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17 Prophylactic Appendectomy
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Fig. 17.2 Amyand hernia (arrow) is seen in the CT coro­nal section
to intestinal malrotation, IA is added to the procedure.
Some authors suggest appendectomy in cases with appendix (De Garengeot hernia) in the ingui­nal hernia sac (Amyand hernia, Fig.
17.2) or the
femoral hernia sac during inguinal hernia surgery [24]. IA is also performed during hernia surgeries. Dens adhesions occur after the wide abdominal defects are covered with mesh, and it may makes difcult for subsequent surgical entries. Dilek et al. considering that the intense brosis that will occur after mesh applications for the repair of giant inci­sional hernia would make subsequent operations difcult, they performed IA in 23 incisional hernia cases in their series of 64 IA (2001) cases [25]. However, some authors do not recommend appen­dectomy especially in cases with mesh application and in cases with normal appendix [26].
There are some studies that incidental appen-
dectomies are performed in addition to laparo-
185
scopic cholecystectomy, bariatric surgery, cardiac surgery, urological procedures, trauma surgery, and transplantation [
14, 27, 28]. While there are
authors that encourage appendectomy during bariatric procedures for obesity, there are also those who do not recommend it in cases where it is difcult to dissect the appendix in super obese [29]. Akbulut etal. (2020) reported that they did 170 incidental appendectomies in 1910 cases performing living donor hepatectomy, as a result of histopathological examination, they found normal appendix in 137 cases, brotic changes in 13 cases, acute appendicitis in 6 cases, Enterobius vermicularis in 5 cases, lymphoid hyperplasia in 4 cases, and various types of neoplasia in 7 cases. They also concluded that inspecting the appendix and seeking morphological changes could con­tribute to making an appendectomy [30].
The appendix is often removed during onco­logical surgery. In patients with Wilms tumor, appendectomy is performed together with nephrectomy. Especially in pediatric oncology cases, it is recommended to remove the appendix during surgery due to the risk of developing an acute abdomen due to chemotherapy and neutro­penic enterocolitis [12]. However, IA is not rec­ommended for patients with severe comorbidity, using immunosuppressants, vascular grafts and over 60years of age [3, 25].
It has been reported in many studies that inci­dental appendectomies have no negative effects on perioperative morbidity and mortality. It was reported that there was no signicant difference in morbidity after inguinal hernia surgery, inci­sional hernia, and hysterectomy operations [
13, 19, 31, 32]. While there was no signicant differ-
ence between Pollock and Evans’s series that underwent laparotomy, cholecystectomy, and IA, and antibiotics were used, the risk of infection was found to be higher in the series that did not use antibiotics [33]. However, there are also series that undergo laparoscopic cholecystec­tomy and IA and report that there is no signicant difference [34]. Strom et al. (1983) found that incidental appendectomies in patients undergo­ing laparotomy due to trauma and without surgi­cal pathology signicantly increased morbidity. In another prospective study of the same author
186
and colleagues, they reported that there was no signicant difference in morbidity between the appendectomy group and the non-appendectomy group during the laparotomy [28]. Morris etal. (1987) reported that 210 patients who underwent laparotomy due to Hodgkin’s disease, IA were added to procedure in 130 patients and there was no signicant difference in terms of morbidity. On the other hand, there are also publications reporting that the addition of IA prolongs wound infection and hospital stay while performing lap­aroscopic cholecystectomy [35].
There is a general opinion that IA prevents future appendicitis and complications. In many epidemiological studies in the literature, it has been reported that 20–25 IA prevents one future appendicitis and its possible complications [1, 3]. In the literature, abnormal pathological ndings were found in 16–73% of the cases in histopatho­logical examination of the patients who were considered to have normal appendix during lapa­rotomy [3, 13, 36]. With the IA, as expressed in the Turkish statement of “shooting two birds with one stone” the patient will be free from two prob­lems: single anesthesia, single hospitalization, one laparotomy, and the risk of appendicitis in the future and associated complications.
17.3.2 Prophylactic Appendectomy
Prophylactic appendectomy (PA) can be dened as the removal of the appendix without any fur­ther action. Indications and risks should be deter­mined in patients for PA. Decisions should be made by talking to the patient or relatives for diagnosis and surgery. Morbidity and mortality are undesirable. PA is performed for many rea­sons (Table17.1).
