Systematic Reviews Open Access
Copyright ©The Author(s) 2021. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Gastrointest Surg. Jul 27, 2021; 13(7): 702-716
Published online Jul 27, 2021. doi: 10.4240/wjgs.v13.i7.702
Acute mesenteric ischemia and small bowel imaging findings in COVID-19: A comprehensive review of the literature
Lorena Pirola, Andrea Palermo, Giacomo Mulinacci, Laura Ratti, Maria Fichera, Pietro Invernizzi, Chiara Viganò, Sara Massironi, Division of Gastroenterology and Center for Autoimmune Liver Diseases, Department of Medicine and Surgery, University of Milano-Bicocca, Monza 20900, Italy
Lorena Pirola, Andrea Palermo, Giacomo Mulinacci, Laura Ratti, Maria Fichera, Pietro Invernizzi, Chiara Viganò, Sara Massironi, European Reference Network on Hepatological Diseases, San Gerardo Hospital, Monza 20900, Italy
ORCID number: Lorena Pirola (0000-0002-9652-1614); Andrea Palermo (0000-0001-8057-9398); Giacomo Mulinacci (0000-0002-9398-893X); Laura Ratti (0000-0003-0198-6433); Maria Fichera (0000-0002-5787-1371); Pietro Invernizzi (0000-0003-3262-1998); Chiara Viganò (0000-0003-3401-1421); Sara Massironi (0000-0003-3214-8192).
Author contributions: Pirola L and Viganò C planned the work; Pirola L, Viganò C and Massironi S contributed to the design and conceptualization of the study; Palermo A and Mulinacci G wrote the first draft of the manuscript and edited the figures and tables; Pirola L, Ratti L, Fichera M and Viganò C edited the subsequent versions of the manuscript; Viganò C and Massironi S revised the manuscript for relevant intellectual content; Invernizzi P corrected the final version; all the authors read and approved the final version of the manuscript.
Conflict-of-interest statement: The authors declare that they have no competing interests.
PRISMA 2009 Checklist statement: The authors have read the PRISMA 2009 Checklist, and the manuscript was prepared and revised according to the PRISMA 2009 Checklist.
Open-Access: This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/Licenses/by-nc/4.0/
Corresponding author: Chiara Viganò, MD, Doctor, Division of Gastroenterology and Center for Autoimmune Liver Diseases, Department of Medicine and Surgery, University of Milano-Bicocca, Via Pergolesi 33, Monza 20900, Italy. c.vigano@hotmail.it
Received: February 8, 2021
Peer-review started: February 8, 2021
First decision: March 30, 2021
Revised: April 12, 2021
Accepted: July 2, 2021
Article in press: July 2, 2021
Published online: July 27, 2021

Abstract
BACKGROUND

Coronavirus disease 2019 (COVID-19), an infectious condition caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), has rapidly spread worldwide since its first description in Wuhan in December 2019. Even though respiratory manifestations are the most prevalent and responsible for disease morbidity and mortality, extrapulmonary involvement has progressively gained relevance. In particular, gastrointestinal (GI) signs and symptoms, reported in up to two-thirds of patients with COVID-19, might represent the first and, in some cases, the only disease presentation. Their presence has been associated in some studies with an increased risk of a severe disease course. Proposed pathogenic mechanisms explaining GI tract involvement are either direct viral access to intestinal cells via angiotensin-converting enzyme 2 or indirect damage of the intestinal wall through mesenteric ischemia induced by the hypercoagulable state associated with COVID-19 infection. Although not typical of SARS-CoV-2 infection, several small bowel manifestations have been described in infected patients who underwent any form of abdominal imaging. The radiological findings were mainly reported in patients with abdominal symptoms, among which abdominal pain was the most common.

AIM

To discuss small bowel radiological manifestations of SARS-CoV-2 infection in abdominal imaging studies.

METHODS

Bibliographical searches were performed in PubMed, using the following keywords: “COVID-19” AND “imaging” AND “gastrointestinal” OR “abdominal” OR “small bowel”.

RESULTS

Of 62 patients with described radiologic small bowel alterations, mesenteric ischemia was diagnosed in 31 cases (50%), small bowel wall thickening in 10 cases (16%), pneumatosis in nine cases (15%), intussusception in eight cases (13%), pneumoperitoneum in two cases (3%) and paralytic ileus in two cases (3%). We also reported mesenteric adipose tissue hypertrophy and lymph nodes enlargement in a young woman.

