- Open Access
Intraoperative diagnosis of solitary cecal diverticulum not requiring surgery: is appendectomy indicated?
World Journal of Emergency Surgeryvolume 11, Article number: 1 (2016)
To compare experience with solitary cecal diverticulum (SCD) with literature on the indication for appendectomy in cases of solitary cecal diverticulitis.
We retrospectively reviewed all cases of SCD in our institution from September 2011 to March 2013. Data on sex, age, ethnic origin, presence of pain in the right iliac fossa, duration of symptoms, diagnosis, management, intraoperative findings, histologic examination, hospital stay, complications, and follow-up were reviewed and analyzed. We compared this to related literature reported between 2000 and 2015.
In the study period, 10 patients presented with an SCD. Male sex and Asian origin were predominant. All patients had pain in the right iliac fossa, with a duration of 2–5 days. In nine cases the diagnosis was made by clinical examination and laboratory testing. One patient who had undergone a previous appendectomy was diagnosed with SCD by computed tomography. This last patient was treated conservatively, four patients were treated with resection of the cecum “en bloc” with the last jejunal loop and appendix, and the other five patients were treated with appendectomies. Two patients had minor complications. All patients were followed up for a minimum of 12 to a maximum of 24 months. No recurrence was recorded in either the case treated conservatively or the cases treated by appendectomies.
In cases of operative but conservative treatment for SCD, appendectomy could be justified to avoid misdiagnosis in case of future episodes of solitary cecal diverticulitis.
The cecal diverticula described for the first time by Potier in 1912  remain a rare entity, especially if solitary, with an incidence between 1:50 and 1:300 of that of appendicitis . The incidence of solitary cecal diverticulum (SCD) in North America is low at about 1–2 %; in contrast, SCD is more common in the Orient, accounting for 43–50 % of all cases of colonic diverticulosis .
Pain in the right iliac fossa (RIF) is a common presentation to the emergency department of most hospitals. Preoperative diagnosis is invariably difficult. The most common clinical misdiagnosis of diverticular disease of the right colon is acute appendicitis , and it is then on the operating table that we are faced with the reality of the actual diagnosis. More than 70 % of patients with cecal diverticulitis underwent a surgical procedure with an erroneous indication . Other differential diagnoses to consider are urinary tract infection, ureteric colic, gastroenteritis, pelvic inflammatory disease, Crohn's disease , colonic malignancy, perforated foreign body reaction, and ileocecal tuberculosis . The correct diagnosis is very important because acute diverticulitis of the right colon without complications can be treated medically .
When patients are subjected to a surgical procedure in the presence of an SCD that affected the patient but did not require surgical treatment, the necessity of then performing an appendectomy (AP) is still debatable. The aim of the present study is to retrospectively report our personal experience with SCD, and to compare this with a review of the literature focusing on the indication of AP in the presence of cecal diverticulitis not requiring surgery.
Materials and methods
A retrospective analysis was performed on patients admitted to the Hamad General Hospital of Doha, Qatar from September 2011 to March 2013 with pain in the RIF. Sex, age, ethnic origin, duration of symptoms, diagnosis, management, intraoperative findings, histologic examination, length of hospital stay, complications, and follow-up of all patients affected by SCD were reviewed.
An extensive search for relevant literature between 2000 and May 07, 2015 was carried out using MEDLINE (PubMed) and Google Scholar with the language restricted to English, Italian, and French. The keywords used for the search were: ‘Right sided colon diverticulitis’, ‘caecum diverticulitis’, and ‘solitary cecum diverticula’. These keywords were used individually or with the Boolean operator ‘AND’.
We included articles that reported patient number, sex, age, duration of symptoms, diagnosis, type of surgical procedure, pathological report, compliance, recurrence, histopathologic examinations, length of hospital stay, and follow-up. Studies that did not clearly meet the inclusion criteria were excluded.
