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Keywords central nervous system germ ce...

central nervous system germ cell tumors

https://read.qxmd.com/read/37559808/diffuse-leptomeningeal-glioneuronal-tumor-with-fgfr1-mutation-in-a-29-year-old-male
#21
Minsu Kim, Ki Rim Lee, Gheeyoung Choe, Kihwan Hwang, Jae Hyoung Kim
This study reports on diffuse leptomeningeal glioneuronal tumor (DL-GNT) in a 29-year-old male. DL-GNT is a rare central nervous system (CNS) tumor mostly seen in children and only few cases have been reported in adult patients. Our patient presented with a chronic headache that lasted for five months. MR imaging showed mild hydrocephalus, multiple rim-enhancing nodular lesions in the suprasellar cistern, diffuse leptomeningeal enhancement in the lumbosacral area, and multiple small non-enhancing cyst-appearing lesions not suppressed on fluid attenuated inversion recovery (FLAIR) images in the bilateral basal ganglia, thalami, and cerebral hemispheres...
July 2023: J Korean Soc Radiol
https://read.qxmd.com/read/37534382/children-s-oncology-group-s-2023-blueprint-for-research-central-nervous-system-tumors
#22
JOURNAL ARTICLE
Sarah E S Leary, Arzu Onar-Thomas, Jason Fangusaro, Nicholas G Gottardo, Kenneth Cohen, Amy Smith, Annie Huang, Daphne Haas-Kogan, Maryam Fouladi
Tumors of the central nervous system (CNS) are a leading cause of morbidity and mortality in the pediatric population. Molecular characterization in the last decade has redefined CNS tumor diagnoses and risk stratification; confirmed the unique biology of pediatric tumors as distinct entities from tumors that occur in adulthood; and led to the first novel targeted therapies receiving Food and Drug Administration (FDA) approval for children with CNS tumors. There remain significant challenges to overcome: children with unresectable low-grade glioma may require multiple prolonged courses of therapy affecting quality of life; children with high-grade glioma have a dismal long-term prognosis; children with medulloblastoma may suffer significant short- and long-term morbidity from multimodal cytotoxic therapy, and approaches to improve survival in ependymoma remain elusive...
September 2023: Pediatric Blood & Cancer
https://read.qxmd.com/read/37519792/pediatric-diencephalic-tumors-a-constellation-of-entities-and-management-modalities
#23
REVIEW
Soniya N Pinto, Jason Chiang, Ibrahim Qaddoumi, David Livingston, Asim Bag
The diencephalon is a complex midline structure consisting of the hypothalamus, neurohypophysis, subthalamus, thalamus, epithalamus, and pineal body. Tumors arising from each of these diencephalic components differ significantly in terms of biology and prognosis. The aim of this comprehensive review is to describe the epidemiology, clinical symptoms, imaging, histology, and molecular markers in the context of the 2021 WHO classification of central nervous system neoplasms . We will also discuss the current management of each of these tumors...
2023: Frontiers in Oncology
https://read.qxmd.com/read/37501569/the-role-of-neoadjuvant-chemotherapy-in-the-management-of-metastatic-central-nervous-system-germinoma-a-meta-analysis
#24
JOURNAL ARTICLE
Mohammad H Abu-Arja, Margaret S Shatara, M Fatih Okcu, Susan L McGovern, Jack M Su, Mohamed S Abdelbaki
BACKGROUND: The role of neoadjuvant chemotherapy in treating patients with metastatic central nervous system (CNS) germinoma is controversial. METHODS: We compared the relapse-free survival (RFS) of different treatment modalities by performing a meta-analysis using published data. We summarized all data using standard descriptive statistics. We used the Kaplan-Meier method to estimate RFS and their corresponding 95% confidence intervals (CIs). We used the log-rank test for the comparison of survival functions...
