Bains Lovenish, Bahadur Akshay, Lal Pawan, Bhatia Rahul, Singh Nirmala, Kaur Daljit
Department of Surgery, Maulana Azad Medical College, New Delhi, India.
Department of Surgery, Dr. Hedgewar Arogya Sansthan, Delhi, India.
Case Rep Gastroenterol. 2021 Jun 17;15(2):525-532. doi: 10.1159/000514775. eCollection 2021 May-Aug.
Epiploic appendagitis (EA) is inflammation of epiploic appendages, which are pedunculated fatty structures, extend from the cecum to the rectosigmoid junction, and are covered by the peritoneum. Torsion, infarction, and inflammation of it present with acute lower abdominal pain and localized tenderness in a well-looking patient. It poses as diagnostic conundrum due to its rarity and not picked by conventional radiography. A 50-year-old male presented with pain in RLQ for past 1 day, which kept on increasing without any other symptoms. His abdomen was soft with tenderness localized to the right lower quadrant (RLQ), classically at McBurney's point along with mild peritonism. Rest laboratory test, chest, and abdominal X-ray were normal except slight leukocytosis. Ultrasound was inconclusive. A working clinical diagnosis of appendicitis was made. Patient did not consent for surgery and was started on antibiotics with pain killers. With no significant improvement, he underwent CT scan which revealed focal area of soft-tissue attenuation along the lateral wall of ascending colon with fat stranding. He was diagnosed as EA and improved on conservative treatment. EA of RLQ of abdomen mimics acute appendicitis and can be considered as an uncommon differential diagnosis in presence of radiological findings of normal-appearing appendix. CT is the investigation of choice, and treatment is essentially conservative. Further, if appendix is found normal at exploration, surrounding epiploic appendages of the cecum and ascending colon should also be evaluated carefully for inflammation/hematoma/gangrene, besides looking for Meckel's diverticulum.
网膜附件炎(EA)是网膜附件的炎症,网膜附件是有蒂的脂肪结构,从盲肠延伸至直肠乙状结肠交界处,并被腹膜覆盖。其扭转、梗死和炎症表现为外观良好的患者出现急性下腹痛和局部压痛。由于其罕见且常规放射检查无法发现,它构成了诊断难题。一名50岁男性在过去1天出现右下腹疼痛,疼痛持续加剧且无其他症状。他的腹部柔软,压痛局限于右下腹(RLQ),典型部位在麦氏点,伴有轻度腹膜炎。其余实验室检查、胸部和腹部X线检查均正常,仅白细胞轻度增多。超声检查结果不明确。初步临床诊断为阑尾炎。患者不同意手术,开始使用抗生素和止痛药治疗。由于病情无明显改善,他接受了CT扫描,结果显示升结肠侧壁有软组织密度减低的局灶性区域,伴有脂肪条索影。他被诊断为网膜附件炎,经保守治疗后病情好转。腹部右下腹的网膜附件炎酷似急性阑尾炎,在阑尾影像学表现正常的情况下可被视为一种罕见的鉴别诊断。CT是首选的检查方法,治疗基本上是保守的。此外,如果在探查时发现阑尾正常,除了寻找梅克尔憩室之外,还应仔细评估盲肠和升结肠周围的网膜附件是否有炎症/血肿/坏疽。