Abstract
A 39-year old man came to our outpatient clinic with long history of unspecific symptoms and signs. Cerebral MRI showed herniation of the cerebellar tonsils of more than 1 cm below the foramen magnum and a triventricular hydrocephalus. A diagnosis of Chiari I malformation was retained. After an osteo-dural decompression of the posterior fossa, post-operative MRI revealed an aqueductal stenosis with triventricular hydrocephalus. An endoscopic-third- ventriculostomy showed an idiopathic stenosis of the right foramen of Monro. Residual symptoms and persistence of biventricular hydrocephalus justified a ventriculo-peritoneal shunt. Aqueductal and foramina of Monro stenosis can mimick a Chiari I malformation.
References
Alexander E Jr, Bottarell EH (1949) Unilateral hydrocephalus resulting from occlusion of foramen of Monro. Complication of radical removal of brain abscess. J Neurosurg 6:197–206
Arienta C, Capricci E, Baiguini M (1986) Non tumoral aqueduct stenosis. Multiple microscopic subependymal glial protuberances demonstrated at histological examination. J Neurosurg Sci 30:67–70
Balestrazzi P, de Gressi S, Donadio A, Lenzini S (1989) Periaqueductal gliosis causing hydrocephalus in a patient with neurofibromatosis type 1. Neurofibromatosis 2:322–325
Caldarelli M, Novegno F, Di Rocco C (2009) A late complication of CSF shunting: acquired Chiari I malformation. Childs Nerv Syst 25(4):443–445
Clatterbuck RE, Sipos EP (1997) The efficient calculation of neurosurgically relevant volumes from computed tomographic scans using Cavalieri’s direct estimator. Neurosurgery 40:339–343
Dandy W (1920) The diagnosis and treatment of hydrocephalus resulting from strictures of the aqueduct of Sylvius. Surg Gynaecol Obstet 31:340–358
Huang PP, Constantini S (1994) “Acquired Chiari I malformation”. Case report (1994). J Neurosurg 80:1099–1102
Kalhorn SP, Strom RG, Harter DH (2011) Idiopathic bilateral stenosis of the foramina of Monro treated using endoscopic foraminoplasty and septostomy. Neurosurg Focus 30(4):E5
Levine DN (2008) Intracranial pressure and ventricular expansion in hydrocephalus: have we been asking the wrong question? J Neurol Sci 269:1–11
Mangano FT, McAllister JP, Jones HC, Johnson MJ, Kriebel RM (1998) The microglial response to progressive hydrocephalus in a model of inherited aqueductal stenosis. Neurol Res 20:697–704
Mayhew TM, Olsen DR (1991) Magnetic resonance imaging (MRI) and model free estimates of brain volume determined using the Cavalieri principle. J Anat 178:133–144
Milhorat TH, Chou MW, Trinidad EM, Kula RW, Mandell M, Wolpert C, Speer MC (1999) Chiari I malformation redefined: clinical and radiographic findings for 364 symptomatic patients. Neurosurg 44:1005–1017
Novegno F, Caldarelli M, Massa A, Chieffo D, Massimi L, Pettorini B, Tamburrini G, Di Rocco C (2008) The natural history of the Chiari type I anomaly. J Neurosurg Pediatr 2:179–187
Payner TD, Prenger E, Berger TS, Crone KR (1994) Acquired Chiari malformations: incidence, diagnosis, and management. Neurosurg 34(3):429–434
Pfeiffer G, Friede RL (1984) Unilateral hydrocephalus from early developmental occlusion of one foramen of Monro. Acta Neuropathol 64:75–77
Rose GD, Harry JD (1990) Brain volume estimation from serial section measurements: a comparison of methodologies. J Neurosci Methods 35:115–124
Seiler FA, Lew SM (2010) Aqueductal stenosis presenting as isolated tremor: case report and review of the literature. Ped Neurosurg 46:392–395
Sathi S, Stieg PE (1993) “Acquired” Chiari I malformation after multiple lumbar punctures: case report. Neurosurg 32:306–309
Tisell M (2005) How should primary aqueductal stenosis in adults be treated? — A review. Acta Neurol Scand 111:145–153
Tubbs RS, Lyerly MJ, Loukas M, Shoja MM, Oakes WJ (2007) The pediatric Chiari I malformation: a review. Childs Nerv Syst 23:1239–1250
Wilberger JE Jr, Vertosick FT Jr, Vries JK (1983) Unilateral hydrocephalus secondary to congenital atresia of the foramen of Monro. J Neurosurg 59(5):899–901
Massimi L, Pravatà E, Tamburrini G, Gaudino S, Pettorini B, Novegno F, Colosimo C Jr, Di Rocco C (2011) Endoscopic third ventriculostomy for the management of Chiari I and related hydrocephalus: outcome and pathogenetic implications. Neurosurg 68(4):950–956
Conflicts of interest
None
Author information
Authors and Affiliations
Corresponding author
Additional information
Comment
In this paper, the authors report an intriguing case of a Chiari malformation type I associated with a stenosis of bilateral foramina Monroi, which was misdiagnosed before surgery. The authors suppose that a high pressure gradient between the lateral ventricles and the third ventricle is the cause of the deformity of the third ventricle. In fact, to my knowledge, no enquiries have been published on the pressure gradient inside the ventricular system in obstructive hydrocephalus. The case is attractive and may support our observations of other cases of Chiari malformation with postoperative CSF flow dysregulation. This can be reasonably explained by a hidden obstructive hydrocephalus and confirms the hypothesis, that the Chiari malformation should be assimilated to a CSF flow impairment. Research studies should be performed in order to gain more insight into the pathophysiology of these pathologies.
Alex Alfieri
Sebastian Simmermacher
Gershom Koman
Halle (Saale), Germany
Rights and permissions
About this article
Cite this article
Bartoli, A., Ghinda, C.D., Radovanovic, I. et al. Hidden aqueductal stenosis associated to bilateral idiopathic foramina of Monro stenosis mimicking a Chiari I malformation? Case report. Acta Neurochir 154, 2109–2113 (2012). https://doi.org/10.1007/s00701-012-1438-6
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s00701-012-1438-6