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Letters |
a Address correspondence to this author at: Department of Clinical Chemistry (CKCL 564), University Hospital Nijmegen, P.O. Box 9101, 6500 HB Nijmegen, The Netherlands. Fax 31-243541743; e-mail D.Swinkels@CKCL.azn.nl.
Departments of
1
Clinical Chemistry,,
2
Pathology, and
3
Neurology, University Hospital Nijmegen, P.O. Box 9101, 6500 HB Nijmegen, The Netherlands
To the Editor:
Leptomeningeal metastasis (LMM) occurs in 38% of all cancer patients. Of the solid tumors, breast cancer, lung cancer, and malignant melanoma are the most common to metastasize to the leptomeninges (1). The prognosis for patients with LMM is poor: most individuals survive a median of only ~4 months. Early diagnosis may improve the clinical response to radiotherapy and (intrathecal) chemotherapy, and may lead to more effective palliation and prolonged survival (1).
Traditionally, a definitive diagnosis of LMM requires cytological detection of malignant cells in the cerebrospinal fluid (CSF). Interpretation is often aided by immunocytochemical techniques. Unfortunately, these CSF samples often contain very few morphologically identifiable malignant cells. In these cases, no definitive diagnosis can be established, leading to "suspicious" or "atypical" diagnoses (1).
Molecular detection of tumor-derived DNA in CSF can potentially improve
early and sensitive detection of LMM because no intact cells are
required for diagnosis (2)(3).
References
The following articles in journals at HighWire Press have cited this article:
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J. B. de Kok, T. J.M. Ruers, G. N.P. van Muijen, A. van Bokhoven, H. L. Willems, and D. W. Swinkels Real-Time Quantification of Human Telomerase Reverse Transcriptase mRNA in Tumors and Healthy Tissues Clin. Chem., March 1, 2000; 46(3): 313 - 318. [Abstract] [Full Text] [PDF] |
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