Neuropathology and general autopsy findings in AIDS during the last 15 years.

Abstract:

:A retrospective study of 450 consecutive AIDS autopsy cases (397 males, 53 females; mean age at death 38.4 years) in Vienna, Austria, between 1984 and 1999 compares the central nervous system (CNS) findings in three cohorts: 1984-1992 (190 cases), 1993-1995 (162 cases) and 1996-1999 (98 cases, after introduction of triple antiretroviral therapy) and the relationship of CNS findings to systemic AIDS pathology in the latter two cohorts. In these two groups, following involvement of the lung (85% and 75%, respectively), the brain continued to be the second most frequently involved organ (decrease from 80% to 60%, respectively). Extracerebral protozoal (Pneumocystis carinii, toxoplasmosis), Mycobacterium avium complex, viral [e.g., cytomegalovirus (CMV)], multiple opportunistic organ and CNS infections, and Kaposi sarcoma significantly decreased over time. There was less decrease in fungal infections, while bacterial organ and CNS infections (except for mycobacteriosis), lymphomas, HIV-associated CNS lesions (around 30%), non HIV-associated changes (vascular, metabolic, etc.) and negative CNS findings (10-11%) remained unchanged. Nonspecific CNS changes (e.g., meningeal fibrosis) increased. Extracerebral pathology in subjects with advanced HIV-related CNS lesions showed more frequent but decreasing systemic bacterial and CMV infections than those with negative or nonspecific neuropathology, while other opportunistic and multiple organ infections and lymphomas showed no differences between both groups. In a cohort of drug abusers, HIV encephalitis, progressive multifocal leukoencephalopathy, bacterial infections, hepatic encephalopathy, and negative CNS findings were more frequent than in non-users who showed increased incidence of CMV, toxoplasmosis, or other opportunistic CNS infections, and nonspecific CNS findings; the frequency of lymphomas was similar in both drug abusers and non-users. Similar to a recent autopsy study from San Diego, these data suggest that despite the beneficial effects of modern antiretroviral combination therapy, involvement of the brain in AIDS subjects continues to be a frequent autopsy finding, while the increased incidence of HIV encephalitis in our small cohort of drug users was less than observed in other recent autopsy studies.

journal_name

Acta Neuropathol

journal_title

Acta neuropathologica

authors

Jellinger KA,Setinek U,Drlicek M,Böhm G,Steurer A,Lintner F

doi

10.1007/s004010000245

subject

Has Abstract

pub_date

2000-08-01 00:00:00

pages

213-20

issue

2

eissn

0001-6322

issn

1432-0533

journal_volume

100

pub_type

杂志文章
  • Artificial intelligence in neurodegenerative disease research: use of IBM Watson to identify additional RNA-binding proteins altered in amyotrophic lateral sclerosis.

    abstract::Amyotrophic lateral sclerosis (ALS) is a devastating neurodegenerative disease with no effective treatments. Numerous RNA-binding proteins (RBPs) have been shown to be altered in ALS, with mutations in 11 RBPs causing familial forms of the disease, and 6 more RBPs showing abnormal expression/distribution in ALS albeit...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/s00401-017-1785-8

    authors: Bakkar N,Kovalik T,Lorenzini I,Spangler S,Lacoste A,Sponaugle K,Ferrante P,Argentinis E,Sattler R,Bowser R

    更新日期:2018-02-01 00:00:00

  • The node of Ranvier in CNS pathology.

    abstract::Healthy nodes of Ranvier are crucial for action potential propagation along myelinated axons, both in the central and in the peripheral nervous system. Surprisingly, the node of Ranvier has often been neglected when describing CNS disorders, with most pathologies classified simply as being due to neuronal defects in t...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章,评审

    doi:10.1007/s00401-014-1305-z

    authors: Arancibia-Carcamo IL,Attwell D

    更新日期:2014-08-01 00:00:00

  • Plaque-type deposition of prion protein in the damaged white matter of sporadic Creutzfeldt-Jakob disease MM1 patients.

