{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,5,2]],"date-time":"2025-05-02T16:48:06Z","timestamp":1746204486563},"reference-count":15,"publisher":"Scientific Scholar","content-domain":{"domain":["surgicalneurologyint.com"],"crossmark-restriction":true},"short-container-title":[],"abstract":"<jats:sec id=\"st1\">\n<jats:title>Background: <\/jats:title>\n<jats:p>Intravascular large B-cell lymphoma (IVLBCL) is a rare entity among large B-cell non-Hodgkin lymphomas and is often difficult to diagnose. We report the case of a patient with IVLBCL who presented with central nervous system (CNS) symptoms alone, in which positron emission tomography (PET) enabled a rapid and accurate diagnosis.<\/jats:p>\n<\/jats:sec>\n<jats:sec id=\"st2\">\n<jats:title>Case Description: <\/jats:title>\n<jats:p>An 81-year-old woman was admitted to our hospital with a 3-month history of gradually progressive dementia and declining spontaneity. Magnetic resonance imaging revealed multiple hyperintense lesions bilaterally on diffusion-weighted imaging without enhancement on gadolinium-enhanced T1-weighted imaging. Laboratory findings showed elevated serum lactate dehydrogenase (626 U\/L) and soluble interleukin-2 receptor (sIL-2R) (4692 U\/mL). Cerebrospinal fluid (CSF) analysis showed slightly elevated levels of protein (166 mg\/dL) and lymphocytic cells (29\/\u03bcL), and \u03b22-microglobulin (\u03b22-MG) (4.6 mg\/L) was highly elevated. Whole-body computed tomography revealed faint ground-glass opacities in the upper and middle lung fields and diffuse enlargement of both kidneys without lymph node swelling. <jats:sup>18<\/jats:sup>F-fluorodeoxyglucose (FDG)-PET showed diffuse and remarkably high FDG uptake in both upper lungs and kidneys without uptake by lymph nodes, suggesting a malignant hematological disease. IVLBCL was confirmed histologically by incisional random skin biopsy from the abdomen. Chemotherapy using R-CHOP regimen in combination with intrathecal methotrexate injection was started on day 5 after admission and follow-up neuroimaging showed no signs of recurrence.<\/jats:p>\n<\/jats:sec>\n<jats:sec id=\"st3\">\n<jats:title>Conclusion: <\/jats:title>\n<jats:p>IVLBCL presenting with CNS symptoms alone is rare and often has a poor prognosis associated with delayed diagnosis, and various evaluations (including systemic analysis) are therefore necessary for early diagnosis. FDG-PET, in addition to identification of clinical symptoms and evaluation of serum sIL-2R and CSF \u03b22-MG, enables rapid therapeutic intervention in IVLBCL presenting with CNS symptoms.<\/jats:p>\n<\/jats:sec>","DOI":"10.25259\/sni_1175_2022","type":"journal-article","created":{"date-parts":[[2023,3,17]],"date-time":"2023-03-17T08:24:00Z","timestamp":1679041440000},"page":"89","update-policy":"http:\/\/dx.doi.org\/10.25259\/crossmark_policy","source":"Crossref","is-referenced-by-count":1,"title":["Clinical utility of positron emission tomography leading to rapid and accurate diagnosis of intravascular large B-cell lymphoma presenting with the central nervous system symptoms alone: A case report and review of the literature"],"prefix":"10.25259","volume":"14","author":[{"given":"Ryo","family":"Inagaki","sequence":"first","affiliation":[{"name":"Department of Neurosurgery, Ehime University School of Medicine, Toon, Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Akihiro","family":"Inoue","sequence":"additional","affiliation":[{"name":"Department of Neurosurgery, Ehime University School of Medicine, Toon, Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Yukihiro","family":"Miyazaki","sequence":"additional","affiliation":[{"name":"Department of Hematology, Clinical Immunology and Infectious Diseases, Ehime University School of Medicine, Toon, Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Kota","family":"Kanehisa","sequence":"additional","affiliation":[{"name":"Department of Neurosurgery, Ehime University School of Medicine, Toon, Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Joji","family":"Kunihiro","sequence":"additional","affiliation":[{"name":"Department of Neurosurgery, Ehime University School of Medicine, Toon, Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Takuya","family":"Kondo","sequence":"additional","affiliation":[{"name":"Division of Diagnostic Pathology, Ehime University Hospital, Toon, Japan."}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Eiji","family":"Katayama","sequence":"additional","affiliation":[{"name":"Division of Diagnostic Pathology, Ehime University Hospital, Toon, Japan."}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Mashio","family":"Taniwaki","sequence":"additional","affiliation":[{"name":"Division of Diagnostic Pathology, Ehime University Hospital, Toon, Japan."}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Seiji","family":"Shigekawa","sequence":"additional","affiliation":[{"name":"Department of Neurosurgery, Ehime University School of Medicine, Toon, Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Hideaki","family":"Watanabe","sequence":"additional","affiliation":[{"name":"Department of Neurosurgery, Ehime University School of Medicine, Toon, Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Riko","family":"Kitazawa","sequence":"additional","affiliation":[{"name":"Division of Diagnostic Pathology, Ehime University Hospital, Toon, Japan."}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Takeharu","family":"Kunieda","sequence":"additional","affiliation":[{"name":"Department of Neurosurgery, Ehime University School of Medicine, Toon, Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"10894","published-online":{"date-parts":[[2023,3,17]]},"reference":[{"key":"10.25259\/SNI_1175_2022\/ref-1","doi-asserted-by":"crossref","first-page":"494","DOI":"10.1111\/j.1600-0404.1995.tb00452.x","article-title":"Neurologic manifestations of intravascular lymphomatosis","volume":"91","author":"Chapin","year":"1995","journal-title":"Acta Neurol Scand"},{"key":"10.25259\/SNI_1175_2022\/ref-2","doi-asserted-by":"crossref","first-page":"200","DOI":"10.1111\/bjd.17603","article-title":"Incisional random skin biopsy, not punch biopsy, is an appropriate method for diagnosis of intravascular large B-cell lymphoma: A clinicopathological study of 25 patients","volume":"181","author":"Enzan","year":"2019","journal-title":"Br J Dermatol"},{"key":"10.25259\/SNI_1175_2022\/ref-3","doi-asserted-by":"crossref","first-page":"3156","DOI":"10.1002\/1097-0142(19930515)71:10<3156::AID-CNCR2820711043>3.0.CO;2-O","article-title":"Intravascular lymphomatosis. 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