In the 18 months from September 2011 to March 2013, 2982 patients were evaluated and operated on for appendicitis at the Hamad General Hospital Department of Surgery. Ten of these patients were diagnosed with SCD with a ratio of 298.2:1, giving an incidence of SCD of 0.3 % or 1 in 300 APs. Nine of the 10 SCD patients were male, giving a 9:1 male to female ratio. All SCD patients were aged 19–40 years (mean age 30.4 years). Regarding nationality of the SCD patients, all patients were Oriental; there was one Indian, two Egyptians, one Sri Lankan, one Qatari, two Filipino, two Bangaladeshi, and one Syrian. The SCD patients presented for the first time to the Emergency Department with localized RIF pain of 2–5 days duration. All SCD patients except one were diagnosed with acute appendicitis on clinical examination. The diagnosis of appendicitis was based on the patients’ clinical presentation, and supported by a leukocytosis typical of acute appendicitis. However, one patient with pain for 5 days and a history of AP underwent a computed tomography (CT) scan and was managed conservatively; for this patient, a diagnosis of SCD was made preoperatively. Diagnosis of SCD for the remaining patients was made at the time of laparoscopy.
Of the 10 SCD patients, one had had a previous AP and was treated conservatively with antibiotic therapy, five patients were managed with AP alone, and four underwent an ileocecal resection. These last four patients were explored laparoscopically, and in all patients the surgery was converted to open surgery for the resection. The five patients managed with laparoscopic AP presented with an inflamed diverticulum that had not perforated; the appendix in these patients was removed to facilitate the diagnosis in case of secondary episode of RIF inflammation. All nine patients operated on (90 %) had a cecal mass; in four patients the flogosis did not permit us to distinguish the cecum from the appendix or the diverticulum, while in the other five patients it was still possible to identify the appendix and also the inflamed cecal diverticulum even in the presence of a cecal mass. In two of 10 cases (20 %) the cecal mass was located medially above the ileocecal junction, in four cases (40 %) the cecal mass was anterior, and in two cases (20 %) cases the cecal mass was located laterally. Two of 10 patients (20 %) had a perforation of their diverticulum; in one patient (10 %) this was treated with conservative antibiotic therapy, and in the other patient (10 %) this was treated with an ileocecectomy. All patients, including the nine that received surgery and the one that was treated conservatively, received intravenous antibiotics and gradually progressed on to a normal diet. The hospital stay varied from 4 to 10 days. Two patients had complications: one had urinary retention and another had a wound infection. All patients were given a follow-up examination, and all patients had no complaint after 1 month. All of these SCD patients have been followed up for a minimum of 12 to a maximum of 24 months, and no recurrence has been recorded in any case. However, the follow-up is limited as many of these patients are contractors who return to their native countries when they finish their period of work.
The histopathologic examinations of all four resected ileocecal specimens were reported as true solitary cecal diverticulitis. All nine appendices were reported as normal, including the four with the ileocecal specimen (Table 1).
A total of 19,794 published studies were screened from the sources listed. After examination of all titles, 19,689 papers were excluded as not relevant for reasons including being published before 2000, information repeated several times, containing data reported in other works, and the surgical procedure not being reported. Among the remaining 105 studies, the following were excluded: 14 articles were without data, 10 were case reports on children, 26 analyzed the diverticular disease without differentiating between the right and left sites, and 23 only partially met the inclusion criteria for our review (Fig. 1). A final total of 33 studies were included in the present study [2, 6, 7, 9–37].
In these 33 studies, a total of 1137 patients were analyzed. There were 643 males (56.5 %) and 477 females (41.9 %), excluding 18 patients (1.6 %) whose sex was not reported (, ). The mean patient age was 43.7 years. Only 22 studies reported the duration of symptoms, giving a mean of 2.9 days. The diagnosis was performed intraoperatively, or via CT scan or ultrasound (Table 2).
The treatment for SCD was antibiotic therapy in 523 patients (46.49 %), AP in 202 patients (17.95 %), diverticulectomy (DV) in 58 patients (5.15 %), AP + DV in 38 patients (3.38 %), AP + excision of diverticulum in one patient (0.09 %), suture of diverticulum in two patients (0.18 %), suture of cecum in one patient (0.09 %), cecum resection in two patients (0.18 %), AP + amputation of the cecal pole in one patient (0.09 %). Ascending (limited right) hemicolectomy was reported in one patient (0.09 %). Right hemicolectomy and ileo-transverse anastomosis was performed in 222 patients (19.73 %); ileocecal resection and anastomosis was performed in 55 patients (1.51 %). Yang et al. reported on 17 patients (1.51 %) who were not divided into right hemicolectomy and ileo-transverse anastomosis and ileocecal resection and anastomosis . Abscess drainage was performed in two patients (0.18 %). Kim et al. did not report the treatment in 13 patients (1.15 %) (Table 3) .
