A Rare Case of Spontaneous Remission and Relapse of a Primary Central Nervous System Lymphoma
Texto
Documentos relacionados
Furthermore, when a patient presents a suspected bone lesion and this is biopsied, it should be noted that for a correct diagnosis, a correlation should be made between the
Incidence and risk factors of central nervous system relapse in histologically aggressive non-Hodgkin’s lymphoma uniformly treated and receiving intrathecal central nervous
This report is a review of the most relevant contributions of nonconventional magnetic res- onance techniques to the imaging diagnosis of primary central nervous system lymphoma,
This tubulointerstitial nephritis and uveitis case makes us suggest that this rare syndrome should be considered in the differential diagnosis of unex- plained
The differential diagnosis should be made with other situations where the patient presents primary amenorrhea and normal secondary sexual characteristics, such as congenital absence
Primary central nervous sys - tem (CNS) lymphomas account for up to 6% of brain neoplasms and 1–6% of extranodal lymphomas; approximately 90% of pri - mary CNS lymphomas
The purpose of this study is to re p o rt and discuss a rare case of primary meningeal high grade Burkitt- type lymphoma, presenting as the first clinical man- ifestation of
In a case of pineal gland lymphoma reported in the literature, the lesion appeared to be similar to primary tumors of pineal origin (pineocytoma and pineoblas- toma), or even