Ruptured Berry Aneurysm

Histoire cliniqueUne femme de 62 ans s’est présentée avec une désorientation dans le temps, le lieu et la personne. L’examen clinique ne révélait aucun signe neurologique localisé. L’imagerie a montré une lésion occupant l’espace au niveau du plancher du 3ème ventricule. Un prélèvement tissulaire a été réalisé lors de la chirurgie, mais l’exérèse complète n’a pas été possible. L’histologie a confirmé un craniopharyngiome. En postopératoire, la patiente a développé des dérèglements métaboliques complexes, probablement d’origine hypothalamique. Son état s’est progressivement aggravé et elle est décédée dix semaines après son admission, suite à une aspiration gastrique.PathologieLe cerveau sectionné sagittalement montre une tumeur ovoïde rose-gris de 2,5 x 1,5 cm, centrée dans la région de l’hypothalamus. La tumeur est encapsulée sauf au pôle ventral où un tissu a été retiré lors d’une intervention précédente. La coupe montre un aspect microkystique ou spongieux. La tumeur déforme le 3ème ventricule et obstrue le foramen de Monro. Le chiasma optique est déplacé vers le bas. Un shunt ventriculo-atrial antérieur a empêché la dilatation des ventricules latéraux malgré cette obstruction. Informations complémentairesLes craniopharyngiomes représentent 1-3 % de tous les tumeurs cérébrales et 5-10 % chez l’enfant, avec une distribution bimodale d’âge entre 5-14 ans et 50-75 ans. Leur incidence est plus élevée au Japon et en Afrique. Ce sont des tumeurs épithéliales, généralement issues de la tige pituitaire, mais peuvent aussi provenir de la selle turcique, du système optique ou du 3ème ventricule. Elles comportent souvent des composantes solides et kystiques, ces dernières contenant des cristaux de cholestérol. Deux types principaux existent : adamantinome et papillaire, différant par leur histologie et leur génétique, bien que l’impact pronostique soit incertain. Le traitement associe résection chirurgicale et radiothérapie pour traiter la maladie résiduelle. Le pronostic dépend du contrôle tumoral et des complications locales ou endocriniennes.

Clinical HistoryA 73-year-old woman was admitted with new left-sided hemiplegia. On further questioning, she reported a 3-month history of headaches, nausea, and worsening balance. CT identified an inoperable brain tumour. She passed away one week after admission.Pathology A coronal brain slice reveals a poorly demarcated tumour in the right temporal lobe, causing hemispheric enlargement and flattening of the gyri. The posterior view shows subfalcine herniation, and the mass displays areas of necrosis and haemorrhage. Histology confirmed an astrocytoma, Grade III/IV. Further InformationAstrocytomas are a subtype of glioma, the second most common CNS cancer after meningioma. Originating from astrocytes, they are classified by grade—diffuse (II), anaplastic (III), to glioblastoma (IV). Typical histology shows gemistocytes with eosinophilic cytoplasm against a fibrillary background. Most occur in the hemispheres of patients aged 40–60 and present with seizures, headaches, nausea, or focal deficits. Without treatment, median survival for Grade III tumors is ~~18 months. Management involves surgery, radiotherapy, chemotherapy, or combinations tailored to the patient.