In 20 of the studies, the lesions were described intraoperatively. They were perforation of the diverticulum in 42 patients, inflamed cecal wall and perforation in two patients, diverticulum alone in eight patients, cecal mass in 18 patients, right colonic diverticulitis in one patient, and cecal diverticulitis in eight patients (Table 4).
Complications were reported for 73 patients (6.4 %), and 56 patients (4.9 %) were reported to have had recurrence of symptoms. In the group of patients with recurrence, 48 patients (85.8 %) were treated with conservative therapy, six patients (10.7 %) underwent AP, and two patients (3.6 %) underwent DV (Table 5).
Histopathologic examination was reported in only 13 studies. The mean length of hospital stay was 4.7 days, and only five studies reported follow-up (Table 6).
Diverticulosis is a predominantly Western disease, with a prevalence of 8.5 %. About 50 % of people older than 50 years are affected, and 85 % of these cases occur in the descending and sigmoid colon. Right sided diverticulosis is seen more commonly in the Oriental population, with an incidence as high as 71 %. Cecal diverticulae form 3.6 % of all colonic diverticulae, and 13 % of these develop inflammation at some time [6, 22, 23]. Males are more commonly affected (male:female ratio of 3:2) [6, 22, 23]. The median age at occurrence is 44 years [22, 23]. In our personal experience, the incidence of SCD in relation to appendicitis is as reported in the literature. However, the mean age and male:female ratio found in our study were different to the data reported in the literature. This is probably because Qatar has a high population of expatriate young males working on building the infrastructure.
Cecal diverticulae are classified as congenital or acquired. The congenital cecal diverticulae are true diverticulae; these include all the layers of the cecal wall and develop at 6 weeks gestation from a transient out-pouching of the cecum . The false or acquired diverticulae are similar to sigmoid diverticulae, and contain no muscular layer . Cecal diverticulae can also be classified as solitary or multiple, and can be found in the appendix, cecum, and ascending colon . The solitary cecal diverticulae are usually congenital and true as in our experience, while multiple cecal diverticulae are acquired and false .
In about 80 % of cases the cecal diverticulae are positioned 2.5 cm from the ileocecal junction, and about 50 % are on the anterior cecal wall and may cause peritonitis . When the cecal diverticulae are posterior, this may cause inflammatory masses that simulate carcinoma . In our study, none of the masses were due to posterior disease of the cecum wall. This is probably due to the fact that many of these patients arrive in the hospital only in the presence of severe pain that cannot regress with oral treatment, following repeated attacks that may also be due to microperforation causing localized peritonitis that regresses with oral treatment. So in this way repeated attacks can cause a cecal mass to form even if the diverticulum is positioned on the anterior wall of the cecum.
Acute appendicitis is the clinical diagnosis in 85 % of the cases of cecal diverticulitis . In the setting of inflammation, leukocytosis would be characteristic. Clinically, patients with SCD present with a long history of right lower quadrant abdominal pain, with the absence of systemic toxic signs and of nausea/vomiting . Unlike in appendicitis, the pain remains in the right lower quadrant instead of migrating from the epigastrium .
Only 10 of 5000 (0.2 %) radiological examinations would diagnose cecal diverticulitis in Oriental people ; this improves to 9 % if the patient has had a previous AP , and improves further to 65 % intraoperatively . The radiological diagnosis with an abdominal radiograph revealed a fecalith in 50 % of cases, and a barium enema may show the diverticulum as obliteration of its lumen because of surrounding inflammation and edema . Abdominal ultrasound demonstrated a hypoechoic area on a portion of a thickened cecal wall ; this radiological procedure has a sensitivity of 91.3 %, specificity of 99.8 %, and an accuracy of 99.5 % for the diagnosis of cecal diverticulitis . CT scans are being increasingly used; this radiological examination showed thickened cecal wall with an extraluminal mass associated with haziness and linear stranding of the pericecal fat . Magnetic resonance imaging can be used in case of equivocal ultrasound features or in case of young or pregnant patients who need to avoid ionizing radiation .