CONCLUSION

So far it is difficult to establish whether these manifestations are the direct consequence of SARS-CoV-2 infection or collateral findings in infected patients, but their recognition would be pivotal to set a closer follow-up and to reduce missed diagnoses.

Key Words: COVID-19, SARS-CoV-2, Radiology, Small intestine, Abdomen

Core Tip: Gastrointestinal manifestations of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection have been increasingly reported and corresponding abdominal imaging findings have been recognized. The present review includes case reports, case series, and retrospective studies discussing small bowel radiological manifestations of SARS-CoV-2 infection in abdominal imaging studies. Out of 62 patients, the most commonly reported finding was mesenteric ischemia, with a prevalence of 50%. Other less frequent features were small bowel wall thickening (16%), pneumatosis intestinalis (15%), intussusception (13%), pneumoperitoneum (3%), and paralytic ileus (3%). We also report a patient with mesenteric adipose tissue hypertrophy and lymph node enlargement.



INTRODUCTION

Coronavirus disease 2019 (COVID-19) is an infectious condition caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), firstly isolated in December 2019 in Wuhan, China[1]. As of February 8, 2021, there have been more than one hundred million confirmed cases of COVID-19, with more than two million deaths[2]. The most common COVID-19 symptoms include fever (85.6%), cough (65.7%), fatigue (42.4%) and dyspnea (21.4%)[3]. Although respiratory tract manifestations are the most prevalent and responsible for disease morbidity and mortality, extrapulmonary involvement has progressively gained relevance. In particular, gastrointestinal (GI) symptoms are described in a significant proportion of infected patients, being reported in up to two-thirds of patients with COVID-19[4]. Several studies suggest that GI symptoms might not only be the initial presentation of SARS-CoV-2 infection but are also the only manifestation reported during disease course in about 10% of cases[5]. Patients presenting with GI manifestations alone have a delayed diagnosis[6]. Furthermore, in some studies the presence of GI symptoms has been associated with an increased risk of severe clinical course, but the real impact of GI involvement on disease outcome is still a matter of debate[6,7]. The most commonly reported GI symptoms were loss of appetite (21%), diarrhea (9%), nausea or vomiting (6%), and abdominal pain (3%)[6]. It has been widely described and accepted in the literature that SARS-CoV-2 exploits angiotensin-converting enzyme 2 (ACE2) to gain access to single cells[8]. Hence, it is possible to assume that cells with higher expression of ACE2, such as enterocytes in the GI tract[9], are more susceptible to infection[10]. Several reports have evaluated the pulmonary radiological findings in COVID-19, which facilitate disease recognition and add to the understanding of its pathogenic mechanisms in the lung[11]. However, despite the broad spectrum and the high prevalence of GI symptoms, only a few studies have assessed the abdominal radiological findings in COVID-19 patients, and only a few of those have focused on small bowel alterations. Furthermore, the pathogenic mechanisms behind the described findings remain unclear, highlighting the importance of collecting further evidence on the topic. In this review, we analyzed the radiological small bowel findings in patients with COVID-19 and evaluated their impact on the whole clinical picture of the disease.

MATERIALS AND METHODS

Bibliographical searches were performed in PubMed, using the keywords “COVID-19” AND “imaging” AND “gastrointestinal” OR “abdominal” OR “small bowel”. PubMed was used to search for all relevant articles published since the first description of SARS-CoV-2 infection, which occurred in December 2019, until the end of January 2021. Reference lists from studies selected from the electronic search were manually searched to identify further relevant reports. Reference lists from all available review articles, primary studies, and proceedings of major meetings were also considered. Articles published as abstracts were included. Only English-language papers were included.

RESULTS

Thirty-nine articles describing small bowel imaging findings in patients with COVID-19 were identified. The review included 28 case reports, six case series, and five retrospective studies discussing radiological manifestations of SARS-CoV-2 infection in abdominal imaging studies. Several small bowel radiological manifestations have been described in infected patients, with a prevalence ranging from 3% to 21%[12,13]. They were mainly reported in patients with abdominal symptoms, among which abdominal pain was the most common. Of the 62 patients with small bowel radiological findings, acute mesenteric ischemia (AMI) was the most prevalent condition, diagnosed in 31 cases (50%). The characteristics of COVID-19 patients with AMI are shown in Table 1. Other radiological findings (Figure 1) were small bowel wall thickening in 10 cases (16%), pneumatosis in nine (15%), intussusception in eight (13%), pneumoperitoneum in two (3%), and paralytic ileus in two (3%). A summary of those findings is shown in Table 2. In addition, we reported mesenteric adipose tissue hypertrophy and lymph node enlargement in a young woman.

