Cytology of Equine Cerebrospinal Fluid

1983 ◽  
Vol 20 (5) ◽  
pp. 553-562 ◽  
Author(s):  
J. Beech

The cytology of cerebrospinal fluid samples from horses is described. The samples were obtained from 24 normal horses. 35 horses with axonal degeneration and/or spinal cord compression. 29 horses with encephalomyelitis, 14 horses with other lesions of the nervous system, and eight horses with signs of neurologic dysfunction of undetermined origin. (Three of the latter were suspected botulinum intoxications.) Fluid was aspirated from the atlanto-occipital space following general anesthesia or immediately after a lethal dose of barbiturate. In two horses, fluid also was aspirated from the lumbosacral space. Small mononuclear cells were predominant in normal horses, and in most horses with axonal degeneration and encephalomyelitis. Several horses with encephalomyelitis also had neutrophils, eosinophils, and some mitotic figures. Although the cytologic findings were abnormal in many of the horses with disease of the central nervous system, in most horses the cytologic findings were normal.

Author(s):  
Peggy Mason

The central nervous system develops from a proliferating tube of cells and retains a tubular organization in the adult spinal cord and brain, including the forebrain. Failure of the neural tube to close at the front is lethal, whereas failure to close the tube at the back end produces spina bifida, a serious neural tube defect. Swellings in the neural tube develop into the hindbrain, midbrain, diencephalon, and telencephalon. The diencephalon sends an outpouching out of the cranium to form the retina, providing an accessible window onto the brain. The dorsal telencephalon forms the cerebral cortex, which in humans is enormously expanded by growth in every direction. Running through the embryonic neural tube is an internal lumen that becomes the cerebrospinal fluid–containing ventricular system. The effects of damage to the spinal cord and forebrain are compared with respect to impact on self and potential for improvement.


2001 ◽  
Vol 69 (10) ◽  
pp. 6545-6548 ◽  
Author(s):  
Jun Fujii ◽  
Yoshimasa Kinoshita ◽  
Takashi Yutsudo ◽  
Hatsumi Taniguchi ◽  
Tom Obrig ◽  
...  

ABSTRACT The action of Shiga toxin (Stx) on the central nervous system was examined in rabbits. Intravenous Stx1 was 44 times more lethal than Stx2 and acted more rapidly than Stx2. However, Stx1 accumulated more slowly in the cerebrospinal fluid than did Stx2. Magnetic resonance imaging demonstrated a predominance of Stx1-dependent lesions in the spinal cord. Pretreatment of the animals with anti-Stx1 antiserum intravenously completely protected against both development of brain lesions and mortality.


2018 ◽  
Vol 23 (1) ◽  
pp. 69-72
Author(s):  
Antônio Santos De Araújo Júnior ◽  
Arnaldo Salvestrini Júnior ◽  
Pedro Alberto Arlani ◽  
Orlando Parisi ◽  
Mirella Martins Fazzito ◽  
...  

Introduction: Most hemangiopericytomas (HPC) are located in the musculoskeletal system and the skin, while the location in the central nervous system (CNS) is rare. Objective and Methods: We describe a patient suffering from a spinal extradural huge HPC, with marked spinal cord compression, extending from C6 to T3 level, who was elected to surgery. Results: Patient was submitted to surgery, via a posterior approach, indentifying a huge red-brown firm mass, highly vascular, that was softly dissected from surrounding tissues. Total gross removal was accomplished, with “in-block” resection, preserving neurological function, as shown by somatosensitive evoked potential. Histopathological examination and immunohistochemistry essay were performed confirming the diagnosis of Hemangiopericytoma. Conclusion: Spinal HPCs respond to approximately 8% of all HPC, tend to occur isolated and attached to spinal duramater, and usually present a good surgical cleavage between the tumor and the dura.


2022 ◽  
Vol 19 (1) ◽  
Author(s):  
Yi Kung ◽  
Kuan-Yu Chen ◽  
Wei-Hao Liao ◽  
Yi-Hua Hsu ◽  
Chueh-Hung Wu ◽  
...  

Abstract Background The blood-cerebrospinal fluid (CSF) barrier (BCSFB) is critically important to the pathophysiology of the central nervous system (CNS). However, this barrier prevents the safe transmission of beneficial drugs from the blood to the CSF and thus the spinal cord and brain, limiting their effectiveness in treating a variety of CNS diseases. Methods This study demonstrates a method on SD rats for reversible and site-specific opening of the BCSFB via a noninvasive, low-energy focused shockwave (FSW) pulse (energy flux density 0.03 mJ/mm2) with SonoVue microbubbles (2 × 106 MBs/kg), posing a low risk of injury. Results By opening the BCSFB, the concentrations of certain CNS-impermeable indicators (70 kDa Evans blue and 500 kDa FITC-dextran) and drugs (penicillin G, doxorubicin, and bevacizumab) could be significantly elevated in the CSF around both the brain and the spinal cord. Moreover, glioblastoma model rats treated by doxorubicin with this FSW-induced BCSFB (FSW-BCSFB) opening technique also survived significantly longer than untreated controls. Conclusion This is the first study to demonstrate and validate a method for noninvasively and selectively opening the BCSFB to enhance drug delivery into CSF circulation. Potential applications may include treatments for neurodegenerative diseases, CNS infections, brain tumors, and leptomeningeal carcinomatosis.