Despite advances in these radiological examinations, a correct preoperative clinical diagnosis occurs in only 4–16 % of cases . Between 65 and 85 % of macroscopic diagnosis of SCD is laparoscopic, especially in young females with atypical symptomology . In our case the majority of patients at our hospital are males, which can help with limiting the differential diagnoses. However, in our hospital we usually perform between 7 and 15 surgical procedures per night, and the majority of these are for acute appendicitis; in the absence of specific indications, the diagnosis is based on clinical examination and laboratory testing. In our study, the diagnosis of SCD was made via abdominal CT scan in one patient treated previously with AP, and in nine patients the diagnosis was intraoperative by laparoscopy. As the majority of cases of SCD are treated conservatively, we have chosen to perform the APs to avoid misdiagnosis in case of future inflammation of SCD. This can be useful especially in these patients coming from developing countries where frequently there are not sufficient tools to achieve diagnostic images; the anamnestic record of AP and the diagnosis of SCD can help in choosing the appropriate treatment and reserve surgical treatment for patients with complicated or evolving disease.
There are four grades of diverticulitis according to the management guidelines (ACS recommendations). Grade I: inflamed diverticulum; the treatment is conservative if the diagnosis is made preoperatively, the treatment is AP ± DV if the diagnosis is made intraoperatively. Grade II: inflamed mass. Grade III: localized abscess/fistula. For these two grades the treatment is conservative if the diagnosis is preoperative; if the diagnosis is intraoperative, the treatment is limited ileocecostomy or right hemicolectomy. Grade IV: perforation/ruptured abscess with generalized peritonitis; whether the diagnosis for this grade is pre- or intra-operative, the treatment is limited ileocecostomy or right hemicolectomy . Table 7 lists all treatment possibilities and associated advantages and disadvantages depending on the disease status.
The most commonly reported complications of SCD are inflammation (13 %), bleeding (15 %), hemorrhage, torsion and perforation (12 %) .
When diagnosed preoperatively, non-perforated cecal diverticulitis can be managed conservatively with intravenous antibiotics and supportive care with a caution that complicated recurrences are common (up to 20 %) . This therapy can also be used in cases of uncomplicated cecal diverticulitis diagnosed by laparoscopy . A skilled surgeon can conduct a simple DV or invagination of the diverticulum with AP by laparoscopy . In our case, the inflamed wall of the cecum was not treated because residents of fellows or specialists usually perform the procedures during the night and they do whatever is safest for the patients.
Ileocecal resection or right hemicolectomy should be considered in patients with marked inflammation, perforation, or torsion . In cases where the SCD is located on the posterior wall and tumor of the cecum is suspected, right hemicolectomy is mandatory . In a review of 49 patients, 40 % of patients treated with DV or antibiotics alone underwent subsequent hemicolectomy for persistence of the inflammatory process . In another review of 85 patients, less than 40 % were successfully treated with conservative therapy; in the group treated with AP, 29.2 % had a recurrence and 12.5 % were treated subsequently with right hemicolectomy . After surgical treatment for cecal diverticulitis, a mortality of 0 % was reported after ileocecal resection and of 1.8 % after right hemicolectomy .
In conclusion, antibiotic therapy remains the most commonly used treatment for SCD in the literature. In case of operative but conservative treatment, AP is justified to avoid misdiagnosis in case of future episodes of diverticular inflammation.
Stollman N, Raskin JB. Diverticular disease of the colon. Lancet. 2004;363:631–9.
Malek L, Sultan A, Abbas M, Al-Awadhi N. Perforated caecal diverticulitis mimicking an acute appendicitis: a case report. Cases J. 2009;2:7901.
Portier F. Diverticulite et appendicite. Bull Mem Soc Anat Paris. 1912;37:29–31.
Griffiths EA, Bergin FG, Henry JA, Mudawi AM. Acute inflammation of a congenital cecal diverticulum mimicking appendicitis. Med Sci Monit. 2003;9:CS107–9.
