{"title":"Germinoma in late adulthood with extensive dissemination: a case report and literature review.","authors":"Rindai Saito, Yosuke Kitagawa, Hirokazu Takami, Kento Mitani, Takashi Aoka, Mariko Tanaka, Masashi Nomura, Nobuhito Saito","doi":"10.1007/s10014-026-00551-5","DOIUrl":null,"url":null,"abstract":"<p><p>Central nervous system germ cell tumors (CNS GCTs) are exceptionally rare in patients aged 60 years or older. We report a 61-year-old man with progressive weight loss and endocrine dysfunction over 20 months, in whom magnetic resonance imaging revealed enhancing lesions including the suprasellar and sellar regions, optic tracts, ventricular walls, corpus callosum, and dorsal medulla. Biopsy findings supported a diagnosis of germinoma in the sampled tissue, and DNA methylation profiling demonstrated a molecular profile consistent with conventional germinoma. The patient underwent whole ventricular irradiation and carboplatin-etoposide chemotherapy. Febrile neutropenia during the first cycle required subsequent etoposide dose reductions, but he achieved marked radiographic regression. A descriptive review identified five cases, including the present case, for which sufficient individual clinicopathological information was available. This case highlights that CNS GCTs in older adults may radiologically mimic primary CNS lymphoma and that integrated pathological assessment, including morphology and immunohistochemistry, is essential for diagnosis. In this diagnostically challenging presentation, DNA methylation profiling provided complementary molecular support for the histopathological diagnosis of conventional germinoma.</p>","PeriodicalId":9226,"journal":{"name":"Brain Tumor Pathology","volume":" ","pages":""},"PeriodicalIF":2.2000,"publicationDate":"2026-10-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Brain Tumor Pathology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1007/s10014-026-00551-5","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CLINICAL NEUROLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Central nervous system germ cell tumors (CNS GCTs) are exceptionally rare in patients aged 60 years or older. We report a 61-year-old man with progressive weight loss and endocrine dysfunction over 20 months, in whom magnetic resonance imaging revealed enhancing lesions including the suprasellar and sellar regions, optic tracts, ventricular walls, corpus callosum, and dorsal medulla. Biopsy findings supported a diagnosis of germinoma in the sampled tissue, and DNA methylation profiling demonstrated a molecular profile consistent with conventional germinoma. The patient underwent whole ventricular irradiation and carboplatin-etoposide chemotherapy. Febrile neutropenia during the first cycle required subsequent etoposide dose reductions, but he achieved marked radiographic regression. A descriptive review identified five cases, including the present case, for which sufficient individual clinicopathological information was available. This case highlights that CNS GCTs in older adults may radiologically mimic primary CNS lymphoma and that integrated pathological assessment, including morphology and immunohistochemistry, is essential for diagnosis. In this diagnostically challenging presentation, DNA methylation profiling provided complementary molecular support for the histopathological diagnosis of conventional germinoma.
期刊介绍:
Brain Tumor Pathology is the official journal of the Japan Society of Brain Tumor Pathology. This international journal documents the latest research and topical debate in all clinical and experimental fields relating to brain tumors, especially brain tumor pathology. The journal has been published since 1983 and has been recognized worldwide as a unique journal of high quality. The journal welcomes the submission of manuscripts from any country. Membership in the society is not a prerequisite for submission. The journal publishes original articles, case reports, rapid short communications, instructional lectures, review articles, letters to the editor, and topics.Review articles and Topics may be recommended at the annual meeting of the Japan Society of Brain Tumor Pathology. All contributions should be aimed at promoting international scientific collaboration.