October 2023: Pediatric Blood & Cancer
https://read.qxmd.com/read/37452948/brain-and-spinal-tumors-originating-from-the-germ-line-cells
#25
JOURNAL ARTICLE
Tai-Tong Wong, Min-Lan Tsai, Hsi Chang, Kevin Li-Chun Hsieh, Donald Ming-Tak Ho, Shih-Chieh Lin, Hsiu-Ju Yen, Yi-Wei Chen, Hsin-Lun Lee, Tsui-Fen Yang
Primary central nervous system germ cell tumors (CNS GCTs) are part of the GCTs in children and adults. This tumor entity presents with geographic variation, age, and sex predilection. There are two age peaks of incidence distribution at the first few months of life and in adolescence. CNS GCTs are heterogeneous in histopathological subtypes, locations, and tumor marker (AFP, β-hCG) secretions. In the WHO CNS tumor classification, GCTS are classified as germinoma and nongerminomatous GCT (NGGCT) with different subtypes (including teratoma)...
2023: Advances in Experimental Medicine and Biology
https://read.qxmd.com/read/37452862/pediatric-paravertebral-tumors-analysis-of-96-patients
#26
JOURNAL ARTICLE
Deniz Kizmazoglu, Dilek Ince, Emre Cecen, Ceren Kizmazoglu, Handan Guleryuz, Erdener Ozer, Ayse Demiral, Nur Olgun
PURPOSE: The most important complication of paravertebral tumors is cord compression (CC), which is an oncologic emergency. Early and appropriate intervention is important in terms of reducing morbidity and mortality. Here, we report our clinical experience with paravertebral tumors. METHODS: The files of patients who were followed up for benign/malignant paravertebral tumors between 1988 and 2022 were evaluated retrospectively. RESULTS: There were 96 patients with paravertebral tumors...
July 15, 2023: Child's Nervous System: ChNS: Official Journal of the International Society for Pediatric Neurosurgery
https://read.qxmd.com/read/37405483/-diagnosis-of-germ-cell-tumors
#27
REVIEW
Armin Bachhuber
CLINICAL/METHODICAL ISSUE: Intracranial germ cell tumors are rare central nervous system (CNS) diseases in Europa and America. Because of their low frequency and lack of typical imaging features, they represent a difficult diagnosis for any radiologist. STANDARD RADIOLOGICAL METHODS: Magnetic resonance imaging (MRI) is a sensible diagnostic tool for the initial diagnosis of germ cell tumors, although it has limitations. METHODOLOGICAL INNOVATIONS: So far, no typical morphologic pattern as a red flag for germ cell tumors has been identified...
July 5, 2023: Radiologie (Heidelb)
https://read.qxmd.com/read/37179159/hypertrophic-pachymeningitis-due-to-igg4-related-disease-rd-igg4-a-case-report
#28
JOURNAL ARTICLE
Paira Sergio, Reibaldi Alejandro, Froullet Cristian
INTRODUCTION: Hypertrophic pachymeningitis (HP) is a clinico-radiological entity characterized by a thickening of the dura mater that may be focal or diffuse and manifested by a variety of neurological syndromes. Aetiologically, it is classified as infectious, neoplastic, autoimmune, and idiopathic. Many of these formerly idiopathic cases have been shown to fall into the spectrum of IgG4-related disease. OBJECTIVE: To describe the case of a patient attended for neurological involvement due to hypertrophic pachymeningitis with initial diagnosis of inflammatory myofibroblastic tumour and final diagnosis of IgG4-related disease...
2023: Reumatología clinica
https://read.qxmd.com/read/37101365/maternal-migraine-and-risk-of-pediatric-cancers
#29
JOURNAL ARTICLE
Helen T Orimoloye, Julia E Heck, Andrew Charles, Chai Saechao, Di He, Noah Federman, Jorn Olsen, Beate Ritz, Johnni Hansen
BACKGROUND: Maternal migraine has been linked to adverse birth outcomes including low birth weight and preterm birth, as well as congenital anomalies in offspring. It has been speculated that this may be due to the use of medications in pregnancy, but lifestyle, genetic, hormonal, and neurochemical factors could also play a role. There is evidence for varying cancer incidences among adults with migraine. Here, we utilized data from national registries in Denmark to examine associations between maternal diagnoses of migraine and risk for cancer in offspring...
