Gangliocitoma displásico del cerebelo (Enfermedad de Lhermitte-Duclos) asociado a Síndrome de Cowden
نویسندگان
چکیده
منابع مشابه
Cowden disease with Lhermitte-Duclos disease: case report.
BACKGROUND We report a case and review the recent literature describing 36 patients with both Lhermitte-Duclos disease (LDD) and Cowden disease (CD). Lhermitte-Duclos disease, or dysplastic gangliocytoma, is a benign hamartomatous condition involving the cerebellum. The presenting symptoms are usually headaches, gait ataxia, and symptoms of lower cranial nerve involvement. Cowden disease is a r...
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Desde hace años, el estudio de las funciones visuoperceptivas y visuomotoras ha adquirido un gran interés en la valoración de las capacidades mentales. Entre las diversas pruebas existentes para la evaluación de estas funciones, la tarea de dibujar un reloj, más conocida como test del reloj (TR), ha suscitado un notable interés por su fácil aplicación así como por la información que podemos obt...
متن کاملLhermitte - duclos Disease :
Lhermitte-Duclos disease (LDD) is a benign neoplasm of posterior fossa, involving cerebellum. It is also known as dysplastic cerebellar gangliocytoma. It is not a true neoplasm but a hamartoma. It can be either isolated finding or associated with Cowden (multiple hamartoma syndrome). adults.
متن کاملLhermitte-Duclos disease.
Lhermitte-Duclos disease was first described in 1920 in the literature under the names of Purkinjeoma, granular cell hypertrophy of the cerebellum, hamartoma of the cerebellum, dysplastic gangliocytoma, ganglioneuroma, and gangliomatosis of the cerebellum. Patients tend to be young adults and may present with signs of cerebellar dysfunction or increased intracranial pressure secondary to obstru...
متن کاملLhermitte-Duclos disease.
Lhermitte-Duclos disease (dysplastic gangliocytoma of the cerebellum) is a rare benign cerebellar mass of unknown etiology which is characterized by enlargement of the cerebellar folia. Despite the controversy regarding its pathogenesis, imaging and histopathological findings are rather typical. A 17-year-old female presented with a 2-year history of progressive headaches and gait imbalance. Cr...
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ژورنال
عنوان ژورنال: Revista médica (Colegio de Médicos y Cirujanos de Guatemala)
سال: 2020
ISSN: 2664-3677,2074-7004
DOI: 10.36109/rmg.v159i1.166