Skip to main content Accessibility help
×
Hostname: page-component-76fb5796d-9pm4c Total loading time: 0 Render date: 2024-04-29T02:49:07.499Z Has data issue: false hasContentIssue false

8 - Cytopathology of Cerebrospinal Fluid

Published online by Cambridge University Press:  04 August 2010

Hannes Vogel
Affiliation:
Stanford University School of Medicine, California
Get access

Summary

CLINICAL INDICATIONS

Examination of cerebrospinal fluid (CSF) specimens is a routine component of most neurological evaluations and includes cell count, biochemical analysis, and cytological examination. Samples may be obtained by lumbar puncture or from the lateral ventricles or cisterna magna either at the time of surgery or from indwelling ventricular shunts. CSF analysis is not only useful for diagnosis of new neoplastic processes, but is routinely used for monitoring the efficacy of central nervous system (CNS) chemotherapy such as recurrence of lymphoma or leukemia and or in the evaluation of infections in immunocompromised patients. As with other aspects of cytology, the cytological findings must be correlated with the clinical, biochemical, and radiographic findings to ensure diagnostic accuracy.

SPECIMEN PREPARATION (CYTOPREPARATION)

CSF specimens are unique in cytology with respect to the small sample size, lack of cellular abundance, and susceptibility of the sample to undergo rapid degeneration. With this in mind, processing of CSF specimens for cell count, biochemical analysis, cytological preparation, and additional tests such as flow cytometric analysis in cases of suspected hematopoietic malignancies should be done as soon as possible. The specimen is collected in plastic tubes and divided among several divisions within the laboratory for specific testing Cytological diagnosis should be performed from the third or last tube since it will have less blood contamination in cases of traumatic tap.

The most common stain employed in CSF cytology is the Wright–Giemsa preparation, which is most useful for classification of hematopoietic cells and cytoplasmic detail while the Papanicolaou stain, best for nuclear detail, is the standard used for filter and cytocentrifugation preparations.

Type
Chapter
Information
Nervous System , pp. 477 - 492
Publisher: Cambridge University Press
Print publication year: 2009

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

Save book to Kindle

To save this book to your Kindle, first ensure coreplatform@cambridge.org is added to your Approved Personal Document E-mail List under your Personal Document Settings on the Manage Your Content and Devices page of your Amazon account. Then enter the ‘name’ part of your Kindle email address below. Find out more about saving to your Kindle.

Note you can select to save to either the @free.kindle.com or @kindle.com variations. ‘@free.kindle.com’ emails are free but can only be saved to your device when it is connected to wi-fi. ‘@kindle.com’ emails can be delivered even when you are not connected to wi-fi, but note that service fees apply.

Find out more about the Kindle Personal Document Service.

Available formats
×

Save book to Dropbox

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Dropbox.

Available formats
×

Save book to Google Drive

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Google Drive.

Available formats
×