Cerebral Tumours

As a comparatively small proportion of tumours of the brain—using the term “tumour” in its widest sense—are amenable to surgical treatment, it is only necessary here to refer to those aspects of this subject that have a distinctively surgical bearing.

Various forms of growth occur in the brain, the most common being tuberculous nodules, syphilitic gumma, endothelioma, glioma, and sarcoma. Less frequently fibroma, osteoma, and parasitic, hæmorrhagic, and other cysts are met with. The growth may originate in the brain tissue primarily, or may spread thence from the membranes, or from the skull. In relation to operative treatment, it is an unfortunate fact that those forms that are well defined and do not tend to infiltrate the brain tissue, usually occur at the base, where they are difficult to reach; while those that develop in more accessible regions are for the most part infiltrating growths of a gliomatous or sarcomatous nature, and are therefore irremovable.

Clinical Features.—The presence of a tumour in the brain inevitably results sooner or later in an increase in the intra-cranial tension, and to this the symptoms are chiefly due.

The earliest and most prominent of the general symptoms are severe paroxysmal headache, optic neuritis, with choked disc and limitation of the field for blue, amounting sometimes to blue-blindness (Cushing). The relative degree of neuritis in the two eyes is a reliable guide to the side on which the tumour is situated (Horsley). The symptoms are seldom absent, and are common to all forms of tumour, wherever situated. Vomiting, which is without relation to the taking of food and is usually unattended by nausea, is a characteristic symptom when present, but it is wanting in two-thirds of the cases (Cushing). Vertigo, general convulsions, and signs of mental deterioration are also present in a considerable proportion of cases.

In addition, certain localising symptoms may be present. When, for example, the tumour is situated in the cortex of the Rolandic area, attacks of Jacksonian epilepsy, preceded by an aura, which is usually referable to the centre primarily implicated, are common. The group of muscles first involved, and the order in which other groups become affected, are important localising factors. As the tumour increases in size, these irritative phenomena are replaced by localised paralyses. The tactile and muscular sensations are also disturbed, and motor and sensory aphasia may be present. In some cases localised tenderness on percussing the skull may be of assistance in indicating the site of the tumour.

When the tumour is sub-cortical, that is, in the centrum ovale, there are no Jacksonian spasms, the motor paralysis is more widespread, and sensation also is lost on the opposite side of the body. There is no special tenderness on percussion. It is not always possible, however, to distinguish between cortical and sub-cortical tumours, and in many cases both areas are invaded.

Tumours situated in the region of the internal capsule, and in the deeper parts of the brain, are not attended with Jacksonian spasms, paralysis develops more rapidly than in cortical and sub-cortical tumours, and there is complete loss of sensation on the opposite side of the body. The cranial nerve-trunks also are liable to be pressed upon.

Tumours and cysts in the cerebellum give rise to symptoms similar to those of cerebellar abscess ([p. 381]).

Tumours in the cerebello-pontine angle, in addition to the special symptoms associated with cerebellar lesions, give rise to symptoms of interference with nerve-roots of the same side. The facial and acoustic nerves are most frequently affected, resulting in facial weakness, tinnitus, loss of perception for high-pitched notes, as tested by Galton's whistle, or absolute unilateral deafness. Any of the other cranial nerves from the fifth to the twelfth may be either irritated or paralysed. Pressure on the pons may produce hemiplegia of the opposite side, with spasticity and exaggeration of reflexes. Sudden death may occur from crowding of the cerebellum into the foramen magnum.