July 2023: Pediatric Blood & Cancer
https://read.qxmd.com/read/37046379/diffuse-pediatric-type-high-grade-glioma-arising-in-an-ovarian-mature-cystic-teratoma
#30
JOURNAL ARTICLE
Lena Elmuti, Julia Amundson, Elise Oberman, Aarti Kamat, Laura Sedig, Ricardo R Lastra, Kenneth Aldape, Martha Quezado, Drew W Pratt, Patrick J Cimino, Zied Abdullaev, Peter Pytel, Mark A Applebaum, Jennifer A Bennett
Immature neuroectodermal tissue can be found in the ovary as part of an immature teratoma or as part of a teratoma with malignant neuroectodermal transformation. Such lesions may closely resemble central nervous system tumors, but their biologic similarity is unclear. We describe an 18-yr-old female who presented with abdominal pain caused by an ovarian mass with widespread metastases. Histology showed a primitive, high-grade tumor arising in the background of a mature teratoma. The tumor was SOX10 positive, with focal expression of GFAP, S100, NSE, and synaptophysin...
April 13, 2023: International Journal of Gynecological Pathology
https://read.qxmd.com/read/36937498/occult-germinoma-of-the-intramedullary-spinal-cord-a-case-report
#31
Takumi Hoshimaru, Fugen Takagi, Yuichiro Tsuji, Ryokichi Yagi, Ryo Hiramatsu, Masahiro Kameda, Naosuke Nonoguchi, Motomasa Furuse, Shinji Kawabata, Toshihiro Takami, Masahiko Wanibuchi
Primary germ cell tumors of the central nervous system (CNS) typically occur in the neurohypophysis, hypothalamus, or pineal gland and rarely in the spinal cord. We report a case of a spinal intramedullary tumor, which was first detected on magnetic resonance imaging (MRI) 41 months after the initial symptoms, with a verified pathological diagnosis of germinoma. The initial symptom was an abnormal sensation in the left plantar region that gradually worsened, resulting in severe sensory disturbance, difficulty in standing, and even bladder rectal disturbance...
2023: NMC Case Report Journal
https://read.qxmd.com/read/36863221/primary-midbrain-germinomas-report-of-a-rare-case-with-an-updated-review-of-the-literature
#32
REVIEW
Abdullah Keles, Halli T Olsen, Alex F Nisbet, Jeffrey Helgager, Mustafa K Baskaya
Intracranial germinomas are most commonly extra-axial germ cell tumors that are predominantly found in the pineal and suprasellar regions. Primary intra-axial midbrain germinomas are extremely rare, with only eight reported cases. Here we present a 30-year-old man who presented with severe neurological deficits, with an MRI that showed a heterogeneously enhancing mass with ill-defined margins in the midbrain, and with surrounding vasogenic edema extending to the thalamus. The presumptive preoperative differential diagnosis included glial tumors and lymphoma...
April 2023: Clinical Neurology and Neurosurgery
https://read.qxmd.com/read/36811535/malignant-tumors-in-pediatric-population-of-ukraine-trends-and-structural-features
#33
JOURNAL ARTICLE
A F Shipko, Z P Fedorenko, A Yu Ryzhov
UNLABELLED: The creation of a central bank of personalized information of cancer patients, including children, allowed to obtain objective data and establish continuous cancer surveillance in the child population in Ukraine. The aim of the study was to analyze the dynamics of cancer incidence (1989-2019) and mortality (1999-2019) based on the 3rd revision of International Classification of Childhood Cancer (ICCC-3). MATERIALS AND METHODS: A study cohort includes 31,537 patients aged 0-19 years at the time of diagnosis in 1989-2019, registered in Ukrainian population...
