Background/Introduction: Female genital tract lymphoma is an extremely rare diagnosis1 accounting for only 1.5% of extra nodal non-Hodgkin’s lymphoma and a meagre less than 0.5% of gynaecological cancer2. Primary lymphoma of cervix is considered less common compared to cervical involvement in a multi organ disease3. Majority of these rare cases are diagnosed during routine screening on Papanicolaou (Pap) cytology smear4.
Due to the limited number of primary lymphoma of the cervix, a standard regime has not been developed5.
This is a case report of a 73 year old non-English speaking background lady who presented to her obstetrician with one month history of post-menopausal bleeding per vaginum. Histology revealed a high grade large B cell non-Hodgkin’s lymphoma with a high proliferative index, expressing C-MYC protein in a high proportion of cells and CD10 and LCA positive on a cervical biopsy.
Objectives: This poster presents the rarity of cervical lymphoma; including its incidence, clinical presentation and diagnostic dilemma from benign conditions as well as treatment regime.
Methods (including type of data collected): Case report and literature search/review on Pubmed/MEDLINE. Comparing both in terms of presentation, diagnosis and treatment management.
Results: Patient has been diagnosed in a timely manner and appropriately managed as well as treated.
Conclusions: This presentation of cervical diffuse large B cell non-Hodgkin’s lymphoma highlights the importance of having an absolute open mind when working up patients presenting with common symptoms in gynaecology like bleeding per vaginum and understanding the different management approaches for these rare conditions.
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