Leptomeningeal amyloidosis due to A25T TTR mutation: a case report.

نویسندگان

  • L Llull
  • J Berenguer
  • J Yagüe
  • F Graus
چکیده

12. Restelli L, Moretti MP, Pellerin I, Galante G, Castiglioni C. Transcutaneous electrical nerve stimulation and neuralgic facial pain. Pain Clinic. 1988;2:97—103. 13. Pareja JA, Pareja J, Yangüela J. Nummular headache, trochleitis, supraorbital neuralgia, and other epicranial headaches and neuralgias: the epicranias. J Headache Pain. 2003;4:125—31. 14. Mulero P, Guerrero AL, Pedraza M, Herrero-Velázquez S, de la Cruz C, Ruiz M, et al. Non-traumatic supraorbital neuralgia. A clinical study of 13 cases. Cephalalgia. 2012;32:1150—3. 15. Caminero AB, Mateos V. Aproximación clínica a las neuralgias craneales. Rev Neurol. 2009;48:365—73. L. López Mesonero , M.I. Pedraza Hueso, S. Herrero Velázquez, A.L. Guerrero Peral

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Leptomeningeal amyloidosis due to A25T TTR mutation: A case report

12. Restelli L, Moretti MP, Pellerin I, Galante G, Castiglioni C. Transcutaneous electrical nerve stimulation and neuralgic facial pain. Pain Clinic. 1988;2:97—103. 13. Pareja JA, Pareja J, Yangüela J. Nummular headache, trochleitis, supraorbital neuralgia, and other epicranial headaches and neuralgias: the epicranias. J Headache Pain. 2003;4:125—31. 14. Mulero P, Guerrero AL, Pedraza M, Herrer...

متن کامل

Successful Diflunisal Desensitization in a Transthyretin Amyloidosis Patient with NSAID Allergy: A Case Report

Introduction: Amyloid diseases have been known to be hereditary, including transthyretin (TTR) amyloidosis where subunit protein mutations may occur in genes for TTR leading to the deposition of fibrils (low molecular weight subunits (5 to 25 kD) of proteins) in extracellular tissues. By reducing the formation of TTR amyloid, diflunisal, a nonsteroidal anti-inflammatory drug (NSAID), has shown ...

متن کامل

Transthyretin Leu12Pro is associated with systemic, neuropathic and leptomeningeal amyloidosis.

We report a middle-aged woman with a novel transthyretin (TTR) variant, Leu12Pro. She had extensive amyloid deposition in the leptomeninges and liver as well as the involvement of the heart and peripheral nervous system which characterizes familial amyloid polyneuropathy caused by variant TTR. Clinical features attributed to her leptomeningeal amyloid included radiculopathy, central hypoventila...

متن کامل

Familial leptomeningeal amyloidosis with a transthyretin variant Asp18Gly representing repeated subarachnoid haemorrhages with superficial siderosis.

OBJECTIVES To report the clinical features of two Japanese brothers with familial leptomeningeal amyloidosis, showing a causative gene abnormality of a transthyretin (TTR) variant Asp18Gly, previously reported only in a Hungarian family. METHODS The authors reported on a 42 year old man (patient 1) and his 45 year old brother (patient 2), both suffering from subarachnoid haemorrhage (SAH) wit...

متن کامل

PiB-PET detects transthyretin-related cerebral amyloid angiopathy.

Transthyretin (TTR) is an amyloidogenic protein synthesized primarily (.95%) by the liver and, to a lesser extent, by the choroid plexuses and retinal pigment epithelium. Hereditary TTR amyloidosis (ATTR) is a multisystem disorder that may manifest with 3 main clinical phenotypes: familial amyloid polyneuropathy (FAP), familial amyloid cardiomyopathy, and familial leptomeningeal amyloidosis. TT...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:
  • Neurologia

دوره 29 6  شماره 

صفحات  -

تاریخ انتشار 2014