Document Detail


Mild trigonocephaly with clinical symptoms: analysis of surgical results in 65 patients.
MedLine Citation:
PMID:  12042920     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
INTRODUCTION: It has been believed that isolated, mild trigonocephaly rarely presents with clinical symptoms. PATIENTS AND METHODS: We diagnosed and operated on 65 patients with mild trigonocephaly and developmental delay up to July 2000. There were 47 boys and 18 girls in our series. All patients had symptoms such as delay in language development, hyperactivity, autistic tendencies, and motor dysfunctions. Their facial features were characterized by a metopic ridge, depressed temples, heel-shaped rather than keel-shaped forehead, and slight hypotelorism. The most important physical sign was the palpable metopic ridge. Most patients did not exhibit any symptoms until they were more than 1 year old. Fifteen patients showed regression in language acquisition and use. Three-dimensional computed tomography revealed the metopic ridge, depressed pterional regions, hypotelorism, and small anterior fossae. Magnetic resonance imaging was performed on all patients and demonstrated no abnormal findings in the brain. Single-photon emission computed tomography (SPECT) was performed on 83% of patients and revealed decreased cerebral blood flow (CBF) in the frontal lobes of 76% of those patients. Decompressive cranioplasty of the frontal bone involving the skull base was performed on all patients. RESULTS: In most (61 out of 65) patients a degree of postoperative improvement in clinical symptoms was noted, especially in behavioral problems. Postoperative SPECT demonstrated increased CBF in the frontal lobes in 95% of the patients. CONCLUSION: Based on these results, it can be postulated that mild trigonocephaly is frequently associated with developmental delays and that these symptoms can be improved to a certain degree by decompressive cranioplasty.
Authors:
Takeyoshi Shimoji; Satoshi Shimabukuro; Seiichi Sugama; Yasuo Ochiai
Publication Detail:
Type:  Journal Article     Date:  2002-05-07
Journal Detail:
Title:  Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery     Volume:  18     ISSN:  0256-7040     ISO Abbreviation:  Childs Nerv Syst     Publication Date:  2002 May 
Date Detail:
Created Date:  2002-06-03     Completed Date:  2002-10-09     Revised Date:  2004-11-17    
Medline Journal Info:
Nlm Unique ID:  8503227     Medline TA:  Childs Nerv Syst     Country:  Germany    
Other Details:
Languages:  eng     Pagination:  215-24     Citation Subset:  IM    
Affiliation:
Department of Neurosurgery, Okinawa Naha Prefectural Hospital, 1-3-1 Yogi, Naha City, Japan. simoji_takeyosi@hosp.pref.okinawa.jp
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
Child
Child, Preschool
Craniofacial Abnormalities / complications,  physiopathology,  surgery*
Craniotomy
Developmental Disabilities / diagnosis,  etiology*,  physiopathology
Female
Frontal Lobe / blood supply
Humans
Magnetic Resonance Imaging
Male
Severity of Illness Index
Tomography, Emission-Computed, Single-Photon
Comments/Corrections
Comment In:
Childs Nerv Syst. 2002 Dec;18(12):659-60; author reply 661-2   [PMID:  12483347 ]

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


Previous Document:  New non-invasive sonographic modality for intracranial pressure/volume monitoring.
Next Document:  Astrocytomas of the cerebral peduncle in children: surgical experience in seven patients.