A case of primary pancreatic lymphoma followed in remision in the 9th year

Year 2018, Volume: 15 Issue: 2, 95 - 97, 14.08.2018

İdris Oruç , Zeynep Oruç Mehmet Küçüköner , Berat Evran Soylu Muhammet Ali Kaplan

Abstract

Primary pancreatic lymphoma (PPL) is a rare form of ekstranodal,
lymphomas, comprising 0.2-4.9% of pancreatic masses and <1% of all malignant
lymphomas. Due to the rarity of PPL and nonspecific clinical symptoms and
imaging, differentiation of PPL from adenocarcinoma is difficult without
histopathologic diagnosis. Many patients with primary pancreatic lymphoma are
diagnosed after radical surgery due to difficulties in diagnosis. Many patients
with primary pancreatic lymphoma can be diagnosed after radical surgical
treatments due to diagnostic difficulties. A 70-year-old patient presenting
with abdominal pain was detected to have pancreatic mass. The post-operative
pathologic outcome was reported as T-rich B-cell lymphoma. The patient was
followed with complete remission after receiving six cycles of chemotherapy.
This case report emphasizes the importance of distinguishing between pancreatic
lymphoma and adenocarcinoma because of the different treatment strategies and
prognoses.

Keywords

Lymphoma, Pancreas, Mass

Dokuzuncu yılında remisyonda izlenen primer pankreatik lenfoma tanılı bir olgu

Abstract

Primer pankreatik lenfoma ekstranodal lenfomaların nadir bir formudur. Tüm pankreatik neoplazmların %0.2-4.9’unu,tüm malign lenfomaların ise %1’den azını oluşturur. Pankreatik lenfomaların nadir olarak görülmesi, spesifik olmayan klinik semptomları ve görüntüleme bulgularının özgüllüğünün az olması nedeniyle histolojik tanı olmaksızın pankreatik adenokarsinomadan ayrımı zordur. Tanısal açıdan yaşanan zorluklar nedeniyle primer pankreatik lenfomalı bir çok hastanın tanıları radikal cerrahi tedaviler sonrasında yapılabilmektedir. Epigastrik ağrı şikayeti ile polikliniğimize başvuran 70 yaşında kadın bir hastada pankreas başında kitle tespit edildi. Opere edilen hastanın postoperatif patoloji sonucu diffüz büyük B hücreli lenfoma olarak raporlandı. Hastaya kemoterapi verildi ve tam remisyon elde edildi.Bu vaka sunumu, tedavi stratejileri ve prognozları farklı olduğu için pankreatik lenfoma ve adenokarsinomun ayrımının önemini vurgular.

Keywords

Lenfoma, Pankreas, Kitle

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