Persistent depression of the lambda site with progressive skull deformity may be a sign of suture closure: Case series and pathological consideration.

brachycephaly craniosynostosis flat head syndrome lambda pathology

Journal

World neurosurgery
ISSN: 1878-8769
Titre abrégé: World Neurosurg
Pays: United States
ID NLM: 101528275

Informations de publication

Date de publication:
02 Jul 2024
Historique:
received: 25 06 2024
accepted: 26 06 2024
medline: 5 7 2024
pubmed: 5 7 2024
entrez: 4 7 2024
Statut: aheadofprint

Résumé

Flat head syndrome (FHS) sometimes occurs when a baby maintains the same head position during the first several months of life causing a skull deformity. FHS usually improves with time and natural growth, however, some shows aggravation against conservative treatment. We reviewed pathologically proved early closure of skull suture that may have seen secondary to FHS. The clinical and radiological findings of the patients who showed progressive skull deformity resembling FHS were retrospectively reviewed. All the patients underwent surgical treatment and pathological specimens were obtained. The detected patients included two 5-month-old infants and one 1-year-old infant. The formers were conservatively treated without any obvious premature suture closure on computed tomography (CT), and later developed progressive tower-like skull deformities. The infants were diagnosed with possible premature fusion of Lambda site and underwent removal around lambda depression (LD). The latter showed evident sagittal suture closure on CT with digital markings, and was diagnosed with increased intracranial pressure and underwent cranioplasty of posterior expansion. Histopathological specimens obtained from the patients' resected sutures showed irregularly narrowed suture structure with ossification and fibrous tissue proliferation within them, supporting the diagnosis of premature closure of the sagittal sutures. Their postoperative courses were uneventful, and their skull deformities subsequently improved. Conservative therapy-resistant progressive occipital skull deformity with LD may be a sign of early suture closure, even if CT does not show obvious suture closure. The findings are helpful for early diagnosis and might lead to minimal invasive surgery if needed.

Identifiants

pubmed: 38964459
pii: S1878-8750(24)01119-7
doi: 10.1016/j.wneu.2024.06.154
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2024 Elsevier Inc. All rights reserved.

Auteurs

Tomohito Nagai (T)

Departments of Neurosurgery, Miyagi Children's Hospital, Sendai, Japan.

Toshiaki Hayashi (T)

Departments of Neurosurgery, Miyagi Children's Hospital, Sendai, Japan. Electronic address: hayashi@miyagi-children.or.jp.

Tomomi Kimiwada (T)

Departments of Neurosurgery, Miyagi Children's Hospital, Sendai, Japan.

Madoka Inukai (M)

Departments of Neurosurgery, Miyagi Children's Hospital, Sendai, Japan.

Junji Takeyama (J)

Departments of Neurosurgery Pathology, Miyagi Children's Hospital, Sendai, Japan.

Yoshihisa Shimanuki (Y)

Departments of Radiology, and Plastic Surgery, Miyagi Children's Hospital, Sendai, Japan.

Masahiro Kitami (M)

Departments of Radiology, and Plastic Surgery, Miyagi Children's Hospital, Sendai, Japan.

Takehiko Sanada (T)

Departments of Plastic Surgery, Miyagi Children's Hospital, Sendai, Japan.

Hidenori Endo (H)

Department of Neurosurgery, Tohoku University Graduate School of Medicine, Sendai, Japan.

Classifications MeSH