{"title":"一例独特现象:多形性胶质母细胞瘤脑脊膜扩散。","authors":"Kanza Farhan, Yumna Ahmed, Fatima Shaukat","doi":"10.47391/JPMA.20698","DOIUrl":null,"url":null,"abstract":"<p><p>Leptomeningeal spread (LMS) of glioblastoma multiforme (GBM) is a rare event, presenting challenges in both diagnosis and treatment. Here, we describe the case of a 59-year-old GBM patient who experienced LMS during his treatment. Despite multimodal therapy, including surgery, chemotherapy, and radiotherapy, the patient's condition rapidly deteriorated. The case illustrates the difficulty in treating GBM and the restricted ability of available therapies to stop LMS. This manifestation is uncommon, which highlights the need for increased awareness, ongoing study, and development of tailored treatments. Key factors influencing LMS include tumour size, age, and anatomical location. Diagnostic challenges arise due to the rarity of LMS in GBM and its atypical presentation. Therapeutic interventions targeting LMS are lacking, with poor prognosis and low survival rates. To improve patient outcomes, more studies should be done on creating efficient treatment regimens and figuring out the markers associated with LMS development in GBM.</p>","PeriodicalId":54369,"journal":{"name":"Journal of the Pakistan Medical Association","volume":"75 4","pages":"683-686"},"PeriodicalIF":0.8000,"publicationDate":"2025-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Case report of a unique phenomenon: leptomeningeal spread in glioblastoma multiforme.\",\"authors\":\"Kanza Farhan, Yumna Ahmed, Fatima Shaukat\",\"doi\":\"10.47391/JPMA.20698\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Leptomeningeal spread (LMS) of glioblastoma multiforme (GBM) is a rare event, presenting challenges in both diagnosis and treatment. Here, we describe the case of a 59-year-old GBM patient who experienced LMS during his treatment. Despite multimodal therapy, including surgery, chemotherapy, and radiotherapy, the patient's condition rapidly deteriorated. The case illustrates the difficulty in treating GBM and the restricted ability of available therapies to stop LMS. This manifestation is uncommon, which highlights the need for increased awareness, ongoing study, and development of tailored treatments. Key factors influencing LMS include tumour size, age, and anatomical location. Diagnostic challenges arise due to the rarity of LMS in GBM and its atypical presentation. Therapeutic interventions targeting LMS are lacking, with poor prognosis and low survival rates. To improve patient outcomes, more studies should be done on creating efficient treatment regimens and figuring out the markers associated with LMS development in GBM.</p>\",\"PeriodicalId\":54369,\"journal\":{\"name\":\"Journal of the Pakistan Medical Association\",\"volume\":\"75 4\",\"pages\":\"683-686\"},\"PeriodicalIF\":0.8000,\"publicationDate\":\"2025-04-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of the Pakistan Medical Association\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.47391/JPMA.20698\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"MEDICINE, GENERAL & INTERNAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of the Pakistan Medical Association","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.47391/JPMA.20698","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"MEDICINE, GENERAL & INTERNAL","Score":null,"Total":0}
Case report of a unique phenomenon: leptomeningeal spread in glioblastoma multiforme.
Leptomeningeal spread (LMS) of glioblastoma multiforme (GBM) is a rare event, presenting challenges in both diagnosis and treatment. Here, we describe the case of a 59-year-old GBM patient who experienced LMS during his treatment. Despite multimodal therapy, including surgery, chemotherapy, and radiotherapy, the patient's condition rapidly deteriorated. The case illustrates the difficulty in treating GBM and the restricted ability of available therapies to stop LMS. This manifestation is uncommon, which highlights the need for increased awareness, ongoing study, and development of tailored treatments. Key factors influencing LMS include tumour size, age, and anatomical location. Diagnostic challenges arise due to the rarity of LMS in GBM and its atypical presentation. Therapeutic interventions targeting LMS are lacking, with poor prognosis and low survival rates. To improve patient outcomes, more studies should be done on creating efficient treatment regimens and figuring out the markers associated with LMS development in GBM.
期刊介绍:
Primarily being a medical journal, JPMA publishes scholarly research focusing on the various fields in the areas of health and medical education. It publishes original research describing recent advances in health particularly clinical studies, clinical trials, assessments of pathogens of diagnostic importance, medical genetics and epidemiological studies. Review articles highlighting importance of various issues in the domain of public health, drug research and medical education are also accepted. As a leading journal of South Asia, JPMA remains cognizant of the recent advances in the rapidly growing fields of biomedical sciences, it invites and encourages scholars to write short reviews and invited editorials on the emerging issues. We particularly aim to promote health standards of developing countries by encouraging manuscript submissions on issues affecting the public health and health delivery services.