Case record...Occipital lobe cavernoma

CASE OF THE WEEK
PROFESSOR YASSER METWALLY
CLINICAL PICTURE

CLINICAL PICTURE:

A 30 years old male patient presented clinically with a history of grand mal fits that are occasionally preceded by
vivid visual hallucinations.

RADIOLOGICAL FINDINGS

RADIOLOGICAL FINDINGS:

Figure 1. Type II left occipital cavernoma. Precontrast MRI T1 images. The characteristic MR imaging appearance
of cavernomas is a well-defined, lobulated lesion with a reticulated core of heterogenous signal intensity on both T1
and T2 weighted sequences resulting from thrombosis, fibrosis, calcification, and hemorrhage. Extracellular and
intracellular methemoglobin and thrombosis are responsible for the high intensity signal within the lesion, while
calcifications, fibrosis, and acute and subacute blood are responsible for the low signal areas. The cavernoma in the
current case has the classic quot;popcornquot; appearance characteristic of type II cavernomas.



Conclusion

MRI picture of occipital cavernoma.

The MRI mixed signal intensity of the precontrast MRI T1 images and the MRI T2 images is due to the presence of
altered blood of different ages.

1. The MRI T1 precontrast hyperintensity is due to methemoglobin

2. The MRI T2 hypointensity is due to hemosiderin pigments.

Table 1. Evolution of MR imaging signal characteristics [56]

Iron
Iron-containing Red cell
Phase Time oxidation T1 T2 T2*
molecule membranes
state
Hyperacute Hours Oxyhemoglobin Fe2+ Intact Hypointense Hyperintense
Acute Hours to Deoxyhemoglobin Fe2+ Intact iso/
Hypointense Hypointense
days Hypointense
Early Days to 1 Methemoglobin Fe2+ Intact
Hyperintense Hypointense
subacute week
Late 1 week to Methemoglobin Fe2+ Degraded
Hyperintense Hyperintense
subacute months
Chronic >months Hemosiderin Fe2+ Degraded iso/
Hypointense Hypointense
Hypointense
Abbreviations: Fe, iron; iso, isointense relative to normal brain.

Table 2. Cavernomas types [56]

Type Neuroimaging characteristics
Type I Is a subacute bleed dominated by methemoglobin and therefore homogeneously hyperintense on TI
weighted images (Fig. 10)
Type II The lesions have the classic quot;popcornquot; appearance, heterogeneous on both TI and T2 weighted sequences
(Fig. 4, the current case)
Type III The lesions are isointense to hypointense on both TI and T2 weighted images because of the predominance
of chronic blood products (Fig. 11)
Type IV The lesions are tiny, punctate, foci hypointense on both TI and T2 weighted sequences. These type IV
lesions are often multiple and best seen on gradient echo sequences (Fig. 8). In contrast with
telangiectasias, type IV lesions rarely enhance

DIAGNOSIS:

DIAGNOSIS: INTRAMEDULLARY CAVERNOMA

DISCUSSION

DISCUSSION:

Cavernous malformations (CMs) are one of the four major types of vascular malformations of the central nervous
system as classified by McConnick [1]. These lesions are composed of well-circumscribed sinusoidal vascular
channels containing blood in various stages of evolution [1 -5]. In the literature, there are a number of synonyms for
CMs including cavernomas, cavernous angiomas, angiographically occult vascular malformations, and cavernous
hemangiomas [2-15]. In contrast with arteriovenous malformations and developmental venous anomalies, Cavernous
malformations have immature blood-vessel wall components, lacking elastin and a significant amount of smooth
muscle cells. Originally thought to he rare, CMs are now more commonly discovered because of improvements in
neuroimaging techniques. On MR imaging, they are seen as well- circumscribed, reticulated, mixed signal-intensity
lesions because of the mixture of oxyhemoglobin, deoxyhemoglobin, extracellular methemoglobin, and intracellular
methemoglobin surrounded by an area of hypointensity that corresponds to hemosiderin deposition [6-16] . [Fig. 4]

Clinically, patients with cavernous malformations are often symptomatic at some point in their lives [7-11,13,17-22].
A significant number of patients are left with neurologic deficits. The recommendations for treatment have varied
widely and have ran the entire gamut from operating on the lesions as soon as they are discovered to watchful
waiting despite recurrent bleeds. The recommendations for treatment should be based on the existing knowledge of
the natural history of the disease.