    abstract::Plaque-type deposition of prion protein (PrP) in the brain has been extremely rare in sporadic Creutzfeldt-Jakob disease patients with methionine homozygosity at polymorphic codon 129 of the PrP gene and type 1 abnormal isoform of PrP (sCJD-MM1). Here we report three sCJD-MM1 patients who showed prominent PrP-positive...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/s00401-008-0425-8

    authors: Kobayashi A,Arima K,Ogawa M,Murata M,Fukuda T,Kitamoto T

    更新日期:2008-11-01 00:00:00

  • High binding of CS2 sulphur in spinal cord axonal fraction.

    abstract::The binding of carbon disulphide sulphur was studied in the spinal cord and its axons of four control and four phenobarbitone pretreated adult rats 3 and 6 h after an intraperitoneal injection of 650 mumol of CS2 in olive oil. The binding of CS2 carbon was measured in the same fractions of two adult control rats 4.5 h...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/BF00685369

    authors: Savolainen H,Vainio H

    更新日期:1976-11-15 00:00:00

  • Focal lesions area feature of chronic inflammatory demyelinating polyneuropathy (CIDP).

    abstract::In a study designed to identify the neuropathological features typical of chronic inflammatory demyelinating polyneuropathy (CIDP), we reviewed the sural nerve biopsy findings in 105 patients with this disorder. The patients' mean age at biopsy was 49 years. In 65% of patients the disease had a progressive and in 35% ...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/s004010050941

    authors: Rizzuto N,Morbin M,Cavallaro T,Ferrari S,Fallahi M,Galiazzo Rizzuto S

    更新日期:1998-12-01 00:00:00

  • Glioblastoma-related gene mutations and over-expression of functional epidermal growth factor receptors in SKMG-3 glioma cells.

    abstract::Amplification of the epidermal growth factor receptor (EGFR) gene is found in about 40% of glioblastomas (GBMs) but is rarely detected in GBM cell lines. We confirmed that the exceptional SKMG-3 GBM cell line retained amplified EGFR genes in vitro, and found that these sequences were concentrated on extra-chromosomal ...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/s004010000332

    authors: Thomas C,Ely G,James CD,Jenkins R,Kastan M,Jedlicka A,Burger P,Wharen R

    更新日期:2001-06-01 00:00:00

  • Alpha-synuclein accumulation in a case of neurodegeneration with brain iron accumulation type 1 (NBIA-1, formerly Hallervorden-Spatz syndrome) with widespread cortical and brainstem-type Lewy bodies.

    abstract::We studied a 27-year-old woman who died after a 6-year history of progressive dementia, dystonia, ataxia, apraxia, spasticity, choreoathetosis, visual and auditory hallucinations, and optic atrophy. Magnetic resonance imaging showed decreased intensity in the globus pallidus, substantia nigra, and dentate nuclei in T2...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/s004010000224

    authors: Neumann M,Adler S,Schlüter O,Kremmer E,Benecke R,Kretzschmar HA

    更新日期:2000-11-01 00:00:00

  • Spongy degeneration of the central nervous system in kittens.

    abstract::The paper describes the clinical and morphological features of a congenital neurological disease affecting two in-bred litter-mate kittens. The principal neurological features were ataxia and dysmetria. In one of the kittens light microscopy revealed widespread vacuolation of white and grey matter of the brain and spi...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/BF00690561

    authors: Kelly DF,Gaskell CJ

    更新日期:1976-06-15 00:00:00

  • Incidence and spectrum of sporadic Creutzfeldt-Jakob disease variants with mixed phenotype and co-occurrence of PrPSc types: an updated classification.

    abstract::Six subtypes of sporadic Creutzfeldt-Jakob disease with distinctive clinico-pathological features have been identified largely based on two types of the abnormal prion protein, PrP(Sc), and the methionine (M)/valine (V) polymorphic codon 129 of the prion protein. The existence of affected subjects showing mixed phenot...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/s00401-009-0585-1

    authors: Parchi P,Strammiello R,Notari S,Giese A,Langeveld JP,Ladogana A,Zerr I,Roncaroli F,Cras P,Ghetti B,Pocchiari M,Kretzschmar H,Capellari S

    更新日期:2009-11-01 00:00:00

  • Increased expression of neuregulin-1 in differentiating muscle satellite cells and in motoneurons during muscle regeneration.

