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J Clin Imaging Sci 2012,  2:27

Fahr's disease Presenting with Aneurysmal Subarachnoid Hemorrhage

1 Department of Neurology and Neurosurgery, Montreal Neurological Institute and Hospital, McGill University, Montreal, Quebec, Canada; Department of Neurosurgery, King Fahad University Hospital, University of Dammam, Al-Khobar, Saudi Arabia
2 Department of Neurology and Neurosurgery, Montreal Neurological Institute and Hospital, McGill University, Montreal, Quebec, Canada; Neurosurgery Division, Department of surgery, King Saud University, Riyadh, Saudi Arabia
3 Department of Neurology and Neurosurgery, Montreal Neurological Institute and Hospital, McGill University, Montreal, Quebec, Canada

Date of Submission08-Mar-2012
Date of Acceptance10-Apr-2012
Date of Web Publication23-May-2012

Correspondence Address:
Hosam Al-Jehani
c/o Luisa Birri, 3801 University St., Suite 109, Montreal, QC, H3A 2B4, Canada

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Source of Support: None, Conflict of Interest: None

DOI: 10.4103/2156-7514.96542

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Fahr's disease is a rare disorder of slowly progressive cognitive, psychiatric, and motor decline associated with idiopathic basal ganglia calcification (IBGC) and widespread calcification in the brain and cerebellum. Acute presentation of IBGC is most often as a seizure disorder; however, we present a case of an acute IBCG presentation in which the cause of the deterioration was an aneurysmal subarachnoid hemorrhage.

Keywords: Fahr′s disease, idiopathic basal ganglia calcification, intracranial aneurysm, subarachnoid hemorrhage

How to cite this article:
Al-Jehani H, Ajlan A, Sinclair D. Fahr's disease Presenting with Aneurysmal Subarachnoid Hemorrhage. J Clin Imaging Sci 2012;2:27

How to cite this URL:
Al-Jehani H, Ajlan A, Sinclair D. Fahr's disease Presenting with Aneurysmal Subarachnoid Hemorrhage. J Clin Imaging Sci [serial online] 2012 [cited 2018 Mar 21];2:27. Available from:

   Introduction Top

Fahr's disease is a rare disorder that was first described by Karl Theodor Fahr in 1930. [1] It usually presents with either slow progressive cognitive decline, psychiatric disturbance, or movement disorders. The radiological study shows it is bilateral with extensive calcification in the subcortical structures. [1]

Recent evidence links Fahr's disease to epilepsy as its acute presentation. [2] However, the etiology and pathophysiology of such association has yet to be elucidated. Another mode of acute presentation may be syncope.

We describe a patient with an acute deterioration in the level of consciousness and a CT scan demonstrating both subarachnoid blood and idiopathic basal ganglia calcification (IBGC). Further investigations showed a right posterior communicating artery aneurysm to be the source of the hemorrhage. We postulate that the extensive calcification in Fahr's disease negatively affects both brain parenchyma and intracranial vessels predisposing these individuals to such an acute presentation.

   Case Report Top

A 54-year-old housewife without any significant previous medical history, or any neurological problem presented with a transient loss of consciousness followed by headache and confusion. She had no history of movement or cognitive disorder prior to this event. No family history of subarachnoid hemorrhage or cognitive disability was obtained. On presentation her vital signs were stable and her blood pressure normal. She was drowsy and displayed signs of meningeal irritation. Her obtunded state was transient as she improved rapidly and soon became fully oriented. Her blood investigation, which included coagulation profile, blood cell count and serum electrolytes, was normal. Brain computerized tomography (CT) showed two major findings: first, diffuse bilateral subarachnoid hemorrhage involving the basal cisterns and both Sylvian fissures; and second, extensive calcification involving the basal ganglia, thalamus, corona radiata, and deep cerebellar nuclei [Figure 1].
Figure 1: Axial noncontrast CT scan of the brain shows extensive symmetrical calcification at the level of the (a) cerebellum, (b) basal ganglia, (yellow arrow) (c) thalamus and (d) White matter.

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Formal cerebral angiography revealed a right posterior communicating artery aneurysm as the probable source of the SAH. It measured 7.8 x 5.7 x 4.2 mm with a neck of 3.3 mm. An attempt at coiling this aneurysm failed because of a tortuous internal carotid artery precluding safe access to the aneurysm [Figure 2].
Figure 2: Right internal carotid angiogram showing a multilobulated right posterior communicating artery aneurysm measuring 7.8 x 5.7 x 4.2 mm with the neck of the aneurysm measuring 3.3 mm (white arrow).

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The patient was thereafter taken to the operating room where she underwent a right pterional craniotomy and clipping of the posterior communicating artery aneurysm. Her postoperative course was complicated by a right-sided upper extremity monoparesis due to a small middle cerebral artery territory ischemic infarct. However, over the following days she improved but experienced mild vasospasm that was treated medically with Euvolemia and Milrinone. She was also investigated for disorders that may cause abnormal calcium deposition which proved negative. Her serum calcium, phosphorus, and alkaline phosphatase were normal. The patient was eventually discharged from the hospital to a rehabilitation program where she showed significant improvement. The 6-month follow-up angiogram revealed no new aneurysms and no recanalization of the clipped aneurysm.

