A 61 year old male developed progressive spastic tetraparesis and paresis of the lower cranial nerves (IX, X and XI) after a minor spine-head trauma. Magnetic resonance depicted a partially cystic IV ventricular mass, extending to C1/C2 level. Neuropathology was compatible with choroids plexus papilloma (CCP). This case shows a rare clinical presentation of an infrequent adult tumour.

Download full-text PDF

Source

Publication Analysis

Top Keywords

[unusual tetraparesis
4
tetraparesis adult]
4
adult] year
4
year male
4
male developed
4
developed progressive
4
progressive spastic
4
spastic tetraparesis
4
tetraparesis paresis
4
paresis lower
4

Similar Publications

Article Synopsis
  • Invasive breast cancer, particularly the no special type subtype, is the most common breast cancer, while lymphoma and melanoma are the primary tumors that spread to the breast.
  • Rhabdomyosarcoma (RMS) is a common pediatric soft-tissue cancer, rare in the breast, typically affecting adolescent girls and mostly presenting as the alveolar variant.
  • A case study of a 17-year-old girl highlights the unusual occurrence of RMS metastasizing to both breasts, initially misdiagnosed as tuberculosis affecting the spine, illustrating the difficulty in diagnosing such rare cases.
View Article and Find Full Text PDF

Tuberculous retropharyngeal abscess, though rare, poses significant diagnostic and therapeutic challenges due to its atypical presentation. We present the case of a 51-year-old male with a history of drug abuse and inhalational burn injury presented with generalized weakness, sensory deficits, and neurological symptoms. Despite initial negative investigations, subsequent MRI and microbiological studies confirmed a rare case of tuberculous retropharyngeal abscess.

View Article and Find Full Text PDF

We report unusual cases of combined central and peripheral demyelination in two siblings related to pregnancy, each presenting with progressive tetraparesis and cranial nerve palsies. The elder sister had a relapsing-remitting course with optic nerve dysfunction and died during a relapse from respiratory insufficiency. The younger sister presented with disorientation and acute-onset limb and facial weakness.

View Article and Find Full Text PDF
Article Synopsis
  • Guillain-Barré syndrome (GBS) is an autoimmune condition that leads to rapid muscle weakness and loss of reflexes, and it is acquired, not hereditary.
  • The case involves a 37-year-old male who experienced rapid progression of weakness in his lower and upper limbs, following a fever and gastrointestinal symptoms.
  • Unusually, he presented with some reflex activity in his arms and legs, contrary to typical GBS symptoms, and had nerve studies indicating a mixed type of neuropathy; he required immunotherapy but reacted negatively to the treatment.
View Article and Find Full Text PDF

Background: Pregnancy imposes significant physiological changes, including alterations in electrolyte balance and renal function. This is especially important because certain disorders might worsen and make people more susceptible to electrolyte abnormalities. One such condition is Sjogren's syndrome (SS), an autoimmune disease that can cause distal renal tubular acidosis (dRTA).

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!