Keywords
pineal gland cavernous angioma - cavernous hemangioma - pineal region
Introduction
Cavernous angioma is a vascular malformation that usually presents as agglomerates
of blood vessels that have a histological characteristic on the vascular walls, and
absence of elastic coating, with little or no intervention of the cerebral tissue.
They are lesions circumscribed to the interior of the nervous parenchyma.[1]
[2]
The most common sites of this lesion are the cerebral hemispheres, followed by the
brainstem, the cavernous sinus, the basal ganglia and the thalamus. Considered a disease
most commonly reported in females, its diagnosis is usually made after neurological
manifestations related to the location of the angiomas. Thus, focal deficits, headache
and seizures may occur. Accidental imaging findings are frequently observed in asymptomatic
patients.[1]
[3]
[4]
Magnetic resonance imaging (MRI) is an imaging technique that has a greater sensitivity
for the detection of angiomas,[5] and it shows a typical image of a T2-weighted peripheral hypodense ring suggestive
of hemosiderin, as well as the interior of the lesion with a heterogeneous characteristic.[5]
[6]
Surgical removal makes it possible to cure cavernous angioma, and is the most advised
technique to avoid the complications of the natural evolution of this lesion, especially
hemorrhage.[1]
[3]
[7] Guided stereotactic surgery is considered safer and rapid for the total resection
of subcortical and deep cerebral cavernous angiomas.[1]
The cavernous angioma surrounding the pineal gland has a probability of occurrence < 1%.[7] The first reported case of angioma in the pineal gland was in 1961; the malformation
was partially removed, and the patient died after an episode of cerebral hemorrhage.
From that date until the year 2010, 21 cases of cavernous angioma in the pineal gland
region were reported.[3]
[7]
The present study reports a case of cavernous angioma in the topography of the pineal
gland, with supratentorial hydrocephalus, in which a complete surgical resection was
chosen.
Due to the infrequency of cavernous angioma in the pineal gland region, and because
it is a curable lesion, studies that seek to deepen the knowledge of this disease
are relevant.
Case Report
E.Z.F.I, a 67-year-old woman, presented an incipient blurred vision and was evaluated
by an ophthalmologist, who did not observe alterations in the examination. The patient
had improvement in the period of 60 days, but, 2 months after this period, she presented
mental confusion, bilateral visual acuity deficit and progressive gait ataxia associated
with retrograde amnesia and inversion of the sleep and wake cycle, remaining sleepy
during most of the day and alert at night. There was worsening in the nocturnal insomnia,
mental confusion, and gait ataxia, which consequently restricted her to the bed and
the wheelchair; thus, she needed help to perform her basic routine activities.
Three weeks later, she presented a fall from her own height, and was then referred
and admitted for evaluation in the emergency room. There was no report of worsening
in the consciousness level, vomiting or trauma-related headache. Upon admission, the
patient presented ocular opening responding to simple commands, she was confused,
disoriented regarding time and space, with periods of psychomotor agitation. The pupils
were isocoric and had preserved photoreactive reflex. Although it did not cooperate
adequately with the neurological examination, absence of motor deficit was observed
with the active mobilization of the four limbs. Extrinsic ocular motility also did
not reveal apparent changes; however, the patient presented bilateral visual acuity
deficit. When positioned to ambulate, she presented ataxic gait with postural instability.
A head computed tomography (CT) scan, performed at admission, revealed significant
dilatation of the ventricular system. There was a hyperdense expansive lesion with
hemorrhagic appearance located in the topography of the mesencephalon ceiling in the
pineal gland region, which caused supratentorial obstructive hydrocephalus.
An MRI scan, performed after contrast injection, confirmed the presence of a macrolobulated
expansive lesion affecting the topography of the pineal gland, and measuring 17 × 24 × 17
mm. The lesion presented a hypersignal in T1 ([Fig. 1]) with a hyposignal mark in the susceptibility weighted imaging SWI sequence, suggesting
blood content as well as moderate contrast uptake.
Fig. 1 Magnetic resonance imaging scan of the brain after contrast injection. Hypersignal
on T1.