December 2022: Experimental Oncology
https://read.qxmd.com/read/36776860/generation-of-mesenchymal-stromal-cells-from-urine-derived-ipscs-of-pediatric-brain-tumor-patients
#34
JOURNAL ARTICLE
Carmen Baliña-Sánchez, Yolanda Aguilera, Norma Adán, Jesús María Sierra-Párraga, Laura Olmedo-Moreno, Concepción Panadero-Morón, Rosa Cabello-Laureano, Catalina Márquez-Vega, Alejandro Martín-Montalvo, Vivian Capilla-González
Human induced pluripotent stem cells (iPSCs) provide a virtually inexhaustible source of starting material for next generation cell therapies, offering new opportunities for regenerative medicine. Among different cell sources for the generation of iPSCs, urine cells are clinically relevant since these cells can be repeatedly obtained by non-invasive methods from patients of any age and health condition. These attributes encourage patients to participate in preclinical and clinical research. In particular, the use of urine-derived iPSC products is a convenient strategy for children with brain tumors, which are medically fragile patients...
2023: Frontiers in Immunology
https://read.qxmd.com/read/36708005/childhood-cancer-and-hematological-disorders-negatively-affect-spermatogonial-quantity-at-diagnosis-a-retrospective-study-of-a-male-fertility-preservation-cohort
#35
JOURNAL ARTICLE
Ieva Masliukaite, Elissavet Ntemou, Elizabeth A M Feijen, Marianne van de Wetering, Andreas Meissner, Alexandre T Soufan, Sjoerd Repping, Leontien M C Kremer, Kirsi Jahnukainen, Ellen Goossens, Ans M M van Pelt
STUDY QUESTION: What is the impact of cancer or hematological disorders on germ cells in pediatric male patients? SUMMARY ANSWER: Spermatogonial quantity is reduced in testes of prepubertal boys diagnosed with cancer or severe hematological disorder compared to healthy controls and this reduction is disease and age dependent: patients with central nervous system cancer (CNS tumors) and hematological disorders, as well as boys <7 years are the most affected...
January 27, 2023: Human Reproduction
https://read.qxmd.com/read/36521378/primary-central-nervous-system-germ-cell-tumors-in-children-and-young-adults-a-review-of-controversies-in-diagnostic-and-treatment-approach
#36
JOURNAL ARTICLE
Kee Kiat Yeo, Sumanth Nagabushan, Girish Dhall, Mohamed S Abdelbaki
Primary central nervous system (CNS) germ cell tumors (GCT) are a rare heterogenous group of cancers, arising most commonly in the second decade of life. Through several clinical trials conducted around the world by various groups, the treatment approach for CNS GCT has advanced substantially with generally improved overall outcomes. In recent years, the goal of clinical trials has been focused on reduction of the radiotherapy burden and minimization of long-term toxicity. This review summarizes the current diagnostic and treatment regimens for CNS GCT, examines the controversies associated with these approaches, gaps in contemporary knowledge, and underscores the challenges we face...
December 13, 2022: Neoplasia: An International Journal for Oncology Research
https://read.qxmd.com/read/36509072/pediatric-central-nervous-system-cancers-version-2-2023-nccn-clinical-practice-guidelines-in-oncology
#37
JOURNAL ARTICLE
Amar Gajjar, Anita Mahajan, Mohamed Abdelbaki, Clarke Anderson, Reuben Antony, Tejus Bale, Ranjit Bindra, Daniel C Bowers, Kenneth Cohen, Bonnie Cole, Kathleen Dorris, Ralph Ermoian, Andrea Franson, Jeffrey Helgager, Daniel Landi, Chi Lin, Laura Metrock, Ronica Nanda, Joshua Palmer, Sonia Partap, Ashley Plant, Sumit Pruthi, Renee Reynolds, Paul Ruggieri, Duncan Stearns, Phillip Storm, Anthony Wang, Katherine Warren, Nicholas Whipple, Wafik Zaky, Nicole R McMillian, Lenora A Pluchino
Central nervous system (CNS) cancers account for approximately one quarter of all pediatric tumors and are the leading cause of cancer-related death in children. More than 4,000 brain and CNS tumors are diagnosed each year in children and teens, and the incidence rate has remained stagnant in recent years. The most common malignant pediatric CNS tumors are gliomas, embryonal tumors consisting of predominately medulloblastomas, and germ cell tumors. The inaugural version of the NCCN Guidelines for Pediatric Central Nervous System Cancers focuses on the diagnosis and management of patients with pediatric diffuse high-grade gliomas...
