Qureshi Aneeqa, Ali Huzafa, Gyawali Jeevan, Tariq Aisha, Kamran Maheen
Radiology, Aga Khan University Hospital, Karachi, PAK.
Internal Medicine, Combined Military Hospital (CMH) Multan Institute of Medical Sciences, Multan, PAK.
Cureus. 2024 Sep 3;16(9):e68512. doi: 10.7759/cureus.68512. eCollection 2024 Sep.
Duodenum inversum is a rare congenital anomaly in which the proximal duodenum travels posteriorly and superiorly before crossing the midline, often presenting asymptomatically. Clinical features can include epigastric pain, nausea, and abdominal distension. This case report describes a 35-year-old female who presented with right hypochondrial pain. A CT scan revealed that the third part of the duodenum followed an upward and vertical course, crossing the midline at a higher level than usual, thus confirming the diagnosis of duodenum inversum. Despite the absence of obstruction, conservative medical management was employed to address the symptoms. This case highlights the importance of considering duodenum inversum in the differential diagnosis of right hypochondrial pain and underscores the value of modern imaging techniques in accurate diagnosis. Awareness of this rare condition can facilitate timely and effective management.
十二指肠反位是一种罕见的先天性异常,其中十二指肠近端在越过中线之前向后上方走行,通常无明显症状。临床特征可包括上腹部疼痛、恶心和腹胀。本病例报告描述了一名35岁女性,她表现为右季肋部疼痛。CT扫描显示十二指肠第三部呈向上垂直走行,在比正常更高的水平越过中线,从而确诊为十二指肠反位。尽管没有梗阻,但采用了保守药物治疗来缓解症状。本病例强调了在右季肋部疼痛的鉴别诊断中考虑十二指肠反位的重要性,并强调了现代成像技术在准确诊断中的价值。认识到这种罕见疾病有助于及时有效的治疗。