Lo CY, Chu KW. Acute diverticulitis of the right colon. Am J Surg. 1996;171:244–6.
Connolly D, McGookin RR, Gidwani A, Brown MG. Inflamed solitary caecal diverticulum - it is not appendicitis, what should I do? Ann R Coll Surg Engl. 2006;88:672–4.
Griffiths EA, Date RS. Acute presentation of a solitary caecal diverticulum: a case report. J Med Case Rep. 2007;1:129.
Wada M, Kikuchi Y, Doy M. Uncomplicated acute diverticulitis of the cecum and ascending colon: sonographic findings in 18 patients. AJR Am J Roentgenol. 1990;155:283–7.
Law WL, Lo CY, Chu KW. Emergency surgery for colonic diverticulitis: differences between right-sided and left-sided lesions. Int J Colorectal Dis. 2001;16:280–4.
Fang JF, Chen RJ, Lin BC, Hsu YB, Kao JL, Chen MF. Aggressive resection is indicated for cecal diverticulitis. Am J Surg. 2003;185:135–40.
Papaziogas B, Makris J, Koutelidakis I, Paraskevas G, Oikonomou B, Papadopoulos E, et al. Surgical management of cecal diverticulitis: is diverticulectomy enough? Int J Colorectal Dis. 2005;20:24–7.
Yang HR, Huang HH, Wang YC, Hsieh CH, Chung PK, Jeng LB, et al. Management of right colon diverticulitis: a 10-year experience. World J Surg. 2006;30:1929–34.
Basili G, Celona G, Lorenzetti L, Angrisano C, Biondi G, Preziuso E, et al. Laparoscopic treatment of caecal diverticulitis. Chir Ital. 2006;58:55–9.
Ruiz-Tovar J, Reguero-Callejas ME, Gonzalez PF. Inflammation and perforation of a solitary diverticulum of the cecum. A report of 5 cases and literature review. Rev Esp Enferm Dig. 2006;98:875–80.
Kurer MA. Solitary caecal diverticulitis as an unusual cause of a right iliac fossa mass: a case report. J Med Case Rep. 2007;1:132.
Hildebrand P, Kropp M, Stellmacher F, Roblick UJ, Bruch HP, Schwandner O. Surgery for right-sided colonic diverticulitis: results of a 10-years-observation period. Langenbecks Arch Surg. 2007;392:143–7.
Leung WW, Lee JF, Liu SY, Mou JW, Ng SS, Yiu RY, et al. Critical appraisal on the role and outcome of emergency colectomy for uncomplicated right-sided colonic diverticulitis. World J Surg. 2007;31:383–7.
Lee IK, Kim SH, Lee YS, Kim HJ, Lee SK, Kang WK, et al. Diverticuliyis of the right colon: tips for preoperative diagnosis and treatment strategy. J Korean Soc Coloproctol. 2007;23:223–31.
Karatepe O, Gulcicek OB, Adas G, Battal M, Ozdenkaya Y, Kurtulus I, et al. Cecal diverticulitis mimicking acute Appendicitis: a report of 4 cases. World J Emerg Surg. 2008;3:16.
Kachroo N, Sivakumar R, Hakim A, Semeraro D, Speake W. An unusual presentation of caecal diverticulitis. BMJ Case Rep. 2009;2009.
Telem DA, Buch KE, Nguyen SQ, Chin EH, Weber KJ, Divino CM. Current recommendations on diagnosis and management of right-sided diverticulitis. Gastroenterol Res Pract. 2009;2009:359485.
Cole M, Ayantunde AA, Payne J. Caecal diverticulitis presenting as acute appendicitis: a case report. World J Emerg Surg. 2009;4:29.
Kumar S, Fitzmaurice GJ, O'Donnell ME, Brown R. Acute right iliac fossa pain: not always appendicitis or a caecal tumour: two case reports. Cases J. 2009;2:88.
Butt WT. Caecal diverticulitis: a rare cause of right iliac fossa pain. Ir Med J. 2009.
Matsushima K. Management of right-sided diverticulitis: A retrospective review from a hospital in Japan. Surg Today. 2010;40:321–5.
Kim MR, Kye BH, Kim HJ, Cho HM, Oh ST, Kim JG. Treatment of right colonic diverticulitis: the role of nonoperative treatment. J Korean Soc Coloproctol. 2010;26:402–6.
