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Table of Contents    
LETTER TO EDITOR
Year : 2011  |  Volume : 59  |  Issue : 4  |  Page : 633-634

Spontaneous intracranial hypotension in a patient with classical type Ehlers-Danlos syndrome


1 Department of Neurology, Reinier de Graaf Hospital, Delft, The Netherlands
2 UMC St. Radboud, Nijmegen, The Netherlands

Date of Submission25-May-2011
Date of Decision29-May-2011
Date of Acceptance10-Jul-2011
Date of Web Publication30-Aug-2011

Correspondence Address:
H J Gilhuis
Department of Neurology, Reinier de Graaf Hospital, Delft
The Netherlands
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/0028-3886.84357

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How to cite this article:
Grosveld W, Gilhuis H J, Voermans N C. Spontaneous intracranial hypotension in a patient with classical type Ehlers-Danlos syndrome. Neurol India 2011;59:633-4

How to cite this URL:
Grosveld W, Gilhuis H J, Voermans N C. Spontaneous intracranial hypotension in a patient with classical type Ehlers-Danlos syndrome. Neurol India [serial online] 2011 [cited 2019 Sep 15];59:633-4. Available from: http://www.neurologyindia.com/text.asp?2011/59/4/633/84357


Sir,

A 37-year-old female, a known case of classical type  Ehlers-Danlos syndrome More Details (EDS) developed progressive headache over a period of one month. Headache would occur shortly after assuming an upright position and get relieved on lying down and was associated with nausea, vomiting, and blurred vision. Physical examination revealed typical features of classical type EDS: hyperextensible skin, generalized joint hypermobility, and widened atrophic scars and no neurological deficits. Complete blood picture, blood biochemistry, cerebrospinal fluid (CSF) analysis, and opening pressure of the lumbar puncture were normal. Brain T1-weighted magnetic resonance imaging (MRI) with gadolinium showed diffuse pachymeningeal enhancement [Figure 1]. Radioisotope cisternography identified a CSF leakage at the level of the cervicothoracic junction [Figure 2]. A diagnosis of spontaneous intracranial hypotension (SIH) due to CSF leakage was considered and she was advised bed rest for five days with no effect, after which she was successfully treated with an epidural blood patch at the level of the leakage.
Figure 1: Cerebral T1-weighted MRI with gadolinium showing diffuse meningeal enhancement

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Figure 2: Radioisotope cisternography. Note the CSF leakage at the level of the cervicothoracic junction

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SIH is caused by spinal CSF leakage, which is presumed to be related to an underlying weakness of the spinal meninges. This syndrome presents with a postural headache, which is defined as a headache that occurs within 15 min after assuming an upright position and disappears or improves within 30 min after lying down. [1] In addition to headaches, SIH patients often have a wide variety of additional symptoms like nausea, vomiting, neck stiffness, tinnitus, hypacusia, and photophobia. Diffuse pachymeningeal enhancement after administration of gadolinium is the most characteristic feature on MRI, and confirms the diagnosis. Other typical MRI features include subdural fluid collections, engorgement of venous structures, pituitary hyperemia, and sagging of the brain. Computed tomography myelography or radionuclide cisternography are the imaging modalities to identify the site of the CSF leakage. An epidural blood patch is the mainstay of treatment. [1],[2],[3]

Evidence for an inherited connective tissue disorder such as EDS is found on physical examination in two-thirds of SIH patients. Isolated joint hypermobility is found in two-fifths of these patients. One-fifth of patients have subtle skeletal manifestations of Marfan syndrome without a mutation in fibrillin-1. Less frequently, a well-defined connective tissue disorder such as Marfan syndrome or EDS is found. These findings suggest that patients with inherited connective tissue diseases are more susceptible to SIH due to the generalized fragility of tissues, probably including the meninges. [2],[3] The Marfan syndrome has repeatedly been associated with postural headache due to SIH, mostly in children and young adults. [4],[5] Till date, only two cases of classical type EDS with postural headache due to SIH have been reported. [3] In conclusion, the diagnosis of SIH should be considered in EDS patients with postural headache.

 
  References Top

1.Schievink WI. Spontaneous spinal cerebrospinal fluid leaks and intracranial hypotension: Clinical review. JAMA 2006;295:2286-96.  Back to cited text no. 1
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2.Mokri B, Maher CO, Sencakova D. Spontaneous CSF leaks: Underlying disorder of connective tissue. Neurology 2002;58:814-6.  Back to cited text no. 2
[PUBMED]  [FULLTEXT]  
3.Schievink WI, Gordon OK, Tourje J. Connective tissue disorders with spontaneous spinal cerebrospinal fluid leaks and intracranial hypotension: Prospective study. Neurosurgery 2004;54:65-71.  Back to cited text no. 3
[PUBMED]  [FULLTEXT]  
4.Cheuret E, Edouard T, Mejdoubi M, Acar P, Pienkowski C, Cances C, et al. Intracranial hypotension in a girl with Marfan syndrome: Case report and review of the literature. Childs Nerv Syst 2008;24:509-13.  Back to cited text no. 4
[PUBMED]  [FULLTEXT]  
5.Voermans NC, Dijk KG, Bos MM, Geus-Oei LF, Verrips A, Lindert EJ. Postural headache in Marfan syndrome associated with spinal cysts and liquor hypotension. Neuropediatrics 2009;40:201-4.  Back to cited text no. 5
[PUBMED]  [FULLTEXT]  


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