Fecalith or appendicolith formed within the appendix are among the most common causes of appendicitis (Fig. 17.3). In clinical studies, the risk of recurrence of appendicitis has been reported to be 72% in patients with appendico­lith. Interval appendectomy is recommended for patients who previously had attacks due to feca­lith or appendicolith [37]. In the retrospective computed tomography scan of 2913 patients of
O. N. Dilek et al.
Fig. 17.3 Fecalitis is seen (Arrow) in the appendix
18years or younger of age, Rollins etal. (2010) revealed appendicoliths in 75 cases (2.6%) [38].
Appendix foreign bodies are very rare enti­ties. Peristaltic strength of the appendix may not be enough to push foreign bodies into the cecum. Metal and similar objects more massive than the gravity of the appendix content settle in the chan­nel. However, foreign bodies rarely (0.0005%) can cause appendicitis [39]. Foreign bodies rarely show symptoms, and most are detected by chance during examinations. There is no need to remove foreign bodies in the appendix routinely. However, long, thin, and sharp-edged foreign bodies should be initially removed endoscopi­cally. In cases that cannot be removed, PA should be recommended [40]. There are also authors suggesting routine appendectomy on foreign bodies detected in young children [41]. In cases where mercury taken with mercury poisoning accumulates in the appendix, symptoms of chronic poisoning may be encountered. In the case of mercury poisoning, a medical and endo­scopic approach can be treated as well as authors are recommending PA [42]. It has been reported that the barium meal used during radiological examinations may accumulate in the appendix and cause appendicitis. Patients undergoing such radiological procedures should be informed that appendicitis and PA are recommended in symp­tomatic patients [43].
17 Prophylactic Appendectomy
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187
a
Fig. 17.4 Normal (a) and complicated (b) cecum diverticulum (arrow) and normal appendix (arrowhead) are seen in two different patients’ abdominal CT images
b
Although appendix diverticulum is very rare, PA is recommended in clinical series due to the risk of malignancy ranging from 7.1 to 47.8% and high risk of confusion with mucocele (9.8%– 33%) [4446]. Right colon diverticula often con­fuse clinically with appendicitis (Fig. 17.4). Abdominal tomography is useful in the differen­tial diagnosis. In the right colon diverticulitis series of 113 cases of Yang et al. (2008), 56 patients were diagnosed correctly, and medical treatment was performed, while 51 patients were operated with the diagnosis of acute appendicitis. There are also studies suggesting PA after medi­cal treatment in patients diagnosed with right colon diverticulitis [
47].
In recent years, the removal of luminal pathologies endoscopically and by the mucosal
Fig. 17.5 The abdominal CT axial section shows the clips in the radix and congested appendix (arrow) of our patient who underwent endoscopic resection for the lesion in the cecum
resection has started to be made increasingly. In such a case, we performed PA in a patient with edema and inammation in the appendix due to the clips placed on the control computed tomog­raphies taken after the EMR performed close to the appendix radix (Fig.17.5).
There are many studies on whether the para- sites cause appendicitis in the appendix. The most common parasites found in the appendix are helminths (Enterobius vermicularis, Schistosoma spp, Taenia spp, Trichuris trichiura,
and Ascaris lumbricoides) and protozoa (Entamoeba histolytica, Balantidium coli, and Cryptosporidium parvum). The parasites are thought to cause appendicitis by blocking the lumen, leading to lymphoid hyperplasia or inammation. The frequency of parasites in the appendix varies depending on the countries’ socioeconomic levels and eating habits. Parasites were detected in 0.5% of cases in a study from Hong Kong, 5.5% of cases in Oman, and 16% of
188
O. N. Dilek et al.
cases in Malaysia [48, 49]. The most common parasite in the appendix is Enterobius vermicu- laris, and its incidence has been reported between
0.2% and 41.8% (average 4.5%) [50, 51]. The incidence of appendicitis in appendixes with par­asites is very different in clinical series. In the literature, Zakaria et al. (2013) reported the appendicitis rate as 5.5% of their 1600 cases series. It was reported as 14.6% in Hong Kong series, 42.5% in Malaysia, and 81.3% in Pasupati series [4850]. It has been reported in many series that the incidence of parasites in the lumen of the appendix and the risk of appendicitis is very low, and the main cause of appendicitis is not. There is no consensus on performing PA due to the presence of parasites in the appendix. Anti- parasitic therapy should be initiated in those with or without appendectomy.