   Discussion Top

Fahr's disease, or idiopathic basal ganglia calcification is a rare syndrome that is characterized by abnormal intracranial calcification in the absence of any systemic calcium disorder. Different names have been given to abnormally excessive calcification within the brain parenchyma and cerebral vessels, reflecting the confusion regarding what causes this disorder [Table 1]. [1]
Table 1: Names of IBCG with vascular predilections

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Calcification has been described in the globus pallidus, caudate nucleus, putamen, thalamus, dentate nuclei, cerebellar lenticular nucleus, thalamus, the white matter of the cerebral cortex, as well as major intracranial vessels and those supplying the basal ganglia and the cerebellum. [3]

Affected individuals may remain asymptomatic. Typical presentation starts in the 4th to 5th decade of life with a slow cognitive decline, psychiatric abnormalities or movement disorders such as Parkinson's tremor, dystonia or cerebellar ataxia. [4]

Microscopic and biochemical analysis of brain deposits in Fahr's disease reveals that the stroma contains mainly calcium and protein without collagen or mucopolysaccharides. These deposits occur in vessel walls of arterioles, capillaries, veins, and in the perivascular spaces. [5] The calcium deposits are generally symmetrical and may be seen in the walls of small and medium sized vessels that could have resulted from inflammatory processes in the vessels. [6]

An acute deterioration in the level of consciousness may be the first symptom of Fahr's disease. A potential cause may be a complex-partial seizure as reported in a patient who had had a mild psychiatric disturbanceprior to a seizure episode. [7] In another case, Simone et al., described a 69- year-old patient who presented with recurrent episodes of deterioration in the level of consciousness and who was found to have classical radiological findings of Fahr's disease, in addition to pseudo-hypoparathyroidism, the correction of which improved his clinical status. [8]

Subarachnoid hemorrhage from a ruptured intracranial aneurysm has a poor prognosis with mortality rate of 50%, with 20% of survivors remaining severely disabled. [9] Histopathologically, aneurysms are associated with a loss of the media interna along with the elastic lamina as well as a thinning of the wall. There is also an associated intimal thickening in the parent artery. In larger aneurysms calcification may be seen either in the wall of the vessels or at the neck of the aneurysm. [10]

Earlier descriptions of Fahr's disease postulate a vascular pathophysiological process with calcification in both small and large vessels. Our case represents IBGC presenting with an SAH as a first presentation. Despite the heavy calcification seen on imaging she was asymptomatic before the event. We suggest that this could represent a subset of patients in whom there may be a predilection for intracerebral vessel symptomatology prior to the eventual onset of cognitive and psychiatric disturbances. The association of IBGC and an intracranial aneurysm has to date remained unreported in the literature. This case represents a first for Fahr's disease presenting with an aneurysmal subarachnoid bleeding.

   Conclusions Top

Fahr's disease is a chronic slowly progressive neurodegenerative disorder that most commonly will present with acute deterioration in the level of consciousness, secondary to seizures. We report a case of Fahr's disease in which this acute deterioration was secondary to an aneurysmal subarachnoid hemorrhage.

This observation suggests that a brain CTA should be performed in patients with unexplained recurrent episodes of loss of consciousness, to rule out an aneurysm, even if they are known to have IBGC, so as to not attribute it to an epilepsy disorder.

   References Top

1.Manyam BV. What is and what is not 'Fahr's disease'. Parkinsonism Relat Disord 2005;11:73-80.  Back to cited text no. 1
2.Hoque MA, Siddiqui MR, Arafat Y, Khan SU, Rahman KM, Mondol BA, et al. Fahr's disease: A very rare cause of epilepsy. Mymensingh Med J 2010;19:127-9.  Back to cited text no. 2
3.Victor M RA. Calcification of vessels in basal ganglia and cerebellum (hypoparathyroidism and Fahr syndrome), in Principles of neurology. RA Victor M, editor. New York: McGraw-Hill; 2001. p. 1032-3.  Back to cited text no. 3
4.Wszolek ZK, Baba Y, Mackenzie IR, Uitti RJ, Strongosky AJ, Broderick DF, et al. Autosomal dominant dystonia-plus with cerebral calcifications. Neurology 2006;67:620-5.  Back to cited text no. 4
5.Chalkias SM, Magnaldi S, Cova MA, Longo R, Pozzi-Mucelli RS. Fahr disease: Signifi cance and predictive value of CT and MR fi ndings. Eur Radiol 1992;2:570-5.  Back to cited text no. 5
6.Elshimali YI. The value of differential diagnosis of Fahr's disease by radiology. Internet J Radiol 2005;4:1. Available from: [Last accessed on 2012 Feb 20].  Back to cited text no. 6
7.Sentimentale A, Matteoli M, Giovannelli M, De Dominicis C, Corsino M, Ferri E, et al. Fahr's disease detected on a head CT scan in patient with "epileptic syncope" in the Emergency Department. Intern Emerg Med 2010;5:263-5.  Back to cited text no. 7
8.Simone O, Tortorella C, Antonaci G, Antonaci S. An unusual case of transient loss of consciousness: The Fahr's syndrome. Recenti Prog Med 2008;99:93-6.  Back to cited text no. 8
9.Hop JW, Rinkel GJ, Algra A, van Gijn J. Case-fatality rates and functional outcome after subarachnoid hemorrhage: A systematic review. Stroke 1997;28:660-4.  Back to cited text no. 9
10.Stehbens WE. Histopathology of cerebral aneurysms. Arch Neurol 1963;8:272-85.  Back to cited text no. 10

   Authors Top

Hosam Al-Jehani


  [Figure 1], [Figure 2]

  [Table 1]

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