%0 Case Reports
%T [A case of primary central nervous system lymphoma of the sellar region presented with panhypopituitarism].
%A Seki A
%A Henmi F
%A Ito S
%A Uruga H
%A Arisawa K
%A Uesaka Y
%J Rinsho Shinkeigaku
%V 64
%N 5
%D 2024 May 24
%M 38658327
暂无%R 10.5692/clinicalneurol.cn-001941
%X The patient is a 41-year-old woman. She presented with vomiting and lightheadedness, and blood tests showed a generalized decrease in pituitary hormones and hyperprolactinemia. A head MRI showed increased signal intensity lesions on FLAIR image in the pituitary stalk, corpus callosum, periventricular area of the fourth ventricle, and superior cerebellar peduncle. The lesions were homogeneously enhanced, and a brain biopsy confirmed the diagnosis of primary diffuse large B-cell lymphoma of the central nervous system, and chemotherapy was started. Although the suprasellar region is a rare site for primary central nervous system lymphoma (PCNSL), it should be diagnosed early by biopsy.