 Patient demographics, lesion location, and presentation

Cavernous malformations affect 0.4-0.9% of the general population according to large autopsy studies [1,13,23].
They constitute 5-16% of all vascular malformations [18,20,24,25]. Most of the lesions are found in the supratentorial
compartment (80- 92%), whereas 8-20% are infratentorial [7,18,19,22]. In a study from the University of Toronto
Vascular Malformation Study Group in 1997, Porter et al [19] classified lesions into deep and superficial, theorizing
that the natural history of lesions in these two locations were significantly different. Deep lesions were those located
in the brainstem, cerebellar nuclei, basal ganglia, and the thalamus. Based on this grouping and using a database of
353 patients, approximately 60% of lesions are superficial, 30% are deep, and 3% are within the spinal cord. In
terms of specific locations, CMs follow the volume distribution of the neuraxis [7], being most common in the frontal
lobe (28%) and followed by the temporal lobe (15.2%). Seventeen to fifty-four percent of patients have multiple
lesions [9,19,22,26]. Fifty to eighty- five percent of patients with multiple CMs have a familial type of lesion
[9,11,18,22,26,27].

Figure 4. Cavernous malformation (CM): classic morphology. (A) T I weighted MR imaging shows an intra-axial
heterogeneous mass (arrow) with pockets of high signal intensity. (B) T2 weighted MR imaging shows a
heterogeneous mass (arrow) with a complete rim of hypointensity (hemosiderin) and loculated areas of high signal
intensity.

Cavernous malformations appear to have no significant sex predilection. The usual range of age at presentation is
from the 2nd to the 5th decades, with the mean usually in the latter 4th decade [ 17,19]. The most common
presentation in most series is seizures [7,8,11-13,18]. Seizures were the most common presentation (36%) in the series
by Porter et al [19]. The second most common presentation was hemorrhage (25%). Twenty percent presented with
focal neurologic deficits without radiographic hemorrhage; 12% were found incidentally; and 6% presented with
headaches. In a review of patients with intraventricular CMs (45 cases), Reyns et al [10] found that the common
clinical presentations were similar to tumors in the same location (ie, hypothalamic dysfunction, increased
intracranial pressure, hydrocephalus). Twenty percent had intraventricular hemorrhage and 16% presented with
seizures [10]. In a review of four patients with third ventricular CMs, Sinson et al noted that none of the patients
presented with seizures. Their patients presented with hydrocephalus, memory loss, and hypothalamic dysfunction
[15].

Figure 5. Radiation induced cavernoma in a patient treated from medulloblastoma with surgery and radiation. A,B
immediately following treatment, C,D a year after, and E,F one year later, notice the progressive development of a
pontine cavernoma.

The clinical manifestations of supratentorial
cavernomas in one study. 55

Age of first haemorrhage in 47 cases of
supratentorial cavernomas in one study. 55

DE NOVO FORMATION AND FAMILIAL CAVERNOUS MALFORMATIONS

Initially, all cavernous malformations were thought to be congenital. There is now evidence that CMs can arise de
novo. Factors associated with de novo formation of CMs are previous irradiation [6,9,21,28,29], genetics in familial
cases [22,27], viruses [21], hormonal influences especially in pregnancy [21], and local seeding along a biopsy tract
[6,30]. There is a report of a lesion arising de novo in a patient with neither previous irradiation nor a family history
[28]. This patient underwent excision of an acoustic neuroma and was subsequently found to have a CM on follow-up
imaging.

Cavernous malformations have been shown to arise in patients with previous irradiation (Fig. 5). Studies involving
children treated with radiotherapy showed that a quot;second hitquot; by irradiation to genetically predisposed tissue may
lead to the formation of CMs [6,29,31]. Some authors believe that CMs related to irradiation are more prone to
hemorrhage [29]. Once these new lesions are formed, the late radiation effects may lead to growth by mechanisms of
angiogenesis, hemorrhage, and thrombosis [9,29].