This lesion caused obliteration of the cerebral aqueduct, with consequent obstruction
of the suprathoracic ventricles ([Fig. 2]) associated with the moderate ependymal transudation revealed by the hypersignal
in T2 ([Fig. 3]) and the fluid-attenuated inversion recovery (FLAIR) of the periventricular white
matter. The diagnostic impression of the radiologist was of an expansive germinal
lesion.
Fig. 2 Magnetic resonance imaging scan of the brain after contrast injection. Obstruction
of the ventricular system.
Fig. 3 Magnetic resonance imaging scan of the brain after contrast injection. Hypersignal
on T2 revealed ependymal transudation.
We chose to perform microsurgery with supratentorial, supracerebellar inter-hemispheric
access. During the surgical procedure, the left lateral ventricle was punctured with
the placement of an external ventricular derivation (EVD). The operative finding was
a violaceous and capsulated lesion. The microsurgical incision of the lesion revealed
its content, with organized clots and a discrete amount of nervous tissue. The report
of the anatomopathological examination of the intraoperative frozen sections was compatible
with cavernous angioma, and the lesion was completely removed.
In the postoperative period, the patient was gradually awakened in the intensive care
unit (ICU). The EVD was kept open for cerebrospinal fluid (CSF) drainage. A CT scan
of the skull for postoperative control revealed improvement in ventricular dilatation,
total removal of the angioma, and pneumocephalus. The patient was extubated and presented
progressive improvement in the level of consciousness and visual acuity. The EVD was
closed after 48 hours, and the patient did not present alterations in the neurological
picture. The EVD was removed, and the patient was discharged from the ICU. A new CT
scan of the skull was performed, and it showed absence of hydrocephalus and elimination
of the pneumocephalus ([Fig. 4]). On the subsequent days, the patient presented neurological improvement and was
discharged from the hospital; she was alert, oriented, and ambulating with assistance.
There was an improvement in visual acuity and normal extrinsic ocular motricity. The
definitive anatomopathological report was compatible with an arteriovenous malformation:
cavernous angioma.
Fig. 4 Computed tomography scan of the skull showing absence of hydrocephalus and pneumocephalus.
Discussion
Cavernous angioma is a vascular malformation that accounts for 5 to 13% of lesions
in the central nervous system.[7] Histologically, it presents thin walls of endothelial cells separated by fibrous
collagen, and no elastic coating, with little or no intervention of the cerebral parenchyma.[1]
[2]
The etiology of cavernous angioma is still a subject of discussion, but there is evidence
that this lesion is derived from an autosomal dominant inheritance located on chromosome
7,[8] and there is still the possibility of radiotherapy-induced cavernous angioma.[5] The formation of radiotherapy-induced cavernous angioma is relatively infrequent,
and usually occurs in pediatric patients.[6] The most characteristic sites of cavernous angiomas are the cerebral hemispheres,
the brainstem, the cavernous sinus, the basal ganglia and the thalamus.[4] Supratentorial lesions comprise 80 to 90% of the cases; infratentorial lesions,
15%; and lesions in the spinal cord, 5%. Of the total cavernous malformations, 9 to
35% occur in the brainstem,[9] and the probability of involvement of the pineal gland region is < 1%.[5]
The risk of hemorrhage in cavernous angiomas varies according to the location: those
lesions located more deeply, such as those in the brainstem, thalamus or basal ganglia,
present a risk of 4.1%; in the cases of superficial craniomas, 0.4%,[5]
[9] whereas the risk of hemorrhage in the region of the pineal gland is quite small.[3] Regardless of the area affected by the cavernous angioma, an initial hemorrhage
significantly increases a new episode of hemorrhage.[5] Studies have shown that female patients have a higher incidence of bleeding, probably
due to hormonal changes.[4]
The patient in the case reported here presented with bleeding visualized on the MRI
scan ([Figs. 1] and [2]), but it is not possible to determine if this event was the first bleeding, since
there are no prior examinations for comparison.
