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Lhermitte-Duclos Disease Associated with Neurofibromatosis Type-1 and Non-Ossifying Fibroma

Lhermitte-Duclos disease (LDD) is a rare cerebellar disorder of uncertain pathogenesis characterized by enlargement of cerebellar folia. Magnetic resonance imaging is the diagnostic modality of choice and usually distinguishes the LDD by its characteristic "striated or laminated pattern" a...

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Published in:Acta radiologica (1987) 2005-02, Vol.46 (1), p.97-100
Main Authors: Yesilda, A., Baykal, B., Ayata, A., Kerman, G., Koroglu, M., Olgar, S., Oyar, O.
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cited_by cdi_FETCH-LOGICAL-c420t-a1a915c289a9256fee4542bf7c1eb6e48efa25e6420fa70963053a80fad4bd463
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container_title Acta radiologica (1987)
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creator Yesilda, A.
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Oyar, O.
description Lhermitte-Duclos disease (LDD) is a rare cerebellar disorder of uncertain pathogenesis characterized by enlargement of cerebellar folia. Magnetic resonance imaging is the diagnostic modality of choice and usually distinguishes the LDD by its characteristic "striated or laminated pattern" appearance. Various additional abnormalities have been reported in association with LDD. We report a case of LDD coexisting with neurofibromatosis type 1 (NF-1) and non-ossifying fibroma.
doi_str_mv 10.1080/02841850510020932
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subjects Biological and medical sciences
Bone Neoplasms - complications
Bone Neoplasms - diagnosis
Cerebellar Neoplasms - complications
Cerebellar Neoplasms - diagnosis
Child
Fibroma - complications
Fibroma - diagnosis
Ganglioneuroma - complications
Ganglioneuroma - diagnosis
Humans
Investigative techniques, diagnostic techniques (general aspects)
Male
Medical sciences
Neurofibromatosis 1 - complications
Neurofibromatosis 1 - diagnosis
Neurology
Tibia
Tumors of the nervous system. Phacomatoses
title Lhermitte-Duclos Disease Associated with Neurofibromatosis Type-1 and Non-Ossifying Fibroma
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