nathan R.
Wolfswinkel, Erik M. [1 ]
机构
[1] Oregon Hlth & Sci Univ, Portland, OR USA
来源
FACE | 2024年 / 5卷 / 04期
关键词
craniosynostosis; metopic synostosis; unilateral lambdoid synostosis; fronto-orbital advancement; open posterior cranial vault remodeling; multi-suture craniosynostosis; CRANIAL VAULT DISTRACTION; POSTERIOR; EXPANSION;
D O I
10.1177/27325016241268569
中图分类号
R61 [外科手术学];
学科分类号
摘要
Introduction: Multi-suture craniosynostosis is rare and comprises only 3% to 7% of all craniosynostosis cases. Depending on the sutures involved, there are multiple operative approaches for this disease. In this report, we describe the staged surgical management of a patient who presented with metopic and unilateral lambdoid synostosis with initial posterior cranial vault remodeling followed by fronto-orbital advancement (FOA).Methods: At our institution, case reports detailing a single patient are not considered human research by the Institutional Review Board and official approval was not sought. Written consent for inclusion of patient information and images was obtained from the patient's legally authorized representative.Results: A male patient was treated for metopic and right unilateral lambdoid synostosis. Physical examination was notable for trigonocephaly, right sided posterior plagiocephaly, right mastoid bulging, and contralateral parietal bossing. Treatment of his synostotic deformities was delayed and treated in stages. This was achieved with initial posterior vault expansion, to treat his lambdoid synostosis, via a modification to the classic switch cranioplasty at 5 months of age. The patient subsequently underwent fronto-orbital advancement for correction of metopic synostosis at 10 months of age. The posterior cranial vault remodeling procedure permitted sufficient cranial vault expansion to delay fronto-orbital advancement until 10 months of age. Of note, excellent bone fill and union were observed of the posterior bone grafts at the time of scalp flap elevation during this second procedure. His most recent follow up appointment at 11 months status post FOA demonstrated continued deformational correction as well as good bone fill and wound healing.Conclusions: Multi-suture craniosynostosis is rare with only a single other report in the literature discussing concurrent metopic and unilateral lambdoid synostosis. A multi-stage approach is the most commonly employed technique and must be tailored to each patients' unique presentation.
引用
收藏
页码:614 / 619
页数:6
相关论文
共 50 条
  • [41] Serous cystadenocarcinoma of the pancreas - Management of a rare entity
    Friebe, V
    Keck, T
    Mattern, D
    Schmitt-Graeff, A
    Werner, M
    Mikami, Y
    Adam, U
    Hopt, UT
    PANCREAS, 2005, 31 (02) : 182 - 187
  • [42] Anaesthetic management of foetus in foetu: A rare entity
    Khatavkar, Sonal S.
    Kabeer, Waseema
    Ghodake, Ashwini P.
    Shah, Krusha S.
    INDIAN JOURNAL OF ANAESTHESIA, 2023, 67 : S68 - S69
  • [43] Sigmoid Volvulus: Diagnosis and Management of a Rare Entity
    Bhattacharya, Sumona
    Skole, Kevin
    AMERICAN JOURNAL OF GASTROENTEROLOGY, 2017, 112 : S785 - S785
  • [44] Management of an Unusual Maxillary Canine: A Rare Entity
    Muppalla, Jaya Nagendra Krishna
    Kavuda, Krishnamurthy
    Punna, Rajani
    Vanapatla, Amulya
    CASE REPORTS IN DENTISTRY, 2015, 2015
  • [45] Surgical Management of Complex Syndromic Craniosynostosis: Experience With a Rare Genetic Variant
    Celie, Karel-Bart
    Yuan, Melissa
    Hoffman, Caitlin
    O'Connor, Ashley
    Bogue, Jarrod
    Imahiyerobo, Thomas
    JOURNAL OF CRANIOFACIAL SURGERY, 2020, 31 (01) : 294 - 299
  • [46] Anesthetic management of a rare case of Shprintzen-Goldberg craniosynostosis syndrome
    Gupta, Arun Kumar
    Divekar, Devdas S.
    Shah, Bhawini
    Dhulkhed, Vithal K.
    PEDIATRIC ANESTHESIA, 2010, 20 (08) : 771 - 773
  • [47] Status dystonicus: Diagnosis and management of a rare and challenging entity
    Thakkar, Prince
    Naveen, B. P.
    Yoganathan, Sangeetha
    John, Judy Ann
    Thomas, Maya
    JOURNAL OF PEDIATRIC REHABILITATION MEDICINE, 2019, 12 (01) : 71 - 74
  • [48] CRANIAL ANGIOSARCOMA: SUCCESSFUL MULTIDISCIPLINARY MANAGEMENT OF THIS RARE ENTITY
    Guthikonda, Bharat
    Thakur, Jai
    Khan, Imad
    Ahmed, Osama
    Shorter, Cedric
    Wilson, Jon
    Welsh, James
    Cuellar, Hugo
    Jeroudi, Majed
    NEURO-ONCOLOGY, 2011, 13 : 163 - 163
  • [49] Anal Adenocarcinoma: A Rare Entity in Need of Multidisciplinary Management
    Lukovic, Jelena
    Kim, J. John
    Liu, Zhihui Amy
    Cummings, Bernard J.
    Brierley, James D.
    Wong, Rebecca K. S.
    Ringash, Jolie G.
    Dawson, Laura A.
    Barry, Aisling
    Krzyzanowska, Monika K.
    Chen, Eric X.
    Hedley, David W.
    Quereshy, Fayez A.
    Swallow, Carol J.
    Gryfe, Robert N.
    Kennedy, Erin D.
    Easson, Alexandra M.
    Hosni, Ali
    DISEASES OF THE COLON & RECTUM, 2022, 65 (02) : 189 - 197
  • [50] Management of the rare entity of primary pancreatic cystic neoplasms
    Stamatakos, Michael
    Sargedi, Constantina
    Angelousi, Anna
    Kontzoglou, Konstantinos
    Safioleas, Panagiotis
    Petropoulou, Constantina
    Safioleas, Michael
    JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY, 2009, 24 (07) : 1203 - 1210