Magnetic resonance imaging is the method of choice for the detection and diagnosis
of cavernous angioma because it is a more sensitive examination.[5] The characteristic image of a cavernous angioma includes a low-intensity, more sensitive
T2-weighted peripheral ring due to the deposition of hemosiderin in the surrounding
parenchyma, a result of small hemorrhages that most commonly exhibit a mixed intensity
nucleus on both T1 and T2 images. ([Fig. 2]). These characteristics may vary depending on the imaging sequences, as they are
determined by the blood products within the lesion and by the surrounding hemosiderin
ring. Although it is an excellent tool for diagnosis, it is advisable to complement
it with other sequences of images for a more precise definition of the lesion.[10]
The clinical diagnosis of this disease is difficult, since it can be confused with
other lesions in the pineal gland,[3] as it frequently occurs in cases of pineocytomas and pineoblastomas, but especially
in cases of germ-cell tumors.[3] This usually happens because the germ cells are more localized characteristic in
the pineal gland or neurohypophysis, and the occurrence of germ-cell tumors is greater
than that of cavernous angiomas in this region, varying from 4 to 9%.[11]
The clinical manifestations related to the disease vary; a common manifestation is
the sign of Parinaud, characterized mainly by difficulty in vertical ocular movement;
other manifestations may be signs of intracranial hypertension, headache, visual disturbances,
gait ataxia, and altered circadian rhythm. In addition, there are still signs of hemiparesis,
hemi-hypoesthesia, diabetes insipidus, and amenorrhea with elevated prolactin. Neuroendocrine
disorders occur mainly due to damage to the hypothalamus region by distension of the
floor of the third ventricle.
Cavernous angioma located in the pineal gland is usually accompanied by supratentorial
hydrocephalus with dilation of the lateral ventricles and third ventricle, and the
fourth ventricle is preserved. There may be, though more rarely, an obstruction of
the aqueduct through a dilated subependymal vein, functioning as a venous channel
for the angioma.[12] Patients who develop obstruction of the aqueduct, causing hydrocephalus, may present
intracranial hypertension with headache, mental confusion and relegation of the level
of consciousness.[3]
[4]
For the treatment of supratentorial hydrocephalus, from the case reported here, an
EVD was performed. Another method that could be chosen is the third ventriculostomy,
considered to be less invasive and with visual control of procedures. This method
is seen as a simple procedure unless there is anatomical variation in the floor of
the third ventricle, especially in cases of long-standing hydrocephalus, and it also
contributes as a less infectious form when compared with external ventricular drain.[13]
[14]
[15]
The surgery for the total removal of the cavernous angioma from the case reported
here was performed by supracerebellar supratentorial interhemispheric access due to
the surgeon's experience and to the anatomical particularity of the region, which
enabled safe access to the pineal gland following the cerebral falx and tentorium.
Other surgical techniques could be used, such as intraoperative localization (neuronavigation)
or stereotactic surgery.[16]
Despite the surgeon's choice, stereotactic surgery has been the most used approach
for cavernous angiomas, because the mortality of these surgeries is very low, ∼ 2%.
The choice of approach is usually made by verification of the brain tissue enveloped
in the structures, based on imaging exams such as the MRI. The main postoperative
complications are hemorrhages and neurological deficits.[17]
The most advanced technology is neuronavigation surgery, which consists of the use
of an equipment capable of associating images of the patient's MRI with real-time
magnetoencephalogram images, giving the surgeon greater precision, since he/she has
access to the anatomy, and the possibility of better planning for access and approach
routes.[18]
Complete removal of the cavernous angioma enables the healing of this type of lesion,
and is also the most advisable technique to avoid the complications that this malformation
can lead to with its natural evolution, such as recurrent bleeding, convulsions and
neurological deficits.
Conclusion
Based on this study, it is considered important that the occurrence of cavernous angioma,
although rare, be evaluated in the diagnoses of cases of lesions in the pineal gland.
In the case reported here, we verified that the surgical approach associated with
the control of the hydrocephalus is a safe option for the treatment of this disease.