Familial cases of CMs have been shown to have a 0.2-0.4% incidence per patient per year of de novo lesion formation
[22,27,31]. In a recent prospective study involving 33 patients belonging to unrelated French families, 30% of
patients were noted to develop new lesions during a two-year follow-up period [32]. The familial type is inherited by
autosomal dominant transmission with incomplete penetrance [33]. In Hispanic Americans, the genetic defect
responsible for familial lesions, CCM 1, has been localized to chromosome 7q ll-22 [8,22]. Further analysis revealed
that KRIT I (a gene at the 7ql 1 -22) mutations are responsible for cerebral CMs [34]. In non-Hispanic Caucasians,
two gene loci were identified to be responsible for cerebral CMs: CCM 2 at 7pl3-15 and CCM 3 at 3q25.2-27 [33].
Aside from having a higher rate of de novo formation as compared with sporadic lesions, some authors believe that
familial lesions have a higher annual hemorrhage rate [27,32].

Developmental venous anomalies (DVAS) have also been reported to be associated with and possibly play an etiologic
role in the formation of CMs [21,23,31,35]. DVAs (previously referred to as venous angiomas) are the most common
cerebral vascular malformations, with approximately 4% of the population being affected [36,37]. DVAs simply
represent an extreme variant of the normal venous drainage, however. DVAs drain normal brain and must be
preserved when CMs are excised [38]. They typically appear on MR imaging as radiating, linear flow-voids (a quot;caput
medusaquot; pattern) centered on a large collecting vein (Fig. 6). DVAs typically enhance with contrast. According to
Dillon et al [39], most DVAs have a collector vein stenosis, and this venous restrictive disease leads to an increased
pressure within the capillary bed. This increased venous pressure may cause niicrohemorrhages or red blood cell
diapedesis within the parenchyma that in turn leads to angiogenic proliferation. The presence of red blood cells
activates a vicious cycle wherein the extruded blood draws fibroblasts that lay down fragile, leaky vessels which in
turn leads to more microscopic or gross hemorrhage. Endothelial development in chronic hematomas supports this
mode of de novo CM development [35]. In relation to this, a study by Sure et al using immunohistochemical
techniques with proliferating cell nuclear antigen (PCNA) and vascular endothelial growth factor (VEGF) showed
that CMs have the capacity for endothelial proliferation and neoangiogenesis [40]. A higher concentration of these
angiogenic factors in CMs may also explain the development of new cavernous malformations along a biopsy tract. It
may be that a small amount of CM tissue transplanted to any point along the biopsy tract may induce the
transformation of normal capillaries or the growth of new, fragile vessels. Another explanation is that the

transplanted CM tissue may become recanalized by nearby parenchymal vessels [30].

HISTOPATHOLOGY

Cavernous malformations are discrete, well-circumscribed lesions composed of thin-walled, dilated vascular channels
lined by a single layer of endothelium in a collagenous, fibronectin-rich matrix [7- 9,11,17,33,40,41] (Fig. 7). This
conglomeration of sinusoidal vascular channels and its matrix is devoid of elastin, laminin , subendothelial smooth
muscle cells, and other mature vascular wall components [9,42]. The surrounding parenchyma contains hemosiderin-
laden macrophages and iron-laden glial cells [11]. The lack of intervening brain parenchyma is one of the hallmarks.
CMs, however, are not always compact. They may at times be racemose, containing small satellite-like projections
into the surrounding brain [9,43]. Grossly, lesions have often been described as mulberry-like in appearance because
of the berry-like clusters that contain hemorrhage in various stages of organization [44]. Ultrastructurally,
endothelial cells are seen to line the thin cavernous walls that are made up of amorphous, disorganized collagen.
Tight junctions and pericytes are noted to be less in number as compared with those in normal blood vessels [41].
The combination of thin walls, composed of amorphous material lacking subendothelial support, and the small
number of tight junctions and pericytes predispose to the known propensity of these lesions to leak or bleed [41].
immunohistochemical studies have shown that these lesions do not express laminin, signifying immature and brittle
vessels [9]. They stain significantly for fibronectin, consistent with proliferating and leaky vessels [9].

