Al Salkhadi Asham, Al Salkhadi Mohammad Ajwad, Hasan Ayham
Department of General Surgery, Mubarak Al Kabeer Hospital, Al-Jabriyah 32001, Kuwait.
Department of Radiology, Jordan University of Science and Technology, Irbid 22110, Jordan.
J Surg Case Rep. 2024 Nov 18;2024(11):rjae713. doi: 10.1093/jscr/rjae713. eCollection 2024 Nov.
Mucinous adenocarcinoma of the appendix (MAA) is a rare primary malignancy with an incidence of 0.01-0.2% and often presents as acute appendicitis. We present a case of a 61-year-old male who initially presented with right iliac fossa pain, worsening over 3 days, accompanied by appetite loss but no other symptoms. The patient's history included a splenectomy and epilepsy. Physical examination and computed tomography scan suggested a picture of acute appendicitis. He underwent an emergency laparoscopic appendectomy that was converted to open right hemicolectomy due to the mass's adherence to the cecum. The mass, at the cecum, originating from the appendix, measured 10 × 7 × 7 cm. Pathology confirmed a moderately differentiated MAA. Accurate diagnosis requires a combination of imaging and histopathology. The patient recovered well and was discharged on Day 6 postoperatively. We aim to highlight the importance of distinguishing MAA from acute appendicitis and the need for careful preoperative evaluation.
阑尾黏液腺癌(MAA)是一种罕见的原发性恶性肿瘤,发病率为0.01%-0.2%,常表现为急性阑尾炎。我们报告一例61岁男性患者,最初表现为右下腹疼痛,3天内加重,伴有食欲减退,但无其他症状。患者既往有脾切除术和癫痫病史。体格检查和计算机断层扫描显示为急性阑尾炎表现。他接受了急诊腹腔镜阑尾切除术,但由于肿块与盲肠粘连,手术转为开腹右半结肠切除术。位于盲肠、起源于阑尾的肿块大小为10×7×7厘米。病理证实为中度分化的MAA。准确诊断需要影像学和组织病理学相结合。患者恢复良好,术后第6天出院。我们旨在强调将MAA与急性阑尾炎相鉴别以及进行仔细术前评估的重要性。