Autor: |
Taha A. Baiomy, Ola A. Harb, Ahmed A. Obaya, Loay M. Gertallah |
Jazyk: |
angličtina |
Rok vydání: |
2020 |
Předmět: |
|
Zdroj: |
Human Pathology: Case Reports, Vol 22, Iss , Pp 200459- (2020) |
Druh dokumentu: |
article |
ISSN: |
2214-3300 |
DOI: |
10.1016/j.ehpc.2020.200459 |
Popis: |
Background: Primary splenic lymphoma (PSL) is rare anatomical subtype of non-Hodgkin lymphoma which primarily originated from and limited to the spleen without other sites invasion, with a 6 months interval before lymphoma appearance in other locations. Case presentation: In the present report we described a case of a female patient aged 59 years old with pathologically confirmed PSL.The patient was with a left upper quadrant abdominal pain since 3 month. Radiological evaluation revealed diffuse splenomegaly. The patient underwent splenectomy and the histopathological examination of the spleen revealed high-grade non-Hodgkin B-cell lymphoma. Conclusions: It is important to put in consideration that PSL although a rare, but must be considered as a differential diagnosis, in a patient with splenomegaly and abdominal pain in absence of specific clinical findings. |
Databáze: |
Directory of Open Access Journals |
Externí odkaz: |
|