A Case Report on Duplex Appendix in a Patient with Ileocolocolic Intussusceptions

Yitagesu Aberra
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引用次数: 2

Abstract

Duplex cecal appendix is a rare anatomical variation. Approximately 100 cases of double cecal appendix have been described so far. Till now there is no report of duplex appendix serving as a lead point in a patient with intussusceptions. This case report presents the first case of such presentation for the first time. This 6 month old female child presented with vomiting and diarrhea of week duration. She was tachycaridic, tachypniec and febrile. On abdominal examination she had distended and tender abdomen with hyper tympanic sound on percussion. She was irritable and had a sunken eye ball. She had leaukocytosis (20.8 × 103), hypokalemia (3.3 mmol/l) and hyponatremia (125 mmol/l). Abdominal ultrasounds were suggestive of intussusception. After stabilizing the patient we operated her for possible pre-operative diagnosis of SBO secondary to Intussusception. Intra-operatively it was an Ileocolocolic intussusception with duplex appendix as a leading point. We did resection and anastomosis. Post operatively she was transfused with two units of blood (20 ml/kg), given IV antibiotics, analgesics and followed with vital sign sheet (Table 1). She started PO feeding after 36 hours post operation and discharged on the 7th day improved. The case is extremely important for the study of this possible anatomical variation and its association with intussusceptions. It also serves as an input for future studies in the area. Moreover, its association with the presence of other anatomical variations such as intestinal, genitourinary and bone is important. And reporting such a rare case is very essential in the development of surgical practice.
回肠-结肠-结肠肠套叠双阑尾1例报告
双盲肠阑尾是一种罕见的解剖变异。大约100例双盲肠阑尾已被描述到目前为止。到目前为止,还没有双阑尾作为肠套叠患者的先导点的报道。本病例报告首次提出这种表现的第一个病例。这个6个月大的女婴表现为呕吐和腹泻持续了一周。她心跳过速、心动过速、发热。腹部检查发现腹部肿胀、压痛,敲击时伴有高鼓室音。她脾气暴躁,眼球凹陷。患者有白细胞增多(20.8 × 103)、低钾血症(3.3 mmol/l)、低钠血症(125 mmol/l)。腹部超声提示肠套叠。稳定病情后,我们对她进行了手术,以便术前诊断继发于肠套叠的SBO。术中为以双阑尾为龙头的回肠-结肠-结肠肠套叠。我们做了切除和吻合。术后输注2单位血(20 ml/kg),静脉给予抗生素、镇痛药,随访生命体征单(表1)。术后36 h开始PO喂养,第7天病情好转出院。该病例对于研究这种可能的解剖变异及其与肠套叠的关系非常重要。它还可以作为该领域未来研究的输入。此外,它与肠道、泌尿生殖系统和骨骼等其他解剖变异的存在相关是重要的。报道这样一个罕见的病例对外科实践的发展是非常必要的。
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