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Case report and review of the literature of primary central nervous system lymphoma of the fourth ventricle.
Kojima, Yuichiro; Nakajo, Kosuke; Ichinose, Tsutomu; Morikawa, Yoichiro; Osawa, Masahiko; Goto, Takeo.
Afiliação
  • Kojima Y; Department of Neurosurgery, Osaka Metropolitan University, Osaka, Japan.
  • Nakajo K; Department of Neurosurgery, Osaka Metropolitan University, Osaka, Japan.
  • Ichinose T; Department of Neurosurgery, Osaka Metropolitan University, Osaka, Japan.
  • Morikawa Y; Department of Hematology, Sumitomo Hospital, Osaka, Japan.
  • Osawa M; Department of Pathology, Osaka Metropolitan University, Osaka, Japan.
  • Goto T; Department of Neurosurgery, Osaka Metropolitan University, Osaka, Japan.
Surg Neurol Int ; 13: 529, 2022.
Article em En | MEDLINE | ID: mdl-36447844
ABSTRACT

Background:

Primary central nervous system lymphoma of the fourth ventricle is very rare. We present a case of primary central nervous system lymphoma originating from the fourth ventricle and review cases reported in the literature. Case Description A 54-year-old man with no previous medical history presented with headache and nausea. Magnetic resonance imaging showed a homogeneously enhancing tumor in the fourth ventricle and obstructive hydrocephalus. We performed biopsy of the tumor, which was diagnosed pathologically as diffuse large B-cell lymphoma. Although the tumor disappeared after 5 cycles of R-MPV regimen, the patient required repeated ventricular drainage and finally received a ventriculoperitoneal shunt. Complete response was achieved after 2 cycles of high-dose cytarabine chemotherapy with an autologous peripheral blood stem cell transplant. There was no sign of recurrence at 20 months after biopsy.

Conclusion:

Morbidity arising due to radical resection/radiotherapy of resistant primary central nervous system lymphoma originating from the fourth ventricle could be prevented by ventriculoperitoneal shunting with chemotherapy and autologous blood stem cell transplantation.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article