    abstract::Neuregulins belong to a family of multipotent growth-promoting proteins, and have been shown to have a crucial role in accumulating acetylcholine receptor at neuromuscular junctions. A functional role of neuregulins in muscle regeneration has not yet been identified. Using reverse transcription (RT)-PCR, Western blot ...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/s00401-007-0198-5

    authors: Hirata M,Sakuma K,Okajima S,Fujiwara H,Inashima S,Yasuhara M,Kubo T

    更新日期:2007-04-01 00:00:00

  • Gamma-enolase and glial fibrillary acidic protein in nervous system tumors. An immunohistochemical study using specific monoclonal antibodies.

    abstract::A large series of central and peripheral nervous system tumors was studied for the presence of glial fibrillary acidic protein (GFAP) and gamma-enolase (neuron-specific enolase, NSE), using specific monoclonal antibodies (mAbs). Occurrence in and specificity of GFAP to glial and mixed tumors was confirmed and depended...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/BF00687791

    authors: Cras P,Martin JJ,Gheuens J

    更新日期:1988-01-01 00:00:00

  • Reversibility of neurofilamentous inclusion formation following repeated sublethal intracisternal inoculums of AlCl3 in New Zealand white rabbits.

    abstract::In this report, we describe the clinical, topographical and immunohistochemical characteristics of neurofilament (NF) inclusion formation induced by the intracisternal inoculation of young adult New Zealand white rabbits at 28-day intervals with 100 micrograms AlCl3 over the course of 267 days. The ability to recover ...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/BF00294460

    authors: Strong MJ,Gaytan-Garcia S,Jakowec DM

    更新日期:1995-01-01 00:00:00

  • Glial and neuronoglial malformative lesions associated with medically intractable epilepsy.

    abstract::In a large series of 116 cortical resections for treatment of medically intractable epilepsy, 10 glial hamartomas and 11 neuronoglial malformative lesions were found. Glial hamartomas were astrocytic in 3 cases, oligodendrocytic in 6 and mixed oligoastrocytic in 1. Neuronoglial lesions corresponded to "focal cortical ...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/BF00296190

    authors: Vital A,Marchal C,Loiseau H,Rougier A,Pedespan JM,Rivel J,Vital C

    更新日期:1994-01-01 00:00:00

  • Endogenous oligodendroglial alpha-synuclein and TPPP/p25α orchestrate alpha-synuclein pathology in experimental multiple system atrophy models.

    abstract::Multiple system atrophy (MSA) is characterized by the presence of distinctive glial cytoplasmic inclusions (GCIs) within oligodendrocytes that contain the neuronal protein alpha-synuclein (aSyn) and the oligodendroglia-specific phosphoprotein TPPP/p25α. However, the role of oligodendroglial aSyn and p25α in the format...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/s00401-019-02014-y

    authors: Mavroeidi P,Arvanitaki F,Karakitsou AK,Vetsi M,Kloukina I,Zweckstetter M,Giller K,Becker S,Sorrentino ZA,Giasson BI,Jensen PH,Stefanis L,Xilouri M

    更新日期:2019-09-01 00:00:00

  • Secretory meningiomas are defined by combined KLF4 K409Q and TRAF7 mutations.

    abstract::Meningiomas are among the most frequent intracranial tumors. The secretory variant of meningioma is characterized by glandular differentiation, formation of intracellular lumina and pseudopsammoma bodies, expression of a distinct pattern of cytokeratins and clinically by pronounced perifocal brain edema. Here we descr...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/s00401-013-1093-x

    authors: Reuss DE,Piro RM,Jones DT,Simon M,Ketter R,Kool M,Becker A,Sahm F,Pusch S,Meyer J,Hagenlocher C,Schweizer L,Capper D,Kickingereder P,Mucha J,Koelsche C,Jäger N,Santarius T,Tarpey PS,Stephens PJ,Andrew Futreal P,

    更新日期:2013-03-01 00:00:00

  • Motor neuron disease with dementia combined with degeneration of striatonigral and pallidoluysian systems.

    abstract::This study concerns an autopsy case of motor neuron disease with dementia (MND-D) that exhibited unusual clinical and neuropathological findings. The patient was a Japanese man without any relevant family history who was 60 years old at the time of death. His clinical manifestation included character change at the age...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/s00401-001-0482-8

    authors: Sudo S,Fukutani Y,Matsubara R,Sasaki K,Shiozawa M,Wada Y,Naiki H,Isaki K

