Literature DB >> 1560255

Measurements of CSF biochemical tumor markers in patients with meningeal carcinomatosis and brain tumors.

H Nakagawa1, S Kubo, A Murasawa, S Nakajima, Y Nakajima, S Izumoto, T Hayakawa.   

Abstract

CSF beta-glucuronidase, polyamines and carcinoembryonic antigen (CEA) were analyzed in 16 patients with meningeal carcinomatosis from solid tumor in systemic organs, 27 with benign brain lesions, 18 with primary brain tumors, 14 with metastatic brain tumors and 5 with leptomeningeal dissemination of other malignant diseases. Beta-glucuronidase levels in all cases of meningeal carcinomatosis, meningeal gliomatosis and meningeal lymphoma were higher than 100 micrograms/dl/hr; on the other hand, levels in all cases of benign brain lesions were below 100 micrograms/dl/hr. Levels of beta-glucuronidase and polyamines were not high in the cases with positive cytology after tumor resection. Polyamine levels were below 0.05 nmol/ml in all cases after resection of the metastatic brain tumor. Cystic fluid of malignant tumors showed high levels of beta-glucuronidase and polyamines. On the other hand, the levels of polyamines in the cystic fluid of benign tumor were low, although the levels of beta-glucuronidase were high. Some cases of meningeal carcinomatosis with high levels of serum CEA did not show high levels of CSF CEA. For metastatic brain tumors, the cases with intraparenchymal tumors, especially with dural attachment showed high levels of beta-glucuronidase and CEA preoperatively, but they returned to normal after surgery. In cases of meningeal carcinomatosis treated by intrathecal chemotherapy with methotrexate (MTX) and cytosine arabinoside (Ara-C), CSF beta-glucuronidase reflected the neurological status better than the cell count decreased rapidly following chemotherapy and beta-glucuronidase was considered as a useful CSF marker in cases of meningeal carcinomatosis to monitor the course of the disease. The same situation was observed in CSF CEA and CEA was also considered as a useful marker when CEA levels in CSF are higher than those in serum.

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Year:  1992        PMID: 1560255     DOI: 10.1007/bf00172659

Source DB:  PubMed          Journal:  J Neurooncol        ISSN: 0167-594X            Impact factor:   4.130


  23 in total

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Journal:  J Neurosurg Sci       Date:  1982 Jul-Sep       Impact factor: 2.279

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Journal:  Cancer       Date:  1985-10-01       Impact factor: 6.860

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Journal:  Ann Neurol       Date:  1980-12       Impact factor: 10.422

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  5 in total

Review 1.  Meningeal metastases: clinical aspects and diagnosis.

Authors:  F Formaglio; A Caraceni
Journal:  Ital J Neurol Sci       Date:  1998-06

2.  Retrospective Analysis of Cerebrospinal Fluid Profiles in 228 Patients with Leptomeningeal Carcinomatosis : Differences According to the Sampling Site, Symptoms, and Systemic Factors.

Authors:  Youngbo Shim; Ho-Shin Gwak; Sohee Kim; Jungnam Joo; Sang-Hoon Shin; Heon Yoo
Journal:  J Korean Neurosurg Soc       Date:  2016-10-24

3.  Cerebrospinal fluid metabolomic profiles can discriminate patients with leptomeningeal carcinomatosis from patients at high risk for leptomeningeal metastasis.

Authors:  Byong Chul Yoo; Jun Hwa Lee; Kyung-Hee Kim; Weiwei Lin; Jong Heon Kim; Jong Bae Park; Hyun Jin Park; Sang Hoon Shin; Heon Yoo; Ji Woong Kwon; Ho-Shin Gwak
Journal:  Oncotarget       Date:  2017-09-18

4.  Diagnostic Value of CYFRA 21-1 in the Cerebrospinal Fluid for Leptomeningeal Metastasis.

Authors:  Zhen Zhang; Chenglin Tian; Qiang Shi; Jing Hao; Na Zhao; Zhijie Liu
Journal:  Dis Markers       Date:  2017-02-19       Impact factor: 3.434

Review 5.  Leptomeningeal disease: current diagnostic and therapeutic strategies.

Authors:  Gautam Nayar; Tiffany Ejikeme; Pakawat Chongsathidkiet; Aladine A Elsamadicy; Kimberly L Blackwell; Jeffrey M Clarke; Shivanand P Lad; Peter E Fecci
Journal:  Oncotarget       Date:  2017-08-16
  5 in total

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