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C Oliveras

Publications and source records attributed to C Oliveras.

13 recordsLinked to original sources

[Paraneoplastic encephalomyelitis and Lambert-Eaton syndrome].

In two men presenting with muscle weakness and disturbances of equilibrium neurophysiological examination by repeated stimulations revealed responses suggestive of Lambert-Eaton syndrome. In the first month of the disease very high levels of anti-Hu antibody were found in the serum and CSF, betraying a malignant lesion. This was confirmed by autopsy 4 months later in one patient and by bronchial biopsy 16 months later in the other patient. Both had small-cell lung carcinoma associated with paraneoplastic encephalomyelitis.

Aged

[Heart block].

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Bundle-Branch Block

[Lumbosacral spinal cord infarction. Data from magnetic resonance imaging].

A 77-year old woman and a 61-year old man with lumbosacral spinal cord ischaemic lesions and paraplegia presented with dissociated or partial forms of the lumbar enlargement artery (Adamkiewicz's artery) syndrom. Magnetic resonance imaging (MRI) was performed in both patient with an 0.15 Tesla resistive magnet. A hypersignal on T2-weighted images was present in both cases, which corresponded to the infarction affecting the lumbosacral part of the cord. MRI provided accurate delineation of the lesions and clinicoradiological correlations in both patients. The hypersignal occupied the lumbar cord in case 1 and the conus medullaris in case 2. The clinical signs and location of the lesions seemed to be determined by the different patterns of lumbosacral arterial supply. Since such images could be confused with tumoral images, surgical exploration was carried out in both patients; it failed to demonstrate any tumour or cyst and only showed a pale cord. Surgical cord biopsy in case 2 demonstrated ischaemic tissue. We conclude that ischaemia of the spinal cord can be demonstrated by MRI, but owing to the low specificity of this imaging method aedema cannot be distinguished from necrosis, gliosis or demyelination.

Aged

[Neurosyphilis in patients infected with the human immunodeficiency virus].

Nervous central system involvement is observed in two out of three patients infected with human immunodeficiency virus and probably, the true prevalence is even higher than that clinically detected. The coexistence of neurosyphilis in this group of patients has been poorly studied and the possibility that some alterations in the natural history of syphilis related to its rapid course with respect to time in which neurologic involvement would occur would have reasonable immunologic basis. We report two patients aged 26 and 22 who presented antibodies against human immunodeficiency virus together with meningo-vascular syphilis with spinal involvement and secondary brain infarction, respectively. In both patients, neurosyphilis was the first manifestation of human immunodeficiency virus infection and none of them referred a history of previous primary or secondary syphilis.

Acquired Immunodeficiency Syndrome