A Radiological Curiosity of a Rare Diagnosis: Lhermitte-Duclos Disease

Lhermitte–Duclos disease (LDD) is a rare cerebellar lesion, described in 1920 by two French physicians: Lhermitte and Duclos. The clinical presentation is usually made of neurological symptoms. This lesion is characterized by a hamartomatous lesion in the posterior fossa. Mainly diagnosed by MRI, wh...

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Published in:Asian journal of oncology Vol. 8; no. 3; pp. 136 - 139
Main Authors: Wilson Bizimana, Rita Oze Koudouhonon, Suzanne Rita Aubin Igombe, Waïs A. Amarkak, Khadija Benelhosni, Ittimade Nassar, Nabil Billah Moatassim
Format: Journal Article
Language:English
Published: Thieme Medical Publishers, Inc 17-10-2022
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Abstract Lhermitte–Duclos disease (LDD) is a rare cerebellar lesion, described in 1920 by two French physicians: Lhermitte and Duclos. The clinical presentation is usually made of neurological symptoms. This lesion is characterized by a hamartomatous lesion in the posterior fossa. Mainly diagnosed by MRI, when it comes to preoperative, the T2-weightened MRI demonstrates the classical “tiger-striped” pattern. The definitive diagnosis, nonetheless, is histopathological. The treatment for LDD consists of surgical decompression or excision. We present here a rare case of a woman who developed neurological symptoms that led to LDD diagnosis to describe protocol MRI imaging, the main findings and their pathophysiological meanings.
AbstractList Lhermitte–Duclos disease (LDD) is a rare cerebellar lesion, described in 1920 by two French physicians: Lhermitte and Duclos. The clinical presentation is usually made of neurological symptoms. This lesion is characterized by a hamartomatous lesion in the posterior fossa. Mainly diagnosed by MRI, when it comes to preoperative, the T2-weightened MRI demonstrates the classical “tiger-striped” pattern. The definitive diagnosis, nonetheless, is histopathological. The treatment for LDD consists of surgical decompression or excision. We present here a rare case of a woman who developed neurological symptoms that led to LDD diagnosis to describe protocol MRI imaging, the main findings and their pathophysiological meanings.
Author Nabil Billah Moatassim
Khadija Benelhosni
Suzanne Rita Aubin Igombe
Rita Oze Koudouhonon
Wilson Bizimana
Waïs A. Amarkak
Ittimade Nassar
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  fullname: Wilson Bizimana
  organization: Central Radiology Department, UHC Ibn SINA, Mohamed V. University, Rabat, Morocco
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  fullname: Rita Oze Koudouhonon
  organization: Central Radiology Department, UHC Ibn SINA, Mohamed V. University, Rabat, Morocco
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  fullname: Suzanne Rita Aubin Igombe
  organization: Central Radiology Department, UHC Ibn SINA, Mohamed V. University, Rabat, Morocco
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  fullname: Waïs A. Amarkak
  organization: Central Radiology Department, UHC Ibn SINA, Mohamed V. University, Rabat, Morocco
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  fullname: Khadija Benelhosni
  organization: Central Radiology Department, UHC Ibn SINA, Mohamed V. University, Rabat, Morocco
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  fullname: Ittimade Nassar
  organization: Central Radiology Department, UHC Ibn SINA, Mohamed V. University, Rabat, Morocco
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  fullname: Nabil Billah Moatassim
  organization: Central Radiology Department, UHC Ibn SINA, Mohamed V. University, Rabat, Morocco
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Snippet Lhermitte–Duclos disease (LDD) is a rare cerebellar lesion, described in 1920 by two French physicians: Lhermitte and Duclos. The clinical presentation is...
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SubjectTerms cerebellum
lhermitte duclos disease
tiger striping sign
Title A Radiological Curiosity of a Rare Diagnosis: Lhermitte-Duclos Disease
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