Case report: preoperatively diagnosed perforated Meckel’s diverticulum containing gastric and pancreatic-type mucosa
© The Author(s). 2017
Received: 17 February 2017
Accepted: 5 April 2017
Published: 11 April 2017
Meckel’s diverticulum is the most common congenital malformation of the gastrointestinal tract, and it represents a persistent remnant of the omphalomesenteric duct. Although it mostly remains silent, its infrequent occurrence is mirrored by the paucity of large series of data on it in the literature. Hemorrhage, obstruction and inflammation are most common complications of Meckel’s diverticulum. Perforation of Meckel’s diverticulum is considered very rare.
We present the case of a 17-year -old male, who presented to the emergency department with 1-day history of lower abdominal pain. CT of the abdomen suggested a perforated Meckel’s diverticulum, which was confirmed later at the exploratory laparotomy. Perforation was due to progressive inflammation and presence of gastric and pancreatic tissue found on histopathology.
Perforation of Meckel’s diverticulum is rarely suspected. Complications of Meckel’s diverticulum can be difficult to diagnose, and early recognition with timely operative intervention must occur in order to provide the best outcome for these patients. This is an interesting and unusual case of Meckel’s diverticulum perforation that highlights the importance of considering Meckel’s diverticulum as a differential diagnosis in every patient presenting with acute abdomen.
KeywordsMeckel’s diverticulum Perforated MD Complicated MD
Meckel’s diverticulum (MD) has long been discussed in medical literature. MD was first mentioned by Fadricius Hildamus in 1598 . It was named after the German anatomist Johann Friedrich Meckel, who described the embryological and pathological characteristics in an article published in 1809 . MD is the most common congenital abnormality of the gastrointestinal tract, occurring in about 2% of the general population [3–5]. MD is a remnant of the omphalomesenteric duct, which is normally obliterated by the 5th to 8th week of gestation. It is a true diverticulum, containing all three layers of the bowel wall, and it arises from the antimesenteric border of the bowel. Only 2% of cases show symptoms, and is found twice as common in males than in females . Most cases of MD are difficult to diagnose and are found incidentally during a surgical procedure for another reason. However, sometimes the presenting symptoms may guide the physician to suspect this pathology. The overall lifetime complication rate is approximately 4% . The most common presentation is bleeding, followed by intestinal obstruction, diverticulitis, intussusception, neoplasm and perforation . Perforation is very rarely seen, and it was reported in a review as being responsible for 0.5% of symptomatic MD . MD perforation was reported to be a consequence of acute inflammation of MD . Herein, we report a very rare case of perforated MD, which was identified prior to the operation. We provide an illustrative presentation, outlining one of the rare complications of MD in adults.
The patient was followed up in the outpatient settings for 6 months following his operation. He has recovered and has no active complaints.
Meckel’s diverticulum is the most common congenital anomaly of the gastrointestinal tract [3–5, 11]. The incidence ranges between 1 and 2%, with a lifetime complication risk of 4–6% . MD is a true diverticulum, usually found on the anti-mesenteric edge in the ileum [2, 12]. The majority of MD are asymptomatic and are incidentally discovered intraoperatively . Perforation is reported to be a consequence of acute inflammation of MD, but the exact percentage of this pathology has not been reported. Ferguson et al. published in a search of Medline and Embase around 40 case-reports of perforated MD over the past 30 years . Perforated MD may present as acute abdomen and resemble acute appendicitis . It is either caused by irritation of foreign body, like fish bone [16, 17], bay leaf, chicken bone, needles and button battery [18–20]. or following blunt abdominal trauma, which was first described by Park and Lucas in 1970 . Neoplastic causes, like GIST or leiomyoma, have been also reported [22, 23]. Perforation due to progressive inflammation of MD or ulcerating ectopic tissue was reported and was present in our case.
Diagnosis of MD is notably difficult, as the symptoms and imaging features are non-specific [9, 24]. CT scan and Ultrasound are not diagnostic because they can’t differentiate between a diverticulum and a loop of bowel . Meckel-scan with 99mTc-pertechnetate may diagnose MD. It can detect the presence ectopic gastric mucosa in cases of complicated MD and can also identify the site of gastrointestinal bleeding. Its accuracy was reported to be around 90% in pediatric series, and only 46% in the adult group . Less than 10% of symptomatic cases of MD are diagnosed preoperatively. In the reported case, perforated MD was diagnosed preoperatively on CT scan, which makes our case exceptional .
Surgical resection is considered the treatment of choice for the symptomatic MD. This can be achieved by diverticulectomy, segmental bowel resection and anastomosis and wedge resection. This is especially applicable when there is palpable ectopic tissue at the diverticular-intestinal junction, intestinal ischemia or perforation. In the reported case, the patient had perforation of a sessile MD. Resection of the involved bowel segment and anastomosis was indicated.
Meckel’s diverticulum perforation is very rare; however, it should be kept in mind as a differential diagnosis for every patient presenting with acute abdomen. In cases where the nature of the complication is likely to require surgical management, an early laparoscopic or open exploration should be performed in order to prevent the morbidity and mortality associated with late complications. The treatment should be based on the surgeon’s judgment and on the inherent characteristics of each patient.
Gastrointestinal stromal tumor
International medical center
Masood Iqbal, MD, Specialist, Emergency Department, IMC, Jeddah, KSA
Alsaid Amin, MD, Medical Imaging Department Chairman, Jeddah, KSA
Rafat Abu Shakra, MD, Pathology Consultant, Jeddah, KSA
Suhad Al Juhani, MD, General Surgery Resident, Jeddah, KSA
MI: Was the emergency physician who received the patient in ER and started initial management.
AA: The radiologist who suggested the diagnosis of perforated MD based on the CT imaging.
RA: The pathologist who examined the surgical specimen and provided the histological images provided in this report
Availability of data and materials
The datasets generated during and/or analysed during the current study are not publicly available because the Data were obtained from IMC Health Information System, which is a computer-based in-house system in our hospital. Data are available from the corresponding author on reasonable request.
GA: surgeon who performed the operation, reviewed the manuscript, wrote part of discussion and introduction. HA: literature review and case presentation, finalized the manuscript and submitted the paper for publication. All authors read and approved the final manuscript.
The authors declare that they have no competing interests.
Consent for publication
Written informed consent was obtained from the patient for publication of this Case report and any accompanying images. A copy of the written consent is available for review by the editor of this journal.
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