Figure 1
Figure 1 Proportions of radiologic small bowel manifestations reported since the beginning of the severe acute respiratory syndrome coronavirus 2 pandemic.
Table 1 Clinical characteristics and radiological findings of acute mesenteric ischemia in coronavirus disease-2019 patients.
Ref.
Patients, n
Age in yr
Gender
GI symptoms
Respiratory symptoms
Relevant laboratory test
Imaging modality
Radiological findings
Treatment
Outcome
de Barry et al[17]179FAbdominal pain, diarrheaYesWBC 12.6 × 109/L; CRP 125 mg/LCTMesenteric ischemia; upper mesenteric vein and portal thrombosis; upper mesenteric artery and jejunal artery thrombosisLaparotomy with segmental resection; thrombolysis and thrombectomyDead 4 d after surgery
Beccara et al[18]152MAbdominal pain, diarrhea, vomitingYesWBC 30 × 109/L; CRP 222 mg/LCTMesenteric ischemia; upper mesenteric artery thrombosisLaparotomy with segmental resection; anticoagulant; antiaggregantNR
Ofosu et al[19]155MNRYesWBC 9.5 × 109/L; CRP 3 mg/L; D-dimer 440 ng/mLCTMesenteric ischemia; portal vein thrombosisAnticoagulantDischarged
La Mura et al[20]172MNRNoWBC 19.76 × 109/L (n 81%); CRP 172.3 mg/LCTMesenteric ischemia; portal vein thrombosisAnticoagulantDischarged
Del Hoyo et al[21]161FAbdominal pain, vomitingNoCRP 9.43 mg/L; D-dimer 43.998 ng/mLCTMesenteric ischemia; spleen-portal vein and hepatic vein thrombosisAnticoagulantDead
Karna et al[22]161FAbdominal pain, distensionYesNRCTMesenteric ischemia; upper mesenteric artery thrombosisLaparotomy with segmental resection; anticoagulant; antiaggregantDead 36 h after surgery
Cheung et al[23]155MAbdominal pain, diarrhea, nauseaNRNRCTMesenteric ischemia; upper mesenteric artery thrombosisNRNR
de Roquetaillade et al[24]1NRNRNRNRNRCTMesenteric ischemiaNRNR
Vartanoglu et al[25]5NRMNRYesWBC 8.67 × 109/L (mean); CRP 970 mg/L (mean); D-dimer 447 ng/mL (mean); Fib 6245 mg/dL (mean)NRMesenteric ischemiaNR1 patient dead
Fraissé et al[26]3NRNRNRNRNRNRMesenteric ischemiaNRNR
Ignat et al[27]128FAbdominal pain, vomitingNoNRCTMesenteric ischemia; upper mesenteric vein and portal vein thrombosisLaparotomy with segmental resectionNR
Pang et al[28]130MAbdominal pain, vomitingNoD-dimer 20000 ng/mL; Fib 465 mg/dLCTMesenteric ischemia; upper mesenteric vein thrombosisLaparotomy with segmental resection; anticoagulantDischarged
Bianco et al[29]159MAbdominal pain, nauseaYesNRCTMesenteric ischemia; peritoneal free fluidLaparotomy with segmental resectionDead 4 d after surgery
Norsa et al[30]379FAbdominal painNRD-dimer 8 × ULNCTMesenteric ischemiaNRNR
62MAbdominal pain, vomitingNRD-dimer 76 × ULNCTMesenteric ischemia; upper mesenteric vein thrombosisNRDead
83FAbdominal painNRD-dimer 3 × ULNCTMesenteric ischemiaNRDead
Collange et al[31]156MNRNRD-dimer 2260 ng/mL; Fib 113 mg/dLCTMesenteric ischemia; mesenteric intravenous airLaparotomy with segmental resection; anticoagulantNR
Vulliamy et al[32]175MAbdominal pain, vomitingYesWBC 18 × 109/L; D-dimer 32000 ng/mLCTMesenteric ischemia; embolic occlusion of upper mesenteric arteryLaparotomy with segmental resection; thrombectomyNR
Rodriguez-Nakamura et al[33]245MAbdominal painYesWBC 16.6 × 109/L (n 86%); CRP 367 mg/L; D-dimer 1450 ng/mL; Fib 579 mg/dLCTMesenteric ischemia; upper mesenteric thrombosisLaparotomy with segmental resection; anticoagulantDischarged
42FAbdominal painYesWBC 18.8 × 109/L (n 83.5%); CRP 239 mg/L; D-dimer 14.407 ng/mL; Fib 338 mg/dLCTMesenteric ischemia; mesenteric veins and portal vein thrombosisLaparotomy with segmental resectionDead 48 h after surgery
E English et al[34]140MAbdominal distensionYesFib 548 mg/dLCTMesenteric ischemiaLaparotomy and laparoscopy with segmental resectionDead 48 h after surgery
