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Biomedical subjects

J Wislawski

Publications and source records attributed to J Wislawski.

At least 19 recordsLinked to original sources

Cytostatics for acromegaly. Marked improvement in a patient with an invasive pituitary tumour.

A 21-year-old woman suffering from acromegaly was treated with transsphenoidal subtotal hypophysectomy (microscopy: acidophilic adenoma), followed by x-ray and bromocriptine therapy. Seven years later she was re-operated because of a partial bitemporal loss of vision, intracranial hypertension, and regrowth of the pituitary tumour seen on CT-scan. A large part of the invasive suprasellar tumour was then removed by transcranial approach. The neurosurgery was followed by cobalt radiotherapy and bromocriptine administration. Two years later, symptoms and signs of tumour growth reappeared. Administration of cytostatics, such as doxorubicin (Adriamycin) and lomustine (Belustine), resulted in distinct clinical improvement associated with a seven-fold decrease in the serum growth hormone concentration. The visual field became normal and the intracranial mass on a CT scan decreased markedly. As a result the patient was able to resume work.

Acromegaly↗

Jadassohn's naevus phakomatosis: I. A report of two cases.

Two typical cases of Jadassohn's Naevus Phakomatosis are reported, with full clinical details, history and the results of investigations. Neurosurgery was necessary in one case so that the macroscopical appearance of the brain and histological findings of portions of the brain removed are described.

Adolescent↗

[Cerebral and cerebellar ependymomas in children].

Clinical analysis of 63 cerebral and cerebellar ependymomas in children aged up to 14 years showed that in the initial period of the disease the diagnosis based only on clinical manifestations may be difficult, before the appearance of signs of raised intracranial pressure eintraventricular or paraventricular ependymomas may cause attacks of vomiting, abdominal pains or signs of meningeal irritation. In every case with supposed brain tumour the child should be referred to a specialist since the results are better in earlier diagnosed and treated cases. Histological examination of biopsy material showed presence of 5 types of ependymonas: 1. with numerous cells (63%), 2 mixed (15%), 3 malignant (11%), 4 subependymal (4%), 5, epithelial (3%). In cases with subtotal removal of the tumour the mean survival is 12 months. After radical operation of the tumour the longest survival was 16 years.

Adolescent↗