Table 3. Pathological characteristics of cavernomas that differentiate them from arteriovenous malformation

 Cavernous angiomas (cavernomas) consist of enlarged capillaries with the following characteristics:

 Sinusoidal

 Single layer of endothelium

 Thin collagenous wall

 Lack of smooth muscle fibers and elastic fibers

 Capillaries are immediately adjacent to each other, with no intervening neural tissue.

 The surrounding parenchyma contains hemosiderin-laden macrophages and iron-laden glial cells.

 They typically are not associated with enlarged feeding arteries or draining veins, and blood flow is low or
even stagnated (cavernomas are angiographically occult).

 Grossly, they may range from soft to hard.

 Thrombosis, calcification, or ossification results in a harder lesion.

 Adjacent neural tissue may be affected, and small hemorrhages result in hemosiderin staining (iron salts may
incite an epileptogenic focus). Tissues also may be gliotic.

Figure 6. Cavernous malformation and associated developmental venous anomaly (DVA). (A)'I'2 weighted MR
imaging shows a heterogeneous mass with a hemosiderin ring (arrow). (B) Gadolinium-enhanced Tl weighted MR
imaging shows a radiating collection of vessels adjacent to the CM that join one large collecting vein (arrow).

Figure 7a. Histopathology. (A) Microscopic section (trichrome stain) shows a mass of closely apposed vessels of
varying size. The vessel walls have a variable thickness, and there is no intervening brain. (B) Whole mount
(trichrome stain) of a CM of the third ventricle shows a plexus of vessels with some intervening brain at the
periphery.

Figure 7b. Example of cavernomas, notice absence of feeding arteries or draining veins

Figure 7c. Pontine cavernoma, notice absence of feeding
arteries or draining veins

Figure 7d. For comparison, an arteriovenous malformation, notice the feeding arteries and the draining veins

IMAGING

Radiographically, high resolution MR imaging is the diagnostic tool of choice for detecting and identifying CMs. On
noncontrast CT, CMs frequently appear as focal areas of increased density within the brain often without mass effect
(Fig. 8). The increased density either represents calcium, blood, or a combination of the two. The margins of the
lesion are usually indistinct and the increased density may have a stippled appearance. The differential diagnosis on
CT includes low-grade calcified neoplasms, hemorrhage, and vascular malformations. MR imaging is required to
make a more definitive diagnosis. The characteristic MR imaging appearance is a well-defined, lobulated lesion with
a reticulated core of heterogenous signal intensity on both T1 and T2 weighted sequences resulting from thrombosis,
fibrosis, calcification, and hemorrhage. Extracellular and intracellular methemoglobin and thrombosis are
responsible for the high intensity signal within the lesion, while calcifications, fibrosis, and acute and subacute blood
are responsible for the low signal areas. On T2 weighted or gradient echo images, there is a peripheral ring of
hypointensity that corresponds to the deposition of hemosiderin and iron in the surrounding brain parenchyma [7-
11,14,16,19,22]. The hemosiderin ring may not be evident in intraventricular cavernous malformations.
Intraventricular CMs can exhibit rapid growth and be quite voluminous, leading to a diagnosis of a tumor instead of
a vascular malformation [10,21] (Fig. 9).

Table 4. Neuroimaging characteristics of cavernomas

 On noncontrast CT, CMs frequently appear as focal areas of increased density within the brain often without mass
effect. The increased density either represents calcium, blood, or a combination of the two. The margins of the lesion
are usually indistinct and the increased density may have a stippled appearance.

 The characteristic MR imaging appearance is a well-defined, lobulated lesion with a reticulated core of heterogenous
signal intensity on both T1 and T2 weighted sequences resulting from thrombosis, fibrosis, calcification, and
hemorrhage. Extracellular and intracellular methemoglobin and thrombosis are responsible for the high intensity
signal within the lesion, while calcifications, fibrosis, and acute and subacute blood are responsible for the low signal
areas.