17.4 Miscellaneous Conditions
Chronic appendicitis is an entity characterized by chronic inammation in the appendix wall, which is shown as the cause of chronic abdomi­nal pain in the clinic. Occasionally, an acute
abdomen was held responsible for intestinal obstruction and perforations [52]. However, due to the difculties in its diagnosis, it can be accepted as an entity that has not been consensus. It is frequently encountered as a histopathologi­cal diagnosis in prophylactic appendectomy series in the clinic. In their series of 748 cases by Schumacher and Schwartz (1986), they reported chronic appendicitis in 27% of cases and normal appendix in 73% [36]. In another PA series, appendectomy was performed due to chronic pel­vic pain in 15 cases, and their histopathological analysis demonstrated that chronic appendicitis in 4 cases, malignancy in one case, acute appen­dicitis in one case, and normal appendix in 9 cases [13]. In 269 cases of appendectomy series of Leardi et al., chronic appendicitis was diag­nosed in 38 cases (14.2%). In their postoperative follow-up, they observed that 33 of the patients’ abdominal pain disappeared. They concluded that chronic appendicitis might have a role in
recurrent abdominal pain, and PA may be effective [53].
Plastron appendicitis may occur when the omentum surrounds the appendix in cases of appendicitis that progresses towards the perfora­tion and abscess formation. As a complication of appendicitis, more than 90% of cases improve with medical treatment and drainage performed in plastron appendicitis cases. Acute appendicitis recurs again in 5–26% of the recovered cases. While the risk of recurrence of appendicitis increases in the rst 6months, it decreases after the rst year. In such cases, two approaches are recommended. Mentula etal. (2015) recommend surgery in the early period (acute phase) as a fewer follow-up, fewer hospital admissions, fewer patients are admitted, and fewer interven­tional procedures will be performed [54]. There is also more risk of malignant neoplasia in 0.7% to 3% of patients with plastron appendicitis, and the risk of malignancy is higher than 40years of age. In the early stages, this risk can be elimi­nated with therapeutic appendectomy [5558]. A group of authors suggests that the medical approach should be preferred in the early period, and the interval appendectomy should be per­formed after 3months because it contains fewer complications. It is also recommended to per­form MRI before surgery [55, 57]. Besides, some authors stated that follow-up with MRI would be sufcient.
There are some speculations and many research about the increased risk of cancer in patients who have undergone appendectomy in the past, and their relationship with cancer has not been found [3]. However, in a retrospective cohort study with broad participation from Taiwan in recent years, it has been reported that developing colon cancer is 1.14 times higher in people who underwent an appendectomy and followed for 14 years (12.8 times). In the same study, they reported that the risk of developing colorectal cancer is much higher in the follow-up of patients undergoing an IA.Interestingly, it is known that a colon carcinoma should take about 10 years to develop from a polypoid lesion; this period was found between 1.5 and 3.5years postoperatively
17 Prophylactic Appendectomy
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189
after appendectomy [59]. Age-related changes in the intestinal ora and the immune system are known to be weakened due to age, and there is insufcient clinical data on the relationship of the event to appendectomy. It is known that genetic, nutritional, and environmental factors play an important role in the development of colon can­cer. Prospective clinical studies with broad par­ticipation are needed to reveal the relationship between appendectomy and colorectal cancer.
Although the appendix is thought to play a role in the immune system due to its lymphoid tissue content, there is insufcient data on the negative effect of appendectomy on the immune system and homeostasis [60]. There are also studies on the natural and dense microbiota in the appendix, which is a “safe house,” that it plays an important role in the regulation of the ora (microbiota and biolm) in the colon, and changes occur in the colon ora after appendec­tomy [61]. In the literature, there are studies reported that the risk of developing Crohn’s dis­ease increases 1.6–2.1 times in individuals who underwent appendectomy, or a decrease in the incidence of inammatory bowel diseases, espe­cially ulcerative colitis [2, 62]. There are even studies reporting that patients with ulcerative colitis have decreased immunosuppressive medi­cation needs, and relapses and symptoms decrease after appendectomy. However, all these data need to be investigated with large prospec­tive series [63]. While there are more than 500 types of bacteria in the intestines, studies are reporting that there are genomic links between Fusobacterium nucleatum/necrophorum found in most acute appendicitis and the development of inammatory bowel disease and subsequent colorectal cancer [12, 64].
