Duodenal wall hematoma imitating a pancreatic tumor as a rare cause of obstructive jaundice - a case report.

Q4 Medicine
Michał Jan Nawracaj, Maria Miłkowska, Aleksandra Denkiewicz, Martyna Małek, Julia Maja Bartczak, Łukasz Pieczykolan, Wiktoria Suszek, Piotr Sosiński, Łukasz Hołubiuk, Weronika Walęcik-Kot
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引用次数: 0

Abstract

Obstructive jaundice is mostly caused by malignant lesions such as pancreatic head cancer and cholangiocarcinoma. Atypical benign conditions such as intramural duodenal hematoma (IDH), can imitate malignant processes in both clinical and radiological presentation. The diagnostic workup included computed tomography (CT), magnetic resonance cholangiopancreatography (MRCP), endoscopic retrograde cholangiopancreatography (ERCP), and endoscopic ultrasound (EUS) with biopsy. A 65-year-old patient was referred for assessment of obstructive jaundice and endoscopic retrograde cholangiopancreatography (ERCP). Initial presentation included hematemesis, anemia, cholestasis, and coagulopathy. Imaging (MRCP, CT) showed dilation of intra- and extrahepatic bile ducts and pancreatic duct, suggesting obstruction at the pancreatic head. CT also revealed a heterogeneous mass in the duodenum. ERCP demonstrated duodenal stenosis due to external compression and distal bile duct narrowing, and a self-expandable metal stent (SEMS) was inserted. Endoscopic ultrasound with biopsy revealed an intramural duodenal hematoma without malignant features. The patient's medical history was significant for multiple comorbidities and previous anticoagulation therapy. Follow-up imaging demonstrated complete regression of the hematoma, confirming its benign nature. The observed clinical course was consistent with spontaneous resolution; consequently, there was no need for surgical intervention. Intramural duodenal hematoma is a rare but important condition that may mimic pancreatic head tumors causing obstructive jaundice. Early detection using imaging techniques is critical to accurately establish the diagnosis. Early recognition facilitates conservative treatment and helps avoid unnecessary highly invasive surgical procedures.

类似胰腺肿瘤的十二指肠壁血肿是梗阻性黄疸的罕见病因- 1例报告。
梗阻性黄疸多由胰腺头癌、胆管癌等恶性病变引起。非典型良性疾病,如十二指肠壁内血肿(IDH),在临床和影像学表现上都可以模仿恶性过程。诊断检查包括计算机断层扫描(CT)、磁共振胰胆管造影(MRCP)、内镜逆行胰胆管造影(ERCP)和内镜超声活检(EUS)。一位65岁的患者被推荐评估梗阻性黄疸和内镜逆行胰胆管造影(ERCP)。最初的表现包括呕血、贫血、胆汁淤积和凝血功能障碍。MRCP、CT显示肝内、肝外胆管及胰管扩张,提示胰头梗阻。CT也显示十二指肠有不均匀肿块。ERCP显示十二指肠因外部压迫和远端胆管狭窄而狭窄,并插入自膨胀金属支架(SEMS)。内镜超声活检显示十二指肠壁内血肿,无恶性特征。患者的病史对多重合并症和既往抗凝治疗具有重要意义。随访影像显示血肿完全消退,证实其为良性。观察到的临床过程与自发消退一致;因此,不需要手术干预。十二指肠壁内血肿是一种罕见但重要的疾病,可能与胰头肿瘤相似,导致梗阻性黄疸。影像技术的早期检测对于准确诊断至关重要。早期识别有助于保守治疗,并有助于避免不必要的高侵入性手术。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Wiadomosci lekarskie
Wiadomosci lekarskie Medicine-Medicine (all)
CiteScore
0.80
自引率
0.00%
发文量
482
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