    更新日期:2002-05-01 00:00:00

  • Glial cytoplasmic inclusions in neurologically normal elderly: prodromal multiple system atrophy?

    abstract::In this study, we used immunohistochemistry to screen for alpha-synuclein pathology in the brains of 241 individuals without clinical evidence of neurologic disease, and discovered 36 cases (15%) with incidental Lewy bodies (LBs) and one case, a 96-year-old woman (0.4%), with inclusions similar to those seen in multip...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/s00401-008-0398-7

    authors: Fujishiro H,Ahn TB,Frigerio R,DelleDonne A,Josephs KA,Parisi JE,Eric Ahlskog J,Dickson DW

    更新日期:2008-09-01 00:00:00

  • Congenital lead encephalopathy in monkeys.

    abstract::Thirty-one squirrel monkey fetuses were exposed to lead acetate given to the mothers perorally during the last three-fourths or two-thirds of pregnancy. The mean maternal blood lead concentration of the group was 37 micrograms/100 ml and the individual means ranged from 22-82 micrograms/100 ml. Examination of the cent...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/BF00687421

    authors: Lögdberg B,Brun A,Berlin M,Schütz A

    更新日期:1988-01-01 00:00:00

  • On the biology of prions.

    abstract::Prions cause scrapie and Creutzfeldt-Jakob disease (CJD); these infectious pathogens are composed largely, if not entirely, of protein molecules. No prion-specific polynucleotide has been identified. Purified preparations of scrapie prions contain high titers (greater than or equal to 10(9.5) ID50/ml), one protein (Pr...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章,评审

    doi:10.1007/BF00687261

    authors: Prusiner SB,Gabizon R,McKinley MP

    更新日期:1987-01-01 00:00:00

  • A novel leukoencephalopathy associated with tau deposits primarily in white matter glia.

    abstract::A 79-year-old woman had a 10-year history of dementia, initially presenting as non-fluent aphasia. Magnetic resonance imaging showed frontal atrophy (left greater than right) and hyperintense foci within white matter. Neuropathologically, there was severe frontal atrophy due to cortical neuronal loss with spongy chang...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/s00401-003-0719-9

    authors: Powers JM,Byrne NP,Ito M,Takao M,Yankopoulou D,Spillantini MG,Ghetti B

    更新日期:2003-08-01 00:00:00

  • S-antigen immunoreactivity in human pineal glands and pineal parenchymal tumors. A monoclonal antibody study.

    abstract::Using a four-step immunoperoxidase (PAP) method and the monoclonal antibody MAbA9-C6 (MAbA9-C6), which defines an epitope of the retinal S-antigen (S-Ag), we investigated the S-Ag immunoreactivity in human fetal, newborn, infantile and adult pineal glands and in 13 human pineal parenchymal tumors. S-Ag immunoreactivit...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/BF00688043

    authors: Perentes E,Rubinstein LJ,Herman MM,Donoso LA

    更新日期:1986-01-01 00:00:00

  • Effects of methylmercury on neuroepithelial germinal cells in the developing telencephalic vesicles of mice.

    abstract::Methylmercury (MeHg) poisoning (20 mg/kg body weight) in embryonic mice resulted in significant reductions of mitotic indices in the neuroepithelial germinal cells of the telencephalon at the ventricular surface 4 to 12 h following intoxication. After 24 h, no significant difference in the mitotic indices was observed...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/BF00293454

    authors: Choi BH

    更新日期:1991-01-01 00:00:00

  • Sporadic four-repeat tauopathy with frontotemporal degeneration, parkinsonism and motor neuron disease.

    abstract::We report a sporadic tauopathy of 6-year duration in a 76-year-old woman. Her initial symptoms were asymmetrical parkinsonism and muscle weakness, with apraxia appearing 2 years later. The brain showed frontal and temporal cerebral atrophy; severe neuronal loss and gliosis were observed in the precentral cortex (loss ...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/s00401-005-1086-5

    authors: Piao YS,Tan CF,Iwanaga K,Kakita A,Takano H,Nishizawa M,Lashley T,Revesz T,Lees A,de Silva R,Tsujihata M,Takahashi H