Paramythiotis D, Papadopoulos VN, Michalopoulos A, Panagiotou D, Panidis S, Digkas E, et al. Inflammation of solitary caecal diverticula: a rare aetiology of acute abdominal pain: an experimental study. Tech Coloproctol. 2011;15:S43–5.
Radhi J, Ramsay JA, Boutross-Tadross O. Diverticular disease of the right colon. BMC Res Notes. 2011;4:383–7.
Uwecheue RU, Richards ER, Kurer M. Stapled diverticulectomy for solitary caecal diverticulitis. Ann R Coll Surg Engl. 2012;94:e235–6.
Kwon JW, Kim BS, Park HC, Oh HK, Shin R, Ryoo SB, et al. Surgical treatment of complicated right colonic diverticulitis: laparoscopic versus open surgery. Surg Endosc. 2012;26:2926–30.
Issa N, Paran H, Yasin M, Neufeld D. Conservative treatment of right-sided colonic diverticulitis. Eur J Gastroenter Hepatol. 2012;24:o1254–8.
Tan KK, Liu JZ, Shen SF, Sim R. Emergency surgery in colonic diverticulitis in an Asian population. Int J Colorectal Dis. 2011;26:1045–50.
Tan KK, Wong J, Sim R. Non operative treatment of right-sided colonic diverticulitis has good long-term outcome: a review of 226 patients. Int J Colorectal Dis. 2013;28:849–54.
Kroening HL, Rai S. Caecal diverticulitis, an uncommom mimic of appendicitis. BMJ Cas Rep. 2013.
Gilmore T, Jordan C, Edelstein E. Right-sided diverticulitis mimics appendicitis. J Emerg Med. 2013;44:e29–32.
Kahveci S, Tokmak TT, Yıldırım A, Mavili E. Acute right-sided colonic diverticulitis mimicking appendicitis: a report of two cases. J Clin Ultrasound. 2013;41:238–41.
Cristaudo A, Pillay P, Naidu S. Caecal diverticulitis: presentation and management. Ann Med Surg. 2015;4:72–5.
Abogunrin FA, Arya N, Somerville JE, Refsum S. Solitary caecal diverticulitis – a rara cause of right iliac fossa pain. Ulster Med J. 2005;74:132–3.
Chiu JH, Lin JT, Lin JK, Leu SY, Liang CL, Wang FM. Diverticular disease of the colon. J Surg Asso. 1987;20:102–8.
Birnbaum BA, Wilson SR. Appendicitis at the millennium. Radiology. 2000;215:337–48.
Williams KL. Acute solitary ulcers and acute diverticulitis of the ceacum and ascending colon. Br J Surg. 1960;47:351–8.
Chou YH, Chiou HJ, Tiu CM, Chen JD, Hsu CC, Lee CH, et al. Sonography of acute right side colonic diverticulitis. Am J Surg. 2001;181:122–7.
Cobben LP, Groot I, Blickman JG, Puylaert JB. Right colonic diverticulitis: MR appearance. Abdom Imaging. 2003;28:794–8.
Hall J, Hammerich K, Roberts P. New paradigms in the management of diverticular disease. Curr Probl Surg. 2010;47:680–735.
Peltokallio P, Tykkä H, Myllärniemi H. Solitary diverticulum of the caecum and its complications. Ann Chir Gynaecol Suppl. 1977;66:230–3.
Lane JS, Sarkar R, Schmit PJ, Chandler CF, Thompson Jr JE. Surgical approach to caecal diverticulitis. J Am Coll Surg. 1999;188:629–34.
The authors declare that they have no competing interests.
KRM and AA made substantial contributions to the study conception and design, and were responsible for acquisition of data, analysis and interpretation of data. KRM, AA, KM, and TA were involved in drafting the manuscript. Di CI critically revised the manuscript for important intellectual content. KM and Di C I gave final approval of the version to be published. KRM, AA, KM, TA, and Di C. I agree to be accountable for all aspects of the work in ensuring that questions related to the accuracy or integrity of any part of the work are appropriately investigated and resolved. All authors read and approved the final manuscript.