There are many studies on whether PA is cost- effective or not. In studies conducted, it has been reported that incidental appendectomies and pro­phylactic appendectomies performed before the age of 30 have a positive and cost-effective contribution [65]. The operation must be performed with mini­mal complications. Twenty years after a PA, a case with ileus and intestinal necrosis due to regional adhesions has been reported in the literature [14].
17.5 Conclusion
Prophylactic or incidental appendectomy can ethically be performed with minor complica­tions. PA should be recommended in patients without comorbidity and at a younger age (<30). IA should be performed in patients who are con­sidered to have no adverse effects on morbidity and mortality and thought that IA would be ben­ecial. The surgery decision must be made with the patient and family. In addition to preventing future appendicitis and associated complications, PA will also assist in the early diagnosis of appen­dix malignancies.
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Vascular Problems Related toColectomy: Habitual andVariant Anatomy, Prevention, andTactical Aspects
AbeFingerhut , HayatoKurihara , andWilliamTzu-LiangChen
18
18.1 Introduction
While the normal vascular anatomy of the colon and rectum is well documented [1, 2], variations are highly prevalent and may be an underlying cause of vascular failure after colonic resection and anastomosis. Indeed, adequate oxygen sup­ply is mandatory for the normal healing process [35]. Insufcient blood supply, with its obvious corollary, insufcient oxygen supply to the site of healing (anastomosis), and thus a risk factor for anastomotic breakdown, can be secondary to inadvertent division (whether the vessel is in its “normal” situation, or not), stretching or twisting of the alimentary vessels of one of the enteric segments, or division of vessels as necessary to perform a procedure (high or low tie of the infe-
A. Fingerhut (*) Department of Surgery, Section for Surgical Research, Medical University of Graz, Graz, Austria
Department of General Surgery, School of Medicine, Shanghai Minimally Invasive Surgery Center, Ruijin Hospital, Shanghai Jiao Tong University, Shanghai, People’s Republic of China e-mail: abengerhut@aol.com
H. Kurihara Istituto Clinico Humanitas, Emergency Surgery and Trauma Section, General and Minimally Invasive Surgery, Rozzano (Milan), Italy e-mail: hayato.kurihara@humanitas.it
W. T.-L. Chen Department of Colorectal Surgery, China Medical University Hsinchu Hospital, Hsinchu, Taiwan e-mail: wtchen@mail.cmuh.org.tw
rior mesenteric artery with its corollar interrup­tion of the left colic artery), especially when there is an insufcient anastomotic arc between the superior and inferior mesenteric circulations at the level of the marginal artery (of Drummond) or Grifths’ point, absence of the middle colic artery (MCA) or one of its branches, and last, but not least, when vascular supply to the colon does not take its normal course, notably when athero­sclerosis or previous colectomy obstructs or interrupts the normal vascularization.
Moreover, several anatomic regions along the gastrointestinal tract are known to have a tenuous vascular supply and after dissection and division of adjacent vessels, the gastrointestinal segment can become hypo-perfused, or even ischemic. This is the case when small hypoplastic vessels are present, notably at the level of Grifths’ point [6]. Ischemia of the intestinal segment to be anas­tomosed can also be due to inadvertent ligation of terminal vessels supplying the edges, incorrect angle of division, or too generous trimming of the mesenteric border [7].
In this chapter we will review the most com­monly encountered vascular patterns and their variations, highlighting how these variants may inuence the vascular supply to the remaining colorectal structure during the most commonly performed colorectal resections and the conse­quences for the surgeon performing colorectal surgery.
© The Author(s), under exclusive license to Springer Nature Switzerland AG 2021 O. N. Dilek et al. (eds.), Prophylactic Surgery, https://doi.org/10.1007/978-3-030-66853-2_18
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A. Fingerhut et al.
18.2 Normal (Traditional) Anatomy
The most prevalent vascularization (approxi­mately one-third of the population) of the terminal ileum, colon, and rectum (main organs involved in colorectal surgery) relies on vascular supply from the superior and inferior mesenteric arteries (SMA and IMA, respectively). The SMA runs off the aorta opposite L1 and supplies blood to the termi­nal ileum, the cecum, the ascending colon, and the proximal half to two-thirds of the transverse colon by the main branches of the SMA (the middle colic, the inconsistent right colic (less than 50%), the ileocolic arteries and the terminal branches of the SMA) [8]. The IMA runs off the aorta at the level of L3 and supplies blood to left half to left third of the transverse colon, the descending, the sigmoid colon and the upper third of the rectum by its main branches, namely the left colic, the sig­moid and the terminal, upper rectal artery.
