Neurosurg.Rev. 19111996)119-121 Clinical and radiological evaluation of angiographically occult, calcified intracranial vascular malformation. Case report Siileyman Baykal ~, Sava~ Ceylan 1, Hasan Din~ 2, Kayhan Kuzeyli 1, Eray Soylev 1, Haydar UsuP, and Fadil Aktiirk ~ Departments of ~Neurosurgery and 2Radiology, K T U Medical Faculty, Trabzon, Turkey Abstract In this study, we present an angiographically occult, calcified intracranial vascular malformation. This lesion is rare and has some therapeutic difficulties and different approaches by authors. In this article, we also discuss the clirfical, radiological characteristic features of this lesion. We pay attention on the totally calcified malformation. Keywords: Angiography, calcification, magnetic resonance imaging. history of complex partial seuzures insufficiently controlled by antiepileptic drugs. The physical and neurological examination on admission was normal. Plain films show an irregular calcification in the left middle fossa (Figure 1). M R I show a serpentine lesion in the left temporal lobe with mixed isointens region on T2-weighted images (Figure 2a, b). The angiogram was without shunting, blush, or abnormal vessels (Figure 3a, b). The MR-angio was also normal (Figure 4). The diagnosis was totally calcified vascular malformation. 1 Introduction The term "angiographically occult intracranial vascular malformation" (OVM) is applied to a group of intracranial vascular malformations (arteriovenous, cavernous, venous angiomas or capillary telangiectases) [1, 2, 3, 4, 7, 8, 12, 16, 17]. In the literature, the term thrombosed malformations and occult intracranial vascular malformations have been used interchangeably [7]. Magnetic resonance imaging of these patients can often help to suggest the diagnosis of angiographically occult vascular malformations with increased confidence [10, 11, 14, 15]. In this report, we present a patient with radiologieally verified angiographically occult, calcified vascular malformation and discuss her clinical and magnetic resonance imaging (MRI) characteristics. 2 Case report A 22-year-old woman presented with a 16-year 9 1996by Walterde Gruyter& Co. Berlin.NewYork Figure 1. Lateral plain skull film showing a huge calcification in the suprasellar region. Note an irregular and heterogen appearance, 120 Baykal et al., Clinicaland radiologicalevaluation of OVM Figure 2. T2-weighted axial (a) and coronal (b) MR images, showing an irregular hypointens lesion located in the left temporal lobe, The patient and her family did not admit surgical exploration. Her seizures were controlled by carpamazepine and valproic acid and discharged. 3 Discussion Because of common radiographic findings and a spectrum of common histopathological findings, thrombosed arteriovenous malformations and occult vascular malformations seem to have similar presentations and prognosis and indeed may represent the same disease entity [7, 10, 12]. The responsible mechanisms for the partial or complete thrombosis of angiographicallyoccult intracranial vascular malformations are arteriosclerosis, embolism, hem- orrhage with secondary vascular compression, slow blood flow, intravascular turbulency due to the tortuosity of the vessels, and hypercoagulability [12,13]. LOBATOet al. reported some calcification in approximately 10% of patients with OVM's on skull x-ray films [1, 9, 12]. They also demonstrated calcification in 24% of patients on the nonenhanced CT scan [12]. Two cases of dystrophic intracranial calcification due to arteriovenous malformations were reported by Yu et al. They explained the probable pathogenetic mechanism for calcification as a result of "cerebral steal" by the arteriovenous malformation [18]. We are not certain whether calcification in our case is explained by the proposed mechanism in our case, In this lesion, OVM was calcified. This huge Figure 3. Normal angiogramswere shownon the anteroposterior (a) and lateral (b) projection. Figure 4. MR-angiogramwas normal. Neurosurg. Rev. 19 (1996) Baykal et al., Clinical and radiological evaluation of OVM 121 calcification is shown by plain x-ray a n d MRI. In the literature review, a similar lesion was not d e m o n strated. and M R I findings may differentiate these two lesions. H e a d a c h e and seizure disorders are the most comm o n clinical presentation of OVM's [5, 6, 15]. In addkion, episodic progressive worsening is the second most clinical p r e s e n t a t i o n [15]. These clinical presentations may suggest the presence of a low grade n e o p l a s m but, the duration of the patient's seizures It was postulated that CT scan a n d M R I a p p e a r to be a b o u t equally sensitive in the detection of these lesions, a l t h o u g h the M R I is p r o b a b l y slightly more specific [14, 15]. B u t if calcification is present, C T scan is superior to M R I for the evaluation of calcified lesion. A n g i o g r a p h y is essential for its vascular nature of this lesion. References [1] BECKER DH, JJ TOWNSEND,RA KRAMER: Occult cerebrovascular malformations. A series of 18 histologically verified cases with negative angiography. Brain 102 (1979) 249-287. [2] BELLBA, BE KENDALL,L SYMON:Angiographically occult arteriovenous malformations of the brain. J Neurol Neurosurg Psychiatry 41 (1978) 1057-1064 [3] B1TOH S, H HASEGAWA,M FUJIWARA:Angiographically occult vascular malformations causing intracranial hemorrhage. 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J Neurosurg 69 (1988) 350-355 [16] TOMLINSONFH, OW HOUSER, BW SCHEITHAUER,H OKAZAKI,TM SUNDT, JE PARISI: Angiographically occult vascular malformations: A correlative study of features on magnetic resonance imaging and histological examination. Neurosurgery 34 (1994) 792-800. [17] WAKAIS, Y UEDA, S INOH: Angiographically occult angiomas: a report of thirteen cases with an analysis of the cases documented in the literature. Neurosurgery 17 (1985) 549-556. [18] Yu YL, EK Cniu, E Woo, FL CHAN,WK LM, CY HUANG, PW LEE: Dystrophic intracranial calcification: CT evidence of "cerebral steal" from arteriovenous malformation. Neuroradiology 29 (6) (1987) 519-22 Submitted July 24, 1994. Revised February 10, 1995. Accepted February 14, 1995. Dr. Siileyman Baykal KTfJ Tip Fak01tesi N6rosirtirji Klinigi 61080 Trabzon Turkey