    更新日期:2005-12-01 00:00:00

  • Combined molecular analysis of BRAF and IDH1 distinguishes pilocytic astrocytoma from diffuse astrocytoma.

    abstract::Separation of pilocytic astrocytoma from diffuse astrocytomas frequently poses problems mostly related to small sample size. Precise classification and grading are essential due to different therapeutic strategies prompted by diagnoses of pilocytic astrocytoma WHO grade I, diffuse astrocytomas WHO grade II or anaplast...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/s00401-009-0550-z

    authors: Korshunov A,Meyer J,Capper D,Christians A,Remke M,Witt H,Pfister S,von Deimling A,Hartmann C

    更新日期:2009-09-01 00:00:00

  • Antibody-induced generation of reactive oxygen radicals by brain macrophages in canine distemper encephalitis: a mechanism for bystander demyelination.

    abstract::The mechanism of inflammatory demyelination in canine distemper encephalitis (CDE) is uncertain but macrophages are thought to play an important effector role in this lesion. Serum and cerebrospinal fluid (CSF), containing anti-canine distemper virus and anti-myelin antibodies from dogs with CDE were tested for their ...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/BF00688176

    authors: Griot C,Bürge T,Vandevelde M,Peterhans E

    更新日期:1989-01-01 00:00:00

  • Clofibrate-induced myopathy in the rat.

    abstract::Rats were given daily injections of 0.2 or 0.5 g/kg chlorophenoxyisobutyrate (clofibrate) for 9 to 46 days. Lower leg muscles were studied with light and electron microscopy. Daily treatment with 0.5 g/kg of the drug for 26--46 days caused myopathic changes. ...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/BF00703319

    authors: Teräväinen H,Larsen A,Hillbom M

    更新日期:1977-08-16 00:00:00

  • Extracellular edema and glial response to it in the cerebellum of suckling rats with low-dose lead encephalopathy. An electron microscopic and immunohistochemical study.

    abstract::Newborn rats were exposed to daily intraperitoneal injections of 10 mg lead nitrate per kg body weight for the first 15 postnatal days. The growth and mortality of the lead-exposed animals did not differ from their control litter-mates, injected with vehicle only. In our previous studies, focal hemorrhages and spongy ...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/BF00687071

    authors: Sundström R,Kalimo H

    更新日期:1987-01-01 00:00:00

  • Relative growth and maturation of axon size and myelin thickness in the tibial nerve of the rat. 1. Normal animals.

    abstract::Morphometric observations have been made on the medial plantar division of the tibial nerve (MPD) and on the motor branches of the tibial nerve to the calf muscles (MBC) in rats ranging in age from weaning (3 weeks) to 12 months. Axon size, assessed by measurements of circumference and cross-sectional area, increased ...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/BF00308712

    authors: Fraher JP,O'Leary D,Moran MA,Cole M,King RH,Thomas PK

    更新日期:1990-01-01 00:00:00

  • Cell surface aggregation of elastin receptor molecules caused by suramin amplified signals leading to proliferation of human glioma cells.

    abstract::We have recently shown that glioma cell lines, as well as cells of human malignant gliomas in situ, synthesize tropoelastin. In addition, glioma cells degrade tropoelastin using metalloproteinase(s), and the resulting peptides, incapable of assembling in the extracellular fibers, interact with the 67-kDa cell surface ...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/s004010051004

    authors: Hinek A,Jung S,Rutka JT

    更新日期:1999-04-01 00:00:00

  • Selective formation of certain advanced glycation end products in spinal cord astrocytes of humans and mice with superoxide dismutase-1 mutation.

    abstract::Recent studies have documented carbonyl stress involvement in the pathogenesis of sporadic amyotrophic lateral sclerosis (ALS). The aim of the present study was to assess a role for carbonyl stress in motor neuron degeneration associated with superoxide dismutase-1 (SOD1) mutant familial ALS and its transgenic mouse m...

    journal_title:Acta neuropathologica

    pub_type: 杂志文章

    doi:10.1007/s00401-002-0537-5

    authors: Shibata N,Hirano A,Hedley-Whyte ET,Dal Canto MC,Nagai R,Uchida K,Horiuchi S,Kawaguchi M,Yamamoto T,Kobayashi M

    更新日期:2002-08-01 00:00:00