Long survival of primary diffuse leptomeningeal gliomatosis following radiotherapy and temozolomide: case report and literature review
<p>Abstract</p> <p>Objective</p> <p>Primary diffuse leptomeningeal gliomatosis (PDLG) is a rare neoplasm with a short survival time of a few months. there is currently no standardized therapeutic approach for PDLG.</p> <p>Materials and methods</p> <...
| Main Authors: | , , , , , |
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| Format: | Article |
| Language: | English |
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BMC
2011-09-01
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| Series: | European Journal of Medical Research |
| Subjects: | |
| Online Access: | http://www.eurjmedres.com/content/16/9/415 |
| _version_ | 1828257249090338816 |
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| author | Hansen N Wittig A Hense J Kastrup O Gizewski ER Van de Nes JAP |
| author_facet | Hansen N Wittig A Hense J Kastrup O Gizewski ER Van de Nes JAP |
| author_sort | Hansen N |
| collection | DOAJ |
| description | <p>Abstract</p> <p>Objective</p> <p>Primary diffuse leptomeningeal gliomatosis (PDLG) is a rare neoplasm with a short survival time of a few months. there is currently no standardized therapeutic approach for PDLG.</p> <p>Materials and methods</p> <p>We report on a 53-year-old male patient who presented with epileptic seizures, gait disturbance, paraparesis and sensory deficits in the dermatomes T8-10.</p> <p>Results</p> <p>Magnetic resonance imaging (MRI) revealing numerous spinal and cranial gadolinium-enhancing nodules in the meninges and histopathology led us to diagnose primary diffuse leptomeningeal gliomatosis with WHO grade III astrocytic cells. Consecutively, the patient underwent craniospinal radiotherapy (30 Gy) and 11 sequential cycles of temozolomide. This regimen led to partial tumor regression. Thirteen months later, spinal MRI revealed tumor progression. Second-line chemotherapy with 5 cycles of irinotecan and bevacizumab did not prevent further clinical deterioration. The patient died twenty-two months after diagnosis, being the longest survival time described thus far with respect to PDLG consisting of astrocytic tumor cells.</p> <p>Conclusions</p> <p>Radiochemotherapy including temozolomide, as established standard therapy for brain malignant astrocytomas, might be valid as a basic therapeutic strategy for this PDLG subtype.</p> |
| first_indexed | 2024-04-13T02:38:55Z |
| format | Article |
| id | doaj.art-bcdb3c37a071478b8dada0054802fb04 |
| institution | Directory Open Access Journal |
| issn | 2047-783X |
| language | English |
| last_indexed | 2024-04-13T02:38:55Z |
| publishDate | 2011-09-01 |
| publisher | BMC |
| record_format | Article |
| series | European Journal of Medical Research |
| spelling | doaj.art-bcdb3c37a071478b8dada0054802fb042022-12-22T03:06:16ZengBMCEuropean Journal of Medical Research2047-783X2011-09-0116941510.1186/2047-783X-16-9-415Long survival of primary diffuse leptomeningeal gliomatosis following radiotherapy and temozolomide: case report and literature reviewHansen NWittig AHense JKastrup OGizewski ERVan de Nes JAP<p>Abstract</p> <p>Objective</p> <p>Primary diffuse leptomeningeal gliomatosis (PDLG) is a rare neoplasm with a short survival time of a few months. there is currently no standardized therapeutic approach for PDLG.</p> <p>Materials and methods</p> <p>We report on a 53-year-old male patient who presented with epileptic seizures, gait disturbance, paraparesis and sensory deficits in the dermatomes T8-10.</p> <p>Results</p> <p>Magnetic resonance imaging (MRI) revealing numerous spinal and cranial gadolinium-enhancing nodules in the meninges and histopathology led us to diagnose primary diffuse leptomeningeal gliomatosis with WHO grade III astrocytic cells. Consecutively, the patient underwent craniospinal radiotherapy (30 Gy) and 11 sequential cycles of temozolomide. This regimen led to partial tumor regression. Thirteen months later, spinal MRI revealed tumor progression. Second-line chemotherapy with 5 cycles of irinotecan and bevacizumab did not prevent further clinical deterioration. The patient died twenty-two months after diagnosis, being the longest survival time described thus far with respect to PDLG consisting of astrocytic tumor cells.</p> <p>Conclusions</p> <p>Radiochemotherapy including temozolomide, as established standard therapy for brain malignant astrocytomas, might be valid as a basic therapeutic strategy for this PDLG subtype.</p>http://www.eurjmedres.com/content/16/9/415primary diffuse leptomeningeal gliomatosistemozolomideradio-chemotherapy, malignant astrocytic cells, survival time |
| spellingShingle | Hansen N Wittig A Hense J Kastrup O Gizewski ER Van de Nes JAP Long survival of primary diffuse leptomeningeal gliomatosis following radiotherapy and temozolomide: case report and literature review European Journal of Medical Research primary diffuse leptomeningeal gliomatosis temozolomide radio-chemotherapy, malignant astrocytic cells, survival time |
| title | Long survival of primary diffuse leptomeningeal gliomatosis following radiotherapy and temozolomide: case report and literature review |
| title_full | Long survival of primary diffuse leptomeningeal gliomatosis following radiotherapy and temozolomide: case report and literature review |
| title_fullStr | Long survival of primary diffuse leptomeningeal gliomatosis following radiotherapy and temozolomide: case report and literature review |
| title_full_unstemmed | Long survival of primary diffuse leptomeningeal gliomatosis following radiotherapy and temozolomide: case report and literature review |
| title_short | Long survival of primary diffuse leptomeningeal gliomatosis following radiotherapy and temozolomide: case report and literature review |
| title_sort | long survival of primary diffuse leptomeningeal gliomatosis following radiotherapy and temozolomide case report and literature review |
| topic | primary diffuse leptomeningeal gliomatosis temozolomide radio-chemotherapy, malignant astrocytic cells, survival time |
| url | http://www.eurjmedres.com/content/16/9/415 |
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