 On T2 weighted or gradient echo images, there is a peripheral ring of hypointensity that corresponds to the deposition
of hemosiderin and iron in the surrounding brain parenchyma

Cavernous malformations are angiographically occult lesions. They are by far the most common type of
angiographically occult vascular malformation [13,43]. Earlier reports on angiography in CMs described venous
pooling or a capillary blush in some lesions [9,11]. Presently, angiography has no role in the diagnosis. CT scan is a
relatively sensitive test to detect cavernous malformations, but it is not specific. Vaquero stated that in their series,
CT scanning was only able to diagnose CMs in 44% of patients [45]. Marraire et al in a later study reiterated the
high sensitivity (70-100%) and low specificity ({50%) of this modality in the diagnosis of CMs [9]. On CT the
presence of thrombosis and hemorrhage in various stages of evolution cannot be accurately characterized.

Zabramski et al classified CMs into four types (I- IV) based on the MR imaging appearance [22]. Type I is a subacute
bleed dominated by methemoglobin and therefore homogeneously hyperintense on TI weighted images (Fig. 10).
Type II lesions have the classic quot;popcornquot; appearance, heterogeneous on both TI and T2 weighted sequences (Fig. 4).
Type III lesions are isointense to hypointense on both TI and T2 weighted images because of the predominance of
chronic blood products (Fig. 11). Type IV lesions are tiny, punctate, foci hypointense on both TI and T2 weighted
sequences. These type IV lesions are often multiple and best seen on gradient echo sequences [11,22,46] (Fig. 8). In
contrast with telangiectasias, type IV lesions rarely enhance [6]. Gradient echo sequences best identify these lesions
because of the susceptibility artifact from microscopic deposits of hemosiderin [6]. Several authors have noted that
patients with type I and type 11 lesions were more commonly symptomatic compared with the other types
[22,27,32].Willinsky et al [16] in 1996 reviewed their own series (156 patients) and on serial MR imaging studies
found no significant correlation between the type of CM (according to Zabramski's classification) and the natural
history of the lesion. None of the four morphological appearances were immune from change, and the evolution of the
lesions was not predictable based on the original morphology (Fig. 12).

Table 2. Cavernomas types

Type Neuroimaging characteristics
Type I Is a subacute bleed dominated by methemoglobin and therefore homogeneously hyperintense on TI
weighted images (Fig. 10)
Type II The lesions have the classic quot;popcornquot; appearance, heterogeneous on both TI and T2 weighted sequences
(Fig. 4, the current case)
Type III The lesions are isointense to hypointense on both TI and T2 weighted images because of the predominance
of chronic blood products (Fig. 11)
Type IV The lesions are tiny, punctate, foci hypointense on both TI and T2 weighted sequences. These type IV
lesions are often multiple and best seen on gradient echo sequences (Fig. 8). In contrast with
telangiectasias, type IV lesions rarely enhance

Figure 8. Multiple CMs. (A) Noncontrast CT shows two
areas of hyperdensity with no mass effect and no edema.
(B,C) T2 weighted MR imaging shows two left frontal
lobe lesions. Both have central areas of mixed signal
intensity and a surrounding rim of hemosiderin. (D)
Gradient echo MR imaging shows multiple foci of
hypointensity. Only the largest lesions were evident on
the spin-echo images. The small foci that are seen only
with the gradient echo technique have been referred to as
type TV CMs.

Figure 9. Intraventricular CM. (A) Sagittal TI weighted MR imaging shows a heterogeneous hyperintense lesion in
the third ventricle (arrow). (B) Axial T2 weighted MR imaging shows a hemosiderin rim surrounding the
hyperintense lesion (arrow).

In cases where a CM is suspected but the radiologic image is not pathognomonic, serial imaging is of value if
immediate surgical intervention is not warranted. Differential diagnoses include neoplasms, infectious and
inflammatory masses, hemorrhagic emboli, and hematomas. If there is a recent bleed or thrombosis in a CM, the
typical features of a CM are not evident (Figs. I0 and 11). The hemosiderin ring may be obscured by a recent bleed
and therefore follow-up MR imaging is important to establish CM as the cause for the bleed. Peri-lesional and
extralesional hemorrhage may be evident outside the hemosiderin ring [16]. Repeat MR imaging is also needed in
patients who report a worsening of symptoms or when new deficits are detected by the clinician. The presence of
edema and mass effect on MR imaging may correlate with new signs and symptoms that the patient has developed
[16] (Figs. 10-12). Hemorrhage outside the hemosiderin ring may be evident in patients with new clinical findings or
worsening of an existing deficit [16]. A fluid/fluid level may be evident in some active CMs (Fig. 14). On serial MR
imaging, a change in the signal intensity within the lesion may or may not correspond with recent clinical events.
Clinical deterioration can, however, also occur without any significant change in the MR imaging [19]. On MR
imaging, there may be changes in the size of the CM or the signal intensity within the lesion without a corresponding
clinical event in the patient.

