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胰腺非霍奇金淋巴瘤,梗阻性黄疸的罕见病因。病例报告。

Pancreatic Non-Hodgkin Lymphoma, a rare cause for obstructive jaundice. A Case reports.

作者信息

B Pragalathan, K Indranath, A A Jenil, S Gobishangar

机构信息

Professorial Surgical Unit, University of Jaffna, Sri Lanka.

Teaching Hospital Jaffna, Sri Lanka.

出版信息

Int J Surg Case Rep. 2021 Jan;78:369-371. doi: 10.1016/j.ijscr.2020.12.071. Epub 2020 Dec 26.

Abstract

INTRODUCTION

Primary pancreatic lymphoma (PPL) is an uncommon condition. Clinical features of PPL are nonspecific & likely to be misrecognized as pancreatic malignancy.

CASE PRESENTATION

71 years old male patient presented with upper abdominal pain with obstructive jaundice.

CLINICAL FINDINGS AND INVESTIGATIONS

Examination reveals RHC tenderness and deep icteric. CT shows a large pancreatic head and uncinate process mass. Final diagnosis made with USS guided core biopsy which confirmed B cell, Non-Hodgkin Lymphoma (NHL).

INTERVENTION AND OUTCOME

Complete remission of PPL occurred following six cycles of chemotherapy with R-CHOP regimen.

RELEVANCE AND IMPACT

PPL is rare condition, accounts 1% of extra nodal lymphomas and 0.5% of malignant pancreatic neoplasm. Ultrasonography, Endoscopic ultrasonography, CT and MRI are the imaging modalities use to diagnose the pancreatic neoplasm. Biopsy of all pancreatic lesion is crucial which can diagnose curable condition such as PPL. Combined therapy with chemotherapy and radiotherapy without surgery is advisable for PPL.

摘要

引言

原发性胰腺淋巴瘤(PPL)是一种罕见疾病。PPL的临床特征不具特异性,很可能被误诊为胰腺恶性肿瘤。

病例介绍

一名71岁男性患者因上腹部疼痛伴梗阻性黄疸前来就诊。

临床检查与诊断

检查发现右季肋部压痛且黄疸较深。CT显示胰头和钩突有一个大肿块。最终通过超声引导下的核心活检确诊为B细胞非霍奇金淋巴瘤(NHL)。

干预措施与结果

采用R-CHOP方案进行六个周期的化疗后,PPL完全缓解。

相关性与影响

PPL较为罕见,占结外淋巴瘤的1%,胰腺恶性肿瘤的0.5%。超声、内镜超声、CT和MRI是用于诊断胰腺肿瘤的成像方式。对所有胰腺病变进行活检至关重要,因为这可以诊断出可治愈的疾病,如PPL。PPL建议采用化疗和放疗联合治疗,不进行手术。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96eb/7787919/cb412fe426a2/gr1.jpg

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