Delayed otogenic hydrocephalus after acute otitis media in pediatric patients: the changing presentation of a serious otologic complication.
Details
Serval ID
serval:BIB_21DF2EA0CD73
Type
Article: article from journal or magazin.
Publication sub-type
Case report (case report): feedback on an observation with a short commentary.
Collection
Publications
Institution
Title
Delayed otogenic hydrocephalus after acute otitis media in pediatric patients: the changing presentation of a serious otologic complication.
Journal
Acta Oto-laryngologica
ISSN
0001-6489 (Print)
ISSN-L
0001-6489
Publication state
Published
Issued date
2005
Volume
125
Number
11
Pages
1230-1235
Language
english
Notes
Publication types: Case Reports ; Journal ArticlePublication Status: ppublish
Abstract
CONCLUSIONS: The clinical presentation of otogenic dural sinus thrombosis (DST) as a complication of acute otitis media (AOM) can be masked by antibiotic treatment. Morning episodes of vomiting and/or headache, visual impairment and a history of AOM seem to be indicative of otogenic hydrocephalus. We therefore advocate that the MRI scans of patients with similar symptoms should be carefully studied to facilitate the early diagnosis of a potentially life-threatening complication.
OBJECTIVE: To describe the frequency, pathognomonic signs, clinical course and outcome of otogenic hydrocephalus and DST as complications of AOM in pediatric patients.
MATERIAL AND METHODS: We undertook a retrospective chart review of all pediatric patients (age 1-14 years) treated for otitis media and its complications at an academic medical center between 1999 and 2003. The main outcome measures were otologic and ophthalmologic findings and CT and MRI scans at the beginning of treatment and 3 months later.
RESULTS: We report on five cases with otogenic DST following AOM. All but one of them presented initially with diplopia caused by otogenic hydrocephalus. In four cases the otologic complaints had already disappeared by the time of MRI confirmation of the diagnosis. Only one child was referred with severe otologic symptoms. Management included systemic antibiotics, short-term heparin anticoagulation and surgical decompression. In our cases, even after intensive i.v. antibiotic treatment, only surgery led to a significant improvement in the clinical condition.
OBJECTIVE: To describe the frequency, pathognomonic signs, clinical course and outcome of otogenic hydrocephalus and DST as complications of AOM in pediatric patients.
MATERIAL AND METHODS: We undertook a retrospective chart review of all pediatric patients (age 1-14 years) treated for otitis media and its complications at an academic medical center between 1999 and 2003. The main outcome measures were otologic and ophthalmologic findings and CT and MRI scans at the beginning of treatment and 3 months later.
RESULTS: We report on five cases with otogenic DST following AOM. All but one of them presented initially with diplopia caused by otogenic hydrocephalus. In four cases the otologic complaints had already disappeared by the time of MRI confirmation of the diagnosis. Only one child was referred with severe otologic symptoms. Management included systemic antibiotics, short-term heparin anticoagulation and surgical decompression. In our cases, even after intensive i.v. antibiotic treatment, only surgery led to a significant improvement in the clinical condition.
Keywords
Acute Disease, Adolescent, Anti-Bacterial Agents/adverse effects, Anti-Bacterial Agents/therapeutic use, Child, Child, Preschool, Cross-Sectional Studies, Diagnosis, Differential, Early Diagnosis, Follow-Up Studies, Haemophilus Infections/complications, Haemophilus Infections/drug therapy, Humans, Hydrocephalus/diagnosis, Hydrocephalus/etiology, Infant, Magnetic Resonance Imaging, Mastoiditis/diagnosis, Mastoiditis/etiology, Otitis Media/complications, Otitis Media/drug therapy, Retrospective Studies, Sinus Thrombosis, Intracranial/diagnosis, Sinus Thrombosis, Intracranial/etiology, Survival Analysis, Tomography, X-Ray Computed
Pubmed
Web of science
Create date
21/01/2013 14:29
Last modification date
20/08/2019 12:58