تقرير
A case report of cerebrospinal fluid leak secondary to inner ear malformation.
| العنوان: | A case report of cerebrospinal fluid leak secondary to inner ear malformation. |
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| المؤلفون: | Ninh TP; Department of Radiology, National Hospital of Pediatrics, Ha Noi, Vietnam., Dinh TQ; Department of General Surgery, Ho Chi Minh City Children's Hospital, Ho Chi Minh City, Vietnam., My TT; Department of Radiology, Hanoi Medical University, Ha Noi, Vietnam., Thao BP; Department of Radiology, Vinmec Times City International Hospital, Ha Noi, Vietnam., Hieu BK; Department of Radiology, National Hospital of Pediatrics, Ha Noi, Vietnam., Bang LV; Department of Pathology, Tam Anh General Hospital, Ha Noi, Vietnam., Duc NM; Department of Radiology, Hanoi Medical University, Ha Noi, Vietnam.; Department of Radiology, Pham Ngoc Thach University of Medicine, Ho Chi Minh City, Vietnam.; Department of Radiology, Children's Hospital 2, Ho Chi Minh City, Vietnam. |
| المصدر: | Radiology case reports [Radiol Case Rep] 2021 Jun 07; Vol. 16 (8), pp. 1931-1933. Date of Electronic Publication: 2021 Jun 07 (Print Publication: 2021). |
| نوع المنشور: | Case Reports |
| اللغة: | English |
| بيانات الدورية: | Publisher: Elsevier Country of Publication: Netherlands NLM ID: 101467888 Publication Model: eCollection Cited Medium: Print ISSN: 1930-0433 (Print) Linking ISSN: 19300433 NLM ISO Abbreviation: Radiol Case Rep Subsets: PubMed not MEDLINE |
| أسماء مطبوعة: | Publication: 2015-: Amsterdam : Elsevier Original Publication: Seattle, WA : University of Washington, 2006- |
| مستخلص: | Spontaneous cerebrospinal fluid (CSF) rhinorrhea is rare and may develop secondary to inner ear malformation. A possible diagnosis of CSF leak should be considered in any pediatric patient who presents with hearing impairment, rhinorrhea, or otorrhea. Temporal bone computed tomography should be performed in children with hearing impairments. We describe a case of congenital inner ear anomaly in a 12-month-old girl who presented with intermittent rhinorrhea after birth and detected hearing problems when she was 6 months. After diagnosis, the CSF leak was surgically repaired without complications. (© 2021 The Authors. Published by Elsevier Inc. on behalf of University of Washington.) |
| References: | J Laryngol Otol. 2005 Sep;119(9):714-8. (PMID: 16156913) Ear Nose Throat J. 2021 Feb;100(1_suppl):38S-41S. (PMID: 32320299) Otolaryngol Head Neck Surg. 1985 Oct;93(5):625-34. (PMID: 3932931) Balkan Med J. 2017 Sep 29;34(5):397-411. (PMID: 28840850) Radiographics. 2012 May-Jun;32(3):683-98. (PMID: 22582354) Laryngoscope. 1987 Mar;97(3 Pt 2 Suppl 40):2-14. (PMID: 3821363) Int J Pediatr Otorhinolaryngol. 2019 Sep;124:147-151. (PMID: 31195308) J Zhejiang Univ Sci B. 2019 Feb.;20(2):156-163. (PMID: 30666849) J Neurol Surg B Skull Base. 2014 Apr;75(2):117-24. (PMID: 24719798) |
| فهرسة مساهمة: | Keywords: Cerebrospinal fluid leak; Cochlear malformation; Congenital deafness; Congenital inner ear malformation |
| تواريخ الأحداث: | Date Created: 20210621 Latest Revision: 20210622 |
| رمز التحديث: | 20240829 |
| مُعرف محوري في PubMed: | PMC8193066 |
| DOI: | 10.1016/j.radcr.2021.04.072 |
| PMID: | 34149977 |
| قاعدة البيانات: | MEDLINE |
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Full Text Finder | تدمد: | 1930-0433 |
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| DOI: | 10.1016/j.radcr.2021.04.072 |