December 2022: Journal of the National Comprehensive Cancer Network: JNCCN
https://read.qxmd.com/read/36443673/endoscopic-aqueductal-membrane-fenestration-was-effective-for-intractable-hydrocephalus-after-removal-of-a-nongerminomatous-germ-cell-tumor-exhibiting-growing-teratoma-syndrome-a-case-report
#38
JOURNAL ARTICLE
Sosho Kajiwara, Hideo Nakamura, Kiyohiko Sakata, Satoru Komaki, Tetsuya Negoto, Motohiro Morioka
BACKGROUND: Primary central nervous system (CNS) germ cell tumors (GCTs) are rare neoplasms predominantly observed in the pediatric and young adult populations. A mixed GCT including immature teratoma exhibiting growing teratoma syndrome is presented. The pathogenesis of growing teratoma syndrome remains unclear, and its treatment strategy has not been established. GCTs are often located within the ventricles, causing hydrocephalus, which sometimes improves after removal of the tumor due to restoration of cerebrospinal fluid (CSF) flow...
November 28, 2022: BMC Pediatrics
https://read.qxmd.com/read/36307659/all-pineal-tumors-expressing-germ-cell-tumor-markers-are-not-necessarily-germ-cell-tumors-histopathological-and-molecular-study-of-a-midline-primary-intracranial-sarcoma-dicer1-mutant
#39
JOURNAL ARTICLE
Thibaut Wolf, Andres Hugo Coca, Noelle Weingertner, Marie Pierre Chenard, Alexandra Meurgey, Damien Reita, Erwan Pencreach, Pascale Varlet, Natacha Entz-Werlé, Benoît Lhermitte
Primary intracranial sarcoma DICER1-mutant is a rare and newly recognized tumor type introduced in the 2021 WHO Classification of Central Nervous System Tumors. It is defined as a spindle cell sarcoma dysplaying eosinophilic intracytoplasmic globules, myogenic differentiation, and DICER1 gene mutation, either somatic or germline. Most reported cases were hemispheric except one, recently described in the pineal region. Here, we report the case of a 12 year-old boy with a pineally located tumor. Despite midline location, poorly differenciated morphology and germ cell marker expression, the association of DICER1 and NF1 hotspot mutations and a specific DNA methylation signature finally lead to the diagnosis of primary intracranial sarcoma DICER1-mutant instead of germ cell tumor...
October 28, 2022: Virchows Archiv: An International Journal of Pathology
https://read.qxmd.com/read/36271932/intracranial-germinoma-in-the-lateral-ventricle-with-polydipsia-and-polyuria-a-case-report-and-literature-review
#40
JOURNAL ARTICLE
Yuki Kuranari, Tomoru Miwa, Maya Kono, Hironori Shibata, Tomohiro Ishii, Tomonobu Hasegawa
Central nervous system germ cell tumors (CNSGCTs) are rare neoplasms which usually develop in the midline structures. They are occasionally involved in off-midline structures of the brain. Here, we report an extremely rare case of an intracranial germinoma in the lateral ventricle. The patient was a 10-year-old boy with a 1-year history of polydipsia and polyuria. Brain magnetic resonance imaging (MRI) showed a relatively homogeneously enhancing lesion in the lateral ventricle, and the posterior pituitary gland was not hyperintense on T1-weighted imaging...
October 22, 2022: Child's Nervous System: ChNS: Official Journal of the International Society for Pediatric Neurosurgery
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