M. Zahlane

A migraine as initial presentation of celiac disease

Celiac disease (CD), also known as gluten-sensitive enteropathy, is a prevalent auto-immune disorder. The silent form of CD seems to be more frequent than expected. CD has been associated with neurologic and psychiatric disorders, notably cerebellar ataxia, peripheral neuropathy, epilepsy, dementia and depression. Migraine is a rare complication of CD. We report a case of CD revealed by a migraine. Apparently no case of celiac disease revealed by migraine has been reported in the literature.

Intracranial aneurysm revealing a HIV infection and resolving with highly active antiretroviral therapy

These lesions are commonly seen in children and young adults, with no gender difference.[5] The exact pathogenesis is unclear, but it could be due to a trapped adipocyte during embryogenesis, during the neural tube formation stage. This is thus a hamartoma rather than a true neoplasm.[6] These are slow growing tumors, which cause progressive symptoms over the years. The clinical presentation is usually a long duration of nonspecific symptoms, which then progress to numbness, altered gait, spasticity of the limbs and bowel or bladder disturbances. MRI remains the best investigation, not only for a diagnosis, but also for knowing the extent of the lesion and its relation with the cord.[7] Microsurgical excision with or without duroplasty is the treatment of choice. Surgery, however, may be limited by the adherence of the lipoma to the cord, due to the encapsulated nerve roots, and hence, subtotal excision with regular follow-up is the best option. Figure 3: Postoperative MRI showing near total excision with expanded spinal cord and remnants of lipoma at the superior and inferior margins Figure 2: H and E stain showing lobules of mature adipose tissue (lipoma) Yam B. Roka, M. Shrestha1, P. R. Puri, Hari B. Adhikari Departments of Neurosurgery, and 1Anesthesiology, Neuro Hospital, Jahada Road, Biratnagar-13, Nepal E-mail: dryamroka@yahoo.com

Une céphalée migraineuse révélant une maladie cœliaque : à propos d’un cas

u stade de cirrhose au moment du diagnostic. Des manifestaions auto-immunes associées ont été retrouvées chez 23 patients 71,87 %) et étaient dominées par la thyroïdite auto-immune et e syndrome de Goujerot-Sjogren. Un syndrome de chevaucheent a été retenu dans 17 cas (50 %), associant Cirrhose biliaire rimitive-HAI (46,8 %) ou cholangite sclérosante primitive-HAI 6,25 %). Vingt patients ont été traités. Le traitement a consisté ans tous les cas en l’association corticoïdes-azathioprime. La émission complète a été obtenue chez 19 patients (95 %). Dix our cent des sujets ont récidivé après un délai moyen de 2 mois. Une décompensation œdémato-ascitique de la cirrhose st survenue chez 3 patients présentant tous un syndrome de hevauchement. onclusion.– En Tunisie, le profil épidémiologique et clinique des alades atteints d’une HAI est similaire à celui rapporté dans la ittérature mais avec un taux plus élevé de cirrhose au moment du iagnostic.