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A Case of Bilateral Lambdoid and Sagittal Synostosis Diagnosed with Skull Fracture after Vacuum-assisted Delivery: A Case Report and Literature Review.
Nakamura, Natsuki; Harada, Atsuko; Maeno, Kazushige; Kyutoku, Shigeo; Ueda, Koichi.
Affiliation
  • Nakamura N; Department of Pediatric Neurosurgery, Takatsuki General Hospital, Takatsuki, Osaka, Japan.
  • Harada A; Department of Pediatric Neurosurgery, Takatsuki General Hospital, Takatsuki, Osaka, Japan.
  • Maeno K; Department of Neurosurgery, Takatsuki General Hospital, Takatsuki, Osaka, Japan.
  • Kyutoku S; Division of Reconstructive Plastic Surgery, Nara City Hospital, Nara, Nara, Japan.
  • Ueda K; Department of Plastic and Reconstructive Surgery, Osaka Medical and Pharmaceutical University, Takatsuki, Osaka, Japan.
NMC Case Rep J ; 11: 157-161, 2024.
Article in En | MEDLINE | ID: mdl-38974117
ABSTRACT
Craniosynostosis (CS) can develop in the fetal period, but it is difficult to diagnose prenatally. In this case, a 3-month-old female baby developed extensive subgaleal hematoma and severe anemia after vacuum-assisted delivery. Her computed tomography showed bilateral lambdoid and sagittal synostosis (BLSS) with a depressed fracture of the right parietal bone. She was referred to our hospital for treatment of the CS. At 4 months of age, she underwent bilateral lambda and sagittal suturectomy and foramen magnum decompression. CS may result in trauma at delivery, because CS disturbs fetal head molding during delivery and disrupts passage through the birth canal. In particular, the risk of severe peripartum trauma is thought to increase in cases of CS with multiple suture fusions, such as those observed in BLSS, due to the strong inhibition of this process of passage through the birth canal. Therefore, if the delivery is abnormally prolonged or if the infant has a massive subgaleal hematoma, it is important to perform evaluations for CS after birth.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: NMC Case Rep J Year: 2024 Document type: Article Affiliation country: Japan Country of publication: Japan

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: NMC Case Rep J Year: 2024 Document type: Article Affiliation country: Japan Country of publication: Japan