2019 ◽  
Author(s):  
Iva Vassileva Vesselinova

Myelomeningocele is the most common and severe congenital malformation of the central nervous system, associated with substantial neurological morbidity, devastating lifelong medical disability and increased mortality. This review focuses on the perioperative anesthesia considerations of postnatal correction of myelomeningocele. This contains 3 tables, and 34 references. Key words: myelomeningocele, Arnold Chiari malformation, tethered spinal cord syndrome, hydrocephalus, cerebrospinal fluid, ventriculo-peritoneal shunt, latex hypersensitivity, morbidity, mortality.


Author(s):  
Mark Harrison

This chapter describes the anatomy of the central nervous system as it applies to Emergency Medicine, and in particular the Primary FRCEM examination. The chapter outlines the key details of the structure, anatomy, and arteries of the cerebral hemispheres, blood supply and venous drainage, brainstem, cerebrospinal fluid, cerebellum, spinal cord, and core blood supply. This chapter is laid out exactly following the RCEM syllabus, to allow easy reference and consolidation of learning.


1992 ◽  
Vol 82 (1) ◽  
pp. 93-97 ◽  
Author(s):  
D. G. Weir ◽  
A. M. Molloy ◽  
J. N. Keating ◽  
P. B. Young ◽  
S. Kennedy ◽  
...  

1. Pigs were maintained in air or in an atmosphere of nitrous oxide which dramatically changes the S-adenosyl-l-methionine to S-adenosyl-l-homocysteine ratio in neural tissues. Samples of cerebrospinal fluid, cortex, cerebellum and spinal cord were then extracted and analysed for S-adenosyl-l-methionine and S-adenosyl-l-homocysteine. Regression analyses were carried out on values obtained in cerebrospinal fluid and in neural tissues. 2. Highly significant correlations were obtained between levels of S-adenosyl-l-homocysteine (r2 = 0.42-0.69; P < 0.001) and S-adenosyl-l-methionine/S-adenosyl-l-homocysteine ratios (r2 = 0.56-0.65; P < 0.001) in cerebrospinal fluid and levels and ratios in cortex, cerebellum and spinal cord. The levels of S-adenosyl-l-methionine did not show a significant correlation. 3. We conclude that the ratio of these metabolites in the cerebrospinal fluid may reflect the ratio in the central nervous system and we suggest that this may also be true in human tissues. This finding will permit the determination of the probable methylation ratio in the central nervous system in human conditions, such as vitamin B12 deficiency and acquired immune deficiency syndrome, where a similar myelopathy occurs to that seen in the nitrous oxide-treated pig. All three myelopathies may arise from an inhibition of methyltransferases involved in the synthesis of myelin that would occur when the methylation ratio is reduced.


1955 ◽  
Vol 184 (1) ◽  
pp. 220-222 ◽  
Author(s):  
Peter H. Wolff ◽  
Robert D. Tschirgi

Cephalad perfusion with Tyrode's solution of the spinal subarachnoid space between a lumbar and cisternal tap in anesthetized cats had no effect on spinal reflexes, respiration or pupillary size for periods of 8 hours. Alteration of Ca++ or K+ concentration in the perfusate produced immediate changes in these indices, indicating the availability of the perfusate to neural elements. The onset and course of patellar areflexia, respiratory depression and pupillary dilatation resulting from i.v. insulin-induced hypoglycemia could not be influenced by including high concentrations of glucose, glutamate, succinate or a combination of these latter two in the subarachnoid perfusate. It is concluded that the cerebrospinal fluid cannot act as a sufficient medium for transport from the blood of nutrient substrates essential for maintaining function in the central nervous system.


2018 ◽  
Vol 23 (1) ◽  
pp. 10-13
Author(s):  
James B. Talmage ◽  
Jay Blaisdell

Abstract Injuries that affect the central nervous system (CNS) can be catastrophic because they involve the brain or spinal cord, and determining the underlying clinical cause of impairment is essential in using the AMA Guides to the Evaluation of Permanent Impairment (AMA Guides), in part because the AMA Guides addresses neurological impairment in several chapters. Unlike the musculoskeletal chapters, Chapter 13, The Central and Peripheral Nervous System, does not use grades, grade modifiers, and a net adjustment formula; rather the chapter uses an approach that is similar to that in prior editions of the AMA Guides. The following steps can be used to perform a CNS rating: 1) evaluate all four major categories of cerebral impairment, and choose the one that is most severe; 2) rate the single most severe cerebral impairment of the four major categories; 3) rate all other impairments that are due to neurogenic problems; and 4) combine the rating of the single most severe category of cerebral impairment with the ratings of all other impairments. Because some neurological dysfunctions are rated elsewhere in the AMA Guides, Sixth Edition, the evaluator may consult Table 13-1 to verify the appropriate chapter to use.


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