Literature DB >> 19496942

MELAS with diffuse degeneration of the cerebral white matter: report of an autopsy case.

Teruo Yokoyama1, Kazuko Hasegawa, Runko Obama, Tadayuki Ishihara, Saburou Yagishita.   

Abstract

Up to now diffuse white matter demyelination of the cerebrum has been reported in only a few cases of mitochondrial encephalopathy with lactic acidosis and stroke-like episodes (MELAS). Here we document an autopsy case with this rare neuropathology. Most MELAS cases are diagnosed antemortem by A3243G transition of mitochondrial DNA. While cerebral damage including necrotic foci in the cerebral cortex are common findings in MELAS, prominent white matter involvement best characterizes this MELAS case. There were numerous necrotic foci, varying in size and chronological stage, in the cerebral white matter. In the areas of the white matter without necrotic foci, there was diffuse fibrillary gliosis with the loss of axons and oligodendrocytes. The gliosis was dominant in the deep white matter, sparing the U-fiber. The cerebral cortex showed diffuse cortical atrophy with few scattered necrotic foci. Distribution of the cerebral lesions does not coincide with the territory of blood supply. The vascular wall presented only slight to mild hyalinosis. We assumed a common pathogenesis to the cortical lesions and the white matter change. The pathogenesis of the present diffuse cerebral lesions may not be just secondary to circulatory disturbance but partly due to metabolic abnormality.

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Year:  2009        PMID: 19496942     DOI: 10.1111/j.1440-1789.2009.01026.x

Source DB:  PubMed          Journal:  Neuropathology        ISSN: 0919-6544            Impact factor:   1.906


  10 in total

1.  Voxelwise analysis of diffusion tensor imaging and structural MR imaging in patients with the m.3243A>G mutation in mitochondrial DNA.

Authors:  S M Virtanen; M M Lindroos; K Majamaa; P Nuutila; R J Borra; R Parkkola
Journal:  AJNR Am J Neuroradiol       Date:  2011-01-13       Impact factor: 3.825

2.  Acute Cortical Lesions in MELAS Syndrome: Anatomic Distribution, Symmetry, and Evolution.

Authors:  K D Bhatia; P Krishnan; H Kortman; J Klostranec; T Krings
Journal:  AJNR Am J Neuroradiol       Date:  2019-12-05       Impact factor: 3.825

3.  Thymidine Kinase 2 and Mitochondrial Protein COX I in the Cerebellum of Patients with Spinocerebellar Ataxia Type 31 Caused by Penta-nucleotide Repeats (TTCCA)n.

Authors:  Hanako Aoki; Miwa Higashi; Michi Okita; Noboru Ando; Shigeo Murayama; Kinya Ishikawa; Takanori Yokota
Journal:  Cerebellum       Date:  2022-01-27       Impact factor: 3.847

Review 4.  Stroke and Etiopathogenesis: What Is Known?

Authors:  Tiziana Ciarambino; Pietro Crispino; Erika Mastrolorenzo; Antonello Viceconti; Mauro Giordano
Journal:  Genes (Basel)       Date:  2022-05-30       Impact factor: 4.141

Review 5.  In Vivo NMR Studies of the Brain with Hereditary or Acquired Metabolic Disorders.

Authors:  Erica B Sherry; Phil Lee; In-Young Choi
Journal:  Neurochem Res       Date:  2015-11-26       Impact factor: 3.996

6.  Brain MRS correlates with mitochondrial dysfunction biomarkers in MELAS-associated mtDNA mutations.

Authors:  Laura L Gramegna; Stefania Evangelisti; Lidia Di Vito; Chiara La Morgia; Alessandra Maresca; Leonardo Caporali; Giulia Amore; Lia Talozzi; Claudio Bianchini; Claudia Testa; David N Manners; Irene Cortesi; Maria L Valentino; Rocco Liguori; Valerio Carelli; Caterina Tonon; Raffaele Lodi
Journal:  Ann Clin Transl Neurol       Date:  2021-05-05       Impact factor: 4.511

7.  Connectivity on fMRI in the MELAS brain may strongly depend on heteroplasmy and extension or dynamics of stroke-like lesions.

Authors:  Josef Finsterer
Journal:  Neuroimage Clin       Date:  2021-03-09       Impact factor: 4.881

8.  Comparative Analysis of Lipid Extracts and Imaging Mass Spectrometry for Evaluating Cerebral White Matter Biochemical Pathology in an Experimental Second-Hand Cigarette Smoke Exposure Model.

Authors:  Alexander Krotow; Emine B Yalcin; Jared Kay; Suzanne M de la Monte
Journal:  Mass Spectrom Purif Tech       Date:  2016-04-20

Review 9.  The non-syndromic clinical spectrums of mtDNA 3243A>G mutation.

Authors:  Xiya Shen; Ailian Du
Journal:  Neurosciences (Riyadh)       Date:  2021-04       Impact factor: 0.906

Review 10.  Monogenic Causes of Strokes.

Authors:  Justyna Chojdak-Łukasiewicz; Edyta Dziadkowiak; Sławomir Budrewicz
Journal:  Genes (Basel)       Date:  2021-11-23       Impact factor: 4.096

  10 in total

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