Clinical HistoryOver a 3-year period, a 57-year-old woman experienced intermittent frontal headaches and memory disturbances that progressed to psychiatric symptoms, vomiting, and meningeal signs. Localising neurological signs appeared only late in the disease course.Pathology A coronal section of the cerebral hemisphere reveals a round, haemorrhagic, variegated tumour in the left temporal lobe. Tumour tissue extends across the midline, replacing the corpus callosum and nearly obliterating the ventricular system. Further sections confirmed these lesions are part of one massive tumour. Further Information Gliomas are the second most common CNS cancer after meningiomas. These tumours resemble normal macroglial cells—astrocytes, oligodendrocytes, and ependymal cells—and arise from progenitor cells differentiating along these lines. Glioblastoma multiforme (GBM), a grade IV astrocytoma, can develop de novo or from lower-grade gliomas. Histologically, GBMs feature necrosis surrounded by anaplastic cells and hyperplastic blood vessels. GBMs are more frequent in males and typically diagnosed in the 6th decade. Risk factors include neurofibromatosis type 1, Li-Fraumeni syndrome, and prior brain radiotherapy. Symptoms depend on tumour location and include persistent headaches, visual disturbances, vomiting, appetite loss, mood and personality changes, cognitive decline, new seizures, and speech difficulties. Diagnosis relies on CT and MRI. About 50% of GBMs involve more than one hemisphere and often invade ventricular walls or meninges, occasionally reaching the CSF. Metastases outside the CNS are rare. Tumour growth causes cerebral oedema and increased intracranial pressure. These aggressive tumours have a median survival of around 3 months if untreated. Treatment includes surgery, radiation, and chemotherapy.

Clinical HistoryA 56-year-old male presented with a generalised seizure after which he remained unconscious and later died. A history revealed 6 months of progressive confusion, short-term memory loss, and personality changes.PathologyPost-mortem coronal brain sections show a 4 cm necrotic and haemorrhagic tumour invading from the inferior frontal lobe into the lateral ventricle. Meningeal spread is visible on the posterior aspect. Further InformationGliomas are the second most common central nervous system cancers after meningiomas. They originate from glial-like cells such as astrocytes, oligodendrocytes, or ependymal cells. Glioblastoma multiforme (GBM), a grade IV astrocytoma, arises from astrocytes and may develop de novo or from lower-grade tumours. GBMs typically show necrosis surrounded by anaplastic cells and hyperplastic blood vessels. More frequent in males, GBM commonly occurs in the 6th decade. Risk factors include neurofibromatosis type 1, Li-Fraumeni syndrome, and prior brain radiotherapy. Symptoms depend on tumour location and include persistent headaches, visual disturbances, vomiting, appetite loss, mood and personality changes, cognitive decline, seizures, and speech difficulties. Diagnostic tools are CT and MRI. About 50% of GBMs involve more than one hemisphere, often invading ventricles or meninges, with rare spinal cord spread. Metastasis outside the CNS is uncommon. Tumour growth leads to cerebral oedema and increased intracranial pressure. These aggressive tumours have a median survival of approximately 3 months if untreated. Treatment consists of surgery followed by radiation and chemotherapy.

Clinical HistoryThis 51-year-old woman had undergone surgery for breast carcinoma two years before presenting with left-sided ataxia of two weeks’ duration. A previous fainting episode followed by weakness on the same side had preceded this. Examination revealed left spastic paresis. Due to the rapid onset of symptoms, a vascular lesion was suspected. Despite discharge, she was re-admitted six weeks later with left-sided seizures. Lumbar puncture and clinical re-evaluation were inconclusive, but EEG showed a right anterior temporal abnormality. Angiography then revealed a large space-occupying lesion in the right cerebrum. Her condition continued to deteriorate, ultimately resulting in death.PathologyThe horizontal brain slice reveals three cystic tumours, predominantly in the right parietal region. The largest measures 5 cm in diameter. Another tumour is seen near its posterior margin, and a third, smaller one is found in the left parietal region. The tumours mainly affect the white matter, with shaggy, friable greyish tissue walls. The largest tumour had ulcerated into the right lateral ventricle, and subfalcine herniation with displacement of the basal ganglia and internal capsule was observed. Histology confirmed metastatic carcinoma. Additional metastases were found in the liver and bone, consistent with a primary breast carcinoma.