18.2.1 Branches oftheSMA
The MCA, usually the second branch of the SMA (after the inferior pancreaticoduodenal artery), normally gives rise to two branches, a right (rela­tive to the patient) branch that anastomoses with
the right colic (when present) or the ascending branch of the ileocolic terminal division, and a left (relative to the patient) branch that anastomo­ses with the ascending or right divisional branch of the left colic artery, forming Drummond’s arcade or anastomosis, also called the peripheral arterial arcade [9] (Fig.18.1).
The watershed of marginal blood ow between the SMA and IMA lies somewhere near the splenic exure and has been called the Grifths’ point [6,
9] (circle in Fig. 18.1). Of note, this watershed
anastomosis can be absent or insufcient in up to 40% of patients. The marginal artery of Drummond is absent in 5% of patients or can sometimes either be replaced or complemented by other arcades such as the so-called Riolan or the meandering artery of Moskowitz, often when Grifths’ point is absent or insufcient. These complementary con­nections are called the proximal mesenteric arcades. Likewise, there is another critical second­ary watershed area between the vascular supply coming from the most distal sigmoid artery and the most proximal branch of the superior rectal artery called Sudeck’s critical point [9] (dotted circle in Fig. 18.1). This anastomosis is insuf­cient or absent in up to 15% of patients.
The right colic artery, when present, gives rise to two pericolic marginal branches, one ascend­ing, connecting with the right branch of the
Fig. 18.1 Normal colonic vascularization [9]. Grifths’ (full circle) and Sudeck’s (dotted circle) points are critical watershed vascular connections that warrant attention during colonic resection: (a) middle colic artery; (b) right colic artery; (c) ascending branch of the ileocolic artery; (d) left colic artery; (e) sigmoid arteries; (f) superior rectal artery; full circle: Grifths’ point (no vascular connection in up to 53% of patients); dotted circle: Sudeck’s critical point (no vascular connection in up to 15% of cases)
a
b
c
d
e
f
Right external
n
18 Vascular Problems Related to Colectomy: Habitual and Variant Anatomy, Prevention, and Tactical…
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MCA, the other descending, connecting to the ascending branch of the ileocolic artery.
The ileocolic artery divides into an ascending branch that irrigates the cecum and appendix, and anastomoses with the right branch of the middle colic or right colic artery and a descending branch that goes to the terminal ileum.
18.2.2 Venous Circulation
Right colon: Normally all arteries have their nominal venous counterparts (middle colic vein, right colic vein (more consistent than its arterial equivalent), ileocolic vein). While the ileocolic veins usually drain directly into the superior mes­enteric vein, the middle colic and right colic veins drain into a common trunk called the Henle trunk that usually runs directly into the superior mesenteric vein [8] (Fig.18.2).
Left colon: Normally all nominal venous counterparts (left colic vein, sigmoid veins, and superior rectal vein) drain directly into the infe­rior mesenteric vein (Fig.18.2).
18.2.3 Most Frequent Variants
Variations can be due to different congenital or acquired anatomic congurations (after colec­tomy, gastrectomy, pancreatic resection, or some­times even radical nephrectomy) or changes induced by chemo/radiation therapy or disease (atherosclerosis).
The MCA can be completely absent (25%) [7,
11], the two branches can arise directly from the
SMA (without a common trunk), one or the other can be absent, or there is no communication between the two branches (5–10%) (Fig.18.3). The right colic artery is absent in up to 1/3 of cases. The communication between the SMA and IMA at the splenic exure (Grifths’ point con­nection) can be absent or inadequate in 43 to 53% of cases [6, 1214].
The ileocolic artery can pass in front of (30%), or behind (60%) the superior mesenteric vessels (Fig.18.3) [15]. This has its importance when lymph node dissection of the origin of the ileocolic vessels is envisioned, nota­bly in complete mesocolic excision.
Fig. 18.2 Right and left colonic venous networks [10]
Portal vein
Superior mesenteric vein
Right colic
vein
IIeocolic vein
Common
iliac vein
iliac vein
Internal
iliac vein
Middle rectal vein
Inferior rectal vein
Splenic vein
Inferior mesenteric vein
Left colic vei
Sigmoid vein
Middle sacral vein
Superior rectal vein
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