Figure 10. Type I CM. (A) TI weighted MR imaging shows a homogeneous hyperintense lesion. (B) T2 weighted MR
Imaging shows a lesion with a well-defined hemosiderin rim and no surrounding edema.

Figure 11. Type 3 CM. (A,B) Tl and T2 weighted MR imaging shows a homogeneous hypointense lesion on both
sequences (arrows).

There are pitfalls in the interpretation of postoperative MR imaging of CM. The postoperative MR imaging often
appears similar to the preoperative image. This occurs despite the impression at surgery that there was a complete
resection. The most plausible explanation for this is that the excision cavity is filled with organizing blood products.
The natural history of such postoperative findings is unknown, so ongoing serial imaging and clinical follow-up is
prudent.

NATURAL HISTORY

There has been much controversy regarding the natural history of CMs. Several factors have lead to this confusion:
the variability of the periods at risk identified by different authors, different definitions of hemorrhage, patterns of
referral, MR imaging versus clinical/radiographic studies, and the timing of the MR imaging follow-up. Because
CMs were originally considered to be congenital, early reports defined the period at risk as beginning from birth.
These studies assumed that the CMs were present at birth and the risk of bleeding was the same throughout life [7].
These retrospective studies had lower hemorrhage rates compared with studies that based their calculations on the
time from the initial diagnosis to the final follow-up. The evidence is clear that CMs can be acquired [6,9,22,27-
29,32,35,40].

In the literature, the definition of hemorrhage in relation to CMs has varied. This inconsistency has lead to
significant variation in the estimated hemorrhage rate. It is better to use a radiologic definition of hemorrhage to
eliminate any ambiguity quot;acute or subacute blood located outside the hemosiderin ring or an increase in lesion size
by 20% or more in diameter on serial imaging with associated mass effect and/or edemaquot; (Fig. 15) [16]. Because of
the observation that several patients being followed had clinical deterioration without radiologic evidence of
hemorrhage, as defined above, Porter et al used the term clinical/neurologic events to study the natural history of
CMs. A clinical/neurologic event was defined as deterioration in symptoms as noted by the patient and worsening or
new onset of neurologic signs as detected by the clinician [19]. New symptoms alone (eg, increased headache only)
were not sufficient to qualify. Clinical/neurologic events are independent of hemorrhages and therefore may or may
not be accompanied by radiologic proof of hemorrhage (Fig. 14) [19]. As symptoms and deficits are more important
to the patient than results of MR imaging, it is preferable to report event rates, as these are more encompassing in
terms of clinical deterioration (with or without hemorrhage) as opposed to hemorrhage rates that may or may not
have clinical significance.

Figure 12. Morphological changes on serial imaging in a patient with CMs. (A) Initially the proton density weighted
MR imaging shows that the occipital pole lesion is hyperintense (arrow). (B) Later, it has a heterogeneous
appearance (arrow). (C) Finally, it is homogeneously hypointense (arrow).

In defining the natural history of CMs, it would be beneficial if patient or lesional factors could be identified that
predict a poor prognosis. Throughout the years, several authors have reported on patient and lesional characteristics
that may predict the natural history of these lesions. Lesion presentation, location, size, number, MR imaging
appearance, presence of DVAS, familial occurrence, timing from initial event, and patient age, sex, and pregnancy
have all been studied [6-9,12-17,19,21-23,26,27,32, 42,43,47-49].