Clinical HistoryIn the 1970s, a 31-year-old woman presented with severe headache and diplopia, eight months after the removal of an invasive pigmented skin melanoma from her neck. Initial clinical examination revealed no abnormalities. She was discharged but re-admitted later with persistent vomiting. Her condition rapidly deteriorated, and she died shortly after.PathologyThe brain specimen shows extensive intracerebral melanoma metastases. The inferior surface displays numerous dark nodules up to 1.5 cm in diameter. On the cut superior surface, similar lesions are visible and confined to the grey matter. The tumour nodules are not encapsulated and infiltrate the cortex, with areas of necrosis and haemorrhage present. Further InformationMelanoma accounts for about 10% of all brain metastases. Risk increases with age over 60, male gender, disease progression, and certain genetic mutations such as BRAF or NRAS. Most metastases are supratentorial and may present with headache, neurological deficits or seizures. These lesions have a known risk of spontaneous haemorrhage. Diagnosis is based on imaging and histological confirmation. Treatment often involves stereotactic radiosurgery, radiotherapy, and systemic immunotherapy or targeted therapies, improving median survival to around 11 months in recent years.

Clinical HistoryAn 80-year-old man suddenly lost consciousness. On examination, there was a right gaze palsy, left hemiplegia, and right hemiparesis.Pathology Coronal sections at the level of the mammillary bodies, including the brainstem and anterior temporal lobes, show a massive clot replacing tissue in the left basal ganglia and internal capsule. The haemorrhage ruptured into the left lateral ventricle and temporal horn, destroying its walls and infiltrating adjacent brain. The right lateral ventricle is also filled with blood but retains intact walls. The clot acts as a space-occupying lesion, expanding the left hemisphere and shifting midline structures rightward. A subfalcine herniation of the left cingulate gyrus under the falx cerebri is evident. Further Information Intracerebral haemorrhages of this type commonly result from systemic hypertension. The bleed arises from the rupture of a micro-aneurysm in striate artery branches supplying the basal ganglia.

Clinical HistoryThis 58-year-old patient died due to post-operative complications following transurethral resection of the prostate. He had experienced two episodes of transient neurological deficits at the ages of 28 and 35. At 50, he developed a permanent hemiparesis affecting the left leg, primarily the ankle.PathologyThis coronal brain slice through the parietal lobes reveals a 4 cm lesion in the medial right hemisphere, extending from the cortical surface to the lateral ventricle. The abnormal area consists of tortuous vascular channels and interspersed tissue. Histology confirmed an arteriovenous malformation (AVM) with glial tissue surrounding vessels of both arterial and venous character. Further InformationCerebral AVMs can cause a range of symptoms such as headaches, seizures, and cranial nerve deficits, though some patients remain asymptomatic. In serious cases, vessel rupture may lead to intracranial haemorrhage, resulting in loss of consciousness, nausea, vomiting, and vision problems. Neurological deficits like hemiparesis or aphasia may occur depending on the bleed location. Ruptured AVMs carry significant risks of both mortality and long-term disability.

Clinical HistoryA 56-year-old woman with a 6-month history of intermittent headaches and vomiting was admitted to hospital in a comatose state following a grand mal seizure. She did not regain consciousness.Pathology This coronal brain section reveals that the brain has been compressed laterally and downward due to a large intracranial mass on the right side, likely a meningioma (though the tumour itself is not present in the section). The anterior view shows a midline shift with subfalcine herniation of the cingulate gyrus. The posterior view displays haemorrhages of varying ages in the temporal lobe and pons, which are typical for a supratentorial mass lesion. There is also noticeable ventricular asymmetry. Further Information A space-occupying meningioma can exert pressure on brain tissue, resulting in atrophy and displacement, which in turn may affect cranial nerve function, blood flow, and normal brain processes. Common symptoms may include: - Seizures – such as myoclonic (brief muscle jerks or spasms) or tonic-clonic (loss of consciousness, muscle rigidity, followed by convulsions and potential loss of body control). - Sensory disturbances – changes in vision, smell, or hearing without loss of consciousness.The presentation can vary depending on the tumour’s location.