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一名表现不典型的具有挑战性的女性患者的早期胰腺鳞状细胞癌病例报告。

Case report of early pancreatic adenocarcinoma squamous type in a challenging female patient with vague presentation.

作者信息

Jaber Mohanad, Tahayneh Mohammed, Maraqa Mohammed, Ibrahim Mahmoud, Suboh Mahdi W, AbuAlrub Ibraheem

机构信息

Clinical Medicine Department, Faculty of Medicine, Palestine Polytechnic University, Hebron, Palestine.

Basic Medicine Department, Faculty of Medicine, Palestine Polytechnic University, Hebron, Palestine.

出版信息

Int J Surg Case Rep. 2025 Jul 7;134:111629. doi: 10.1016/j.ijscr.2025.111629.

Abstract

INTRODUCTION AND IMPORTANCE

Pancreatic tumors are aggressive malignancies. Pancreatic ductal adenocarcinoma (PDAC), rarely exhibits squamous differentiation, a variant associated with worse prognosis. PDAC in the body and tail of the pancreas often presents with vague symptoms, making early diagnosis difficult and requiring advanced imaging and a multidisciplinary approach for effective management.

CASE PRESENTATION

A 63-year-old woman presented with persistent epigastric pain radiating to the back. Initial tests and ultrasound were normal. After symptoms persisted, a CT scan and MRCP revealed a pancreatic mass. Biopsy confirmed PDAC with squamous differentiation. The patient underwent subtotal pancreatectomy with splenectomy. Post-surgery, she was scheduled for adjuvant chemotherapy.

CLINICAL DISCUSSION

This case highlights the challenges of diagnosing rare pancreatic cancer variants with nonspecific symptoms. Advanced imaging, biopsy, and immunohistochemistry are crucial for accurate diagnosis. While surgical resection with clear margins is key, adjuvant chemotherapy is essential due to high recurrence risks. A multidisciplinary approach can improve outcomes for these rare cancer subtypes.

CONCLUSION

Pancreatic cancer is a rare tumor that can't be excluded as a differential in any abdominal pain. Management of pancreatic cancer cases require multidisciplinary collaboration between surgery, radiology, pathology and oncology departments to achieve the best outcome for the patient.

摘要

引言与重要性

胰腺肿瘤是侵袭性恶性肿瘤。胰腺导管腺癌(PDAC)很少表现出鳞状分化,这种变体与较差的预后相关。胰腺体尾部的PDAC常表现为模糊症状,导致早期诊断困难,需要先进的影像学检查和多学科方法进行有效管理。

病例介绍

一名63岁女性出现持续的上腹部疼痛并放射至背部。初始检查和超声均正常。症状持续后,CT扫描和磁共振胰胆管造影(MRCP)显示胰腺有肿块。活检证实为伴有鳞状分化的PDAC。患者接受了胰腺次全切除术加脾切除术。术后,她被安排进行辅助化疗。

临床讨论

该病例突出了诊断具有非特异性症状的罕见胰腺癌变体的挑战。先进的影像学检查、活检和免疫组织化学对于准确诊断至关重要。虽然切缘清晰的手术切除是关键,但由于复发风险高,辅助化疗必不可少。多学科方法可以改善这些罕见癌症亚型的治疗结果。

结论

胰腺癌是一种罕见肿瘤,在任何腹痛的鉴别诊断中都不能排除。胰腺癌病例的管理需要外科、放射科(应为“放射科”,原文“radiology department”表述有误)、病理科和肿瘤科之间的多学科合作,以实现患者的最佳治疗效果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2fcd/12305306/df317bdeffed/gr1.jpg

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