Figure 13. Symptomatic hemorrhage in a cerebellar cavernoma (confirmed surgically)

The most significant predictor of clinical events is lesion location [19]. When lesions were classified as supratentorial
versus infratentorial, the infratentorial lesions had a higher event rate (10.61/o/year vs. 0.41/o/year). In a recent
review of the same database with a longer follow-up and more patients, there was still a statistically significant
difference in the annual event rates between these two locations (6.5% for infratentorial vs. 0.7% supratentorial)
(Peter Rivera, MD, University of Toronto Vascular Malformation Study Group, February 2002). The significance of
location assumes an even stronger power when the lesion location is classified as superficial versus deep. The annual
event rate reported by Porter et al is 10.6% for the deep lesions and 0% for the superficial lesions. A more recent
study shows the same trend, with deep lesions having a statistically significant difference in annual event rates when
compared with superficial lesions [19]. When a Cox proportional hazards modeling was used to verify the relative
importance of these various factors, lesion location when classified as deep versus superficial was the most important
predictor of subsequent events. There are several hypotheses as to why deep CMs have more clinical events than
superficial CMs. Intuitively, the most plausible explanation is that the eloquence of deep structures will lead to
clinical signs and symptoms even with a small change in the lesion., either growth or hemorrhage. The same small
change would probably not manifest any signs in a superficial lesion. There may also be an inherent physiologic and
structural difference between superficial and deep structures that may predispose to lesion activity. Differences in
venous pressures between deep and superficial neural tissue might be another reason r the higher event rate in deep

lesions [19]. Studies to validate these hypotheses have not been done.

The growth of CMs is related to repeated intralesional hemorrhage, thrombosis, and subsequent organization and
recanalization [21,43,50]. Enlargement of hemorrhagic cysts, deposition of hemosiderin, recanalization of thrombi
with formation of new vascular channels, and reactive gliosis may all add to the bulk of the lesion [21]. Repeated
intralesional microhemorrhages and their breakdown products can also initiate a series of responses such as cellular
proliferation, fibrosis, calcification, and gliosis that promote new vessel formation and coalescence (hemorrhagic
angiogenic proliferation) [9,21]. The leaky vessels produced by this reactive angiogenesis and the neovascularization
of hemorrhagic cysts lead to further microscopic or gross hemorrhages that perpetuate the cycle and result in growth
of the lesion. These changes in the lesion may or may not have clinical manifestations.

Figure 14. CM: fluid/fluid level. (A,B) Tl and T2 weighted NM imaging shows a cerebellar mass compressing the
fourth ventricle and surrounded by edema. The T I hyperintensity, T2 hypointensity, and fluid/fluid levels all
indicate subacute blood products.

Figure 15. CM: growth secondary to hemorrhage. (A,B)'I'2 weighted MR imaging shows a small hypointense lesion
on the initial scan (eirroA,) that increased in size (curved arrow) on the follow-up scan I year later. The interval
change in size and the development of surrounding edema indicates a hemorrhage. The patient had seizures only.

 Recovery from events

Several authors have studied recovery from neurologic events secondary to lesion activity. Tung et al reported that
an initial bleed caused only a transient deficit in 80% of patients [42]. They observed, however, that with each

subsequent hemorrhage, there is an increased chance of the patient ending up with a deficit, noting that all patients
with more than two bleeds had persistent neurologic deficits. In one study Porter et al reported that only one third of
patients experiencing an event will recover fully. One third of patients with events will have no significant recovery,
and one third will have, partial recovery [19]. This study reports that there is no difference in the degree of recovery
when comparing hemorrhagic versus nonhemorrhagic events, supratentorial versus infratentorial lesions, and deep
versus superficial locations. In an updated review of this same patient population, with more patients and a longer
follow-up, Porter et al [19] still found no difference in the recovery of patients from hemorrhagic versus
nonhemorrhagic events and between supratentorial versus infratentorial lesions. No difference was found in the
degree of recovery between superficial and deep lesions; 50% of patients with clinical events related to superficial
lesions completely recovered compared with only 33% of patients with deep lesions (P = 0.024).

Figure 16. Intraventricular cavernoma

MANAGEMENT

The recommendations for the management of patients with cavernous malformations have varied throughout the
years. In general surgery is hardly advised for superficial lesions because of the benign nature and course of
superficial lesions. Surgery is probably only indicated for seizure control in superficial lesions.

