Sellar B lymphoblastic lymphoma mimics pituitary apoplexy with newly discovered gene mutations in TP53 and PAX5: A case report

Sellar B lymphoblastic lymphoma mimics pituitary apoplexy with newly discovered gene mutations in TP53 and PAX5: A case report

Lymphoblastic lymphoma (LBL) is a rare tumor that accounts for approximately 2-4% of all non-Hodgkin lymphomas, and less than 20% of LBLs are derived from B cells. B- Lymphoblastic lymphoma (B-LBL) often presents as bone marrow and peripheral blood lesions, and is very rare to present as a seller ma...

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Veröffentlicht in:Frontiers in oncology 2023-02, Vol.13, p.1087232
Hauptverfasser: Wang, Yi, Yang, Yajun, Wang, Qiuxia, Wang, Ce, Xu, Xinjuan, Wang, Dongao, Bai, Feirong, Li, Panpan, Huang, Xintao
Format: Artikel
Sprache:eng
Schlagworte:
B-LBL
gene mutation
Oncology
Pax5
rare
sellar tumor
TP53
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Zusammenfassung:Lymphoblastic lymphoma (LBL) is a rare tumor that accounts for approximately 2-4% of all non-Hodgkin lymphomas, and less than 20% of LBLs are derived from B cells. B- Lymphoblastic lymphoma (B-LBL) often presents as bone marrow and peripheral blood lesions, and is very rare to present as a seller mass. We report a case of sellar B lymphoblastic lymphoma mimicking pituitary apoplexy, and review its diagnosis and treatment process, combined with the literature to deepen the understanding of sellar tumors.
ISSN:2234-943X
2234-943X
DOI:10.3389/fonc.2023.1087232