Zobrazeno 1 - 10
of 145
pro vyhledávání: '"Dysplastic Cerebellar Gangliocytoma"'
Autor:
Amro Abdelrahman, MBBS, Shahd M. Abass, MBBS, Elhassan M. Abdalla, MBBS, Shuhal Elamin, MBBS, Hany A. Zaki, MD, Khalid Y. Fadul, MBBS, Muhammad Abugabala, MBBS, Mohamed Elgassim, MD
Publikováno v:
Radiology Case Reports, Vol 19, Iss 7, Pp 2820-2825 (2024)
Lhermitte-Duclos disease (LDD) is a rare, slow-growing neoplasm that develops in the brain's posterior fossa. It can appear as a single lesion or as part of Cowden's syndrome.We report the case of a 51-year-old female with a history of diabetes, hype
Externí odkaz:
https://doaj.org/article/ce33e63bc25a470d96f4653911fb6025
Publikováno v:
Romanian Journal of Neurology, Vol 23, Iss 1, Pp 87-90 (2024)
Lhermitte–Duclos disease (LDD), also known as dysplastic cerebellar gangliocytoma, is an uncommon hamartomatous lesion found in the cerebellar cortex. First described by French physicians Lhermitte and Duclos in 1920, this condition involves enlarg
Externí odkaz:
https://doaj.org/article/b0ced1e8755b40b0a08f0c79afe50983
Autor:
Hanane El Aggari, MD, Siham Nasri, MD, Ahsayen Fatima Zohra, MD, Narjisse Aichouni, MD, Imane Kamaoui, MD, Imane Skiker, MD
Publikováno v:
Radiology Case Reports, Vol 18, Iss 8, Pp 2763-2767 (2023)
The dysplastic gangliocytoma of the cerebellum, also known as Lhermitte-Duclos disease, is an uncommon hamartomatous lesion in the posterior fossa with some distinctive neuroradiological characteristics. It can happen in combination with Cowden syndr
Externí odkaz:
https://doaj.org/article/60c8a2dc875b4f54afe1d7d5e05635fd
Akademický článek
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Publikováno v:
Nepal Journal of Neuroscience, Vol 16, Iss 3, Pp 68-71 (2019)
Lhermitte–Duclos Disease is a rare entity characterized by diffuse or focal enlargement of cerebellar folia. Clinical manifestations are usually related to a mass effect and secondary obstructive hydrocephalus. Increased intracranial pressure sympt
Externí odkaz:
https://doaj.org/article/e81987085a9949a899b55b7e71df6a04
Publikováno v:
Formosan Journal of Surgery, Vol 52, Iss 5, Pp 197-199 (2019)
Cowden syndrome (CS) is a rare genetic disease which puts patients at an increased risk of developing mucocutaneous lesion, multiple hamartomas, breast cancer, thyroid cancer, and Lhermitte–Duclos disease (LDD). This article reviews the role of LDD
Externí odkaz:
https://doaj.org/article/cf8fe50a897d4f06a16a703e5f1ac02b
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Publikováno v:
Quant Imaging Med Surg
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a255a9d5ba270f6cf44f432d7c8acdc3
https://doi.org/10.21037/qims-20-627
https://doi.org/10.21037/qims-20-627
Publikováno v:
SN Comprehensive Clinical Medicine. 3:2373-2377
Cowden syndrome (CS) is a rare, autosomal dominant, multisystem disease related to the mutation of phosphatase and tensin homolog (PTEN) tumor suppressor gene. It is characterized by the occurrence of multiple hamartomas and mucocutaneous lesions and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::25ee53be73035a5e6f95e2247e8ecc28
https://doi.org/10.1007/s42399-021-01015-x
https://doi.org/10.1007/s42399-021-01015-x
Autor:
Salah Bellasri, Soufiane Belabbas
Publikováno v:
The Pan African Medical Journal, Vol 28, Iss 51 (2017)
A 42-year-old female presented with complaints of mild occipital headaches of severe months duration. There were no cutaneous lesions or significant family history suggesting any genetic disease. On examination, she did not have any papilloedema, dym
Externí odkaz:
https://doaj.org/article/2661f3c076a94964a09f00aef40f27ca