Deep lesions have a greater propensity to produce symptoms and deficits compared with superficial lesions.
Intuitively, therefore, management of these patients should be more aggressive, as the postoperative functional status
largely depends on the preoperative neurologic function. Logically, it would be beneficial to the patient to be treated
before any deficits arise from these deep lesions. Approaching lesions in the deep areas of the neuraxis, however,
particularly the brainstem, carries significant risk. Although several authors have reported good results with surgery
in terms of neurologic function, these results should be interpreted with caution, as these are highly selected series
[14,15,20,42,51]. In addition, lesions that do reach the pial or ependymal surface carry an even higher risk at surgery,
because eloquent tissue must be traversed to reach the lesion.

Radiosurgery of CMs has been considered to be an appealing alternative to surgery, particularly in the deep lesions.
The literature on radiosurgery of CMs is inconclusive. In 1995, Kondziolka et al reported on their series of 47
patients [17]. They quoted an annual hemorrhage rate of 56.5% (including the first bleed) and a subsequent
hemorrhage rate of 320/o/year. This high hemorrhage rate reflects the fact that this population was a highly selected
group, and hemorrhage was defined as any clinical or radiologic event. After treatment with radiosurgery, they
reported hemorrhage rates of 8.8% for the first two years, then 1. I %/year from two to six years. They concluded
that there is a latency of 2-3 years for the maximal effects of radiosurgery to take place, with the most benefit
experienced after 3.5 years [52]. Karisson et al [53], based on their experience at the Karolinska Institute, reported
that 9 out of 22 patients developed a hemorrhage after radiosurgery with the gamma knife, and 6 developed
radiation-induced complications, with 2 patients experiencing both. They quoted an 8.8% hemorrhage rate after
radiosurgery. They noted a trend for the hemorrhage rate to decrease four years after treatment. They reported that
there is a sevenfold increase in the occurrence of complications in the treatment of CMs when compared with
treating arteriovenous malformations with the same dose distribution. They concluded that the high incidence of
complications does not justify the limited protection the treatment provides in only exceptional cases [53]. Results
presented by Pollock et al [54] agree with those from the Karolinska group. They noted a 59% morbidity rate
(transient and permanent) after treatment and a 41% permanent radiation-related morbidity for CMs. Pollock et al

agree with Karlsson that whatever protection radiosurgery provides for these patients may not be worth the
significant occurrence of radiation-induced complications [54].

Present literature supports the fact that the hemorrhage rates after radiosurgery decrease after a latency of about
two to four years. This statement has to be qualified, however, as only a select group of patients benefit and a
significant number of patients experience permanent morbidity, either from hemorrhage after the treatment or from
radiation-induced necrosis. Also, the reduction in hemorrhage rates after treatment may actually reflect the natural
course of a CM after a bleed (caused by clustering of events), and not actual protection provided by the irradiation
[48,54]. Barker et al reported a monthly rehemorrhage rate of 2.0% during the first 2.5 years after an initial
symptomatic hemorrhage. This was followed by a decrease in the hemorrhage risk to less than 1% per month
without any treatment [48].

Patients with superficial CMs are advised of the benign course of their disease and are usually asked to come for
follow-up every one to two years, unless surgery is required for medically refractory seizures. Patients with deep
CMs are informed that clinical events are not uncommon, up to 10% per year. The risks, benefits, and possible
complications of surgery are discussed with patients who have deep lesions with pial or ependymal representation.
Symptomatic patients with lesions that have no pial nor ependymal representation are also considered for surgery.
For deep, symptomatic lesions that do not reach the pial or ependymal surfaces, we consider stereotactic
radiosurgery as a potential treatment modality, still of unproven value, and would encourage its use only in the
setting of a randomized, controlled trial that allows direct comparison to the natural history over time.

SUMMARY

SUMMARY

Cavernous malformations are commonly being recognized on CT and MR imaging in both asymptomatic and
symptomatic patients. The diagnosis of CMs can often be made on MR imaging based on the characteristic
morphology of the subacute and chronic blood products. An atypical appearance of a CM in the setting of a recent
hemorrhage requires follow-up imaging to confirm the diagnosis. Deep CMs have a significant clinical event rate that
justifies close follow up or surgical treatment if possible.

 Addendum

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Case record...Occipital lobe cavernoma

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