Helms et al[35]1NRNRNRNRNRCTMesenteric ischemiaNRNR
Mitchell et al[36]169MAbdominal pain, constipation, eructationNRNRCTMesenteric ischemia; upper mesenteric artery thrombosisLaparotomy with segmental resection; thrombolysis and thrombectomyDischarged
Azouz et al[37]156MAbdominal pain, vomitingNoNRCTMesenteric ischemia; upper mesenteric thrombosisLaparotomy with segmental resection; anticoagulantNR
Franco-Moreno et al[38]127MAbdominal painYesWBC 18 × 109/L (n 85%); CRP 245 mg/L; D-dimer 9530 ng/mL; Fib > 500 mg/dLCTMesenteric ischemia; portal vein thrombosisAnticoagulantDischarged
Table 2 Other small bowel radiological findings in coronavirus disease-2019 patients and relevant clinical characteristics.
Ref.
Patients, n
Age in yr
Gender
GI symptoms
Imaging modality
Radiological findings
Other relevant information
Hellinger et al[40]164NRAbdominal pain, nausea, vomiting, diarrhea, feverCTSmall bowel thickening and hyperemia-
Bhayana et al[12]518-99NRAbdominal pain, nausea, vomiting, diarrhea, feverCTSmall bowel thickening100% of patients needed ICU
Goldberg-Stein et al[13]2NRNRNRCTSmall bowel thickening-
Periyakaruppan et al[41]1NRMAbdominal pain, diarrheaCTSmall bowel thickeningComplete recovery after 2 d from I.V. immunoglobulin infusion
Guo et al[42]129MDiarrhea, feverCTSmall bowel thickening-
Bhayana et al[12]418-99NRAbdominal pain, nausea, vomiting, diarrhea, feverCTPneumatosis intestinalis20% of patients needed ICU.100% of patients underwent laparotomy
Tirumani et al[48]1NRNRNRCTPneumatosis intestinalis; portal venous gas-
Kielty et al[49]147MVomitingCTPneumatosis intestinalis; peritoneal free fluidThe patient needed ICU. No need of surgery. Discharged
Di Grezia et al[50]3NRNRNRCTPneumatosis intestinalisNeeded surgical intervention with open abdomen and negative pressure therapy (no need of intestinal resection)
Makrinioti et al[54]210-moFCrying, vomiting, red currant jelly-like stoolUSIleocolic intussusceptionDead
10-moFBilious vomiting, red currant jelly-like stoolNRIntussusceptionRecovered after surgery
Rajalakshmi et al[55]18-moMVomiting, blood-stained stoolsUSIntussusceptionRecovered after surgery
Moazzam et al[56]14-moMAbdominal painUSIntussusception with "doughnut sign"Recovered after surgery
Bazuaye-Ekwuyasi et al[57]19-moMAbdominal pain, vomiting, decreased oral intake, and blood-streaked stoolRXIntussusception with "target" signRecovered after surgery
US
Cai et al[58]110-moFVomiting, currant jelly-like stoolUSIntussusceptionDead
Martínez-Castaño et al[59]16-moMVomiting, abdominal cramps, currant jelly stoolsUSIleocolic intussusceptionDischarged
Lu et al[60]110-moNRNRNRIntussusceptionDead
AMI

AMI is a pathological condition characterized by a sudden decline in blood flow through the mesenteric vessels, resulting in a discrepancy between the metabolic need of the visceral organs and actual oxygen delivery[14]. If untreated, it may lead to small bowel wall necrosis, with a mortality rate of up to 80%[15]. Among the causes of AMI, the most prevalent are acute mesenteric artery embolism, nonocclusive mesenteric ischemia[16], and acute mesenteric vein thrombosis. So far, 22 papers have been published describing mesenteric ischemia in 31 COVID-19 patients, including 17 case reports, two case series, and three retrospective studies[17-38]. The characteristics and radiological findings of COVID-19 patients with AMI are reported in Table 1. All but one patient underwent abdominal contrast-enhanced computed tomography (CT) scan after the onset of GI symptoms such as nausea, vomiting, and/or abdominal pain. Among the vascular findings, the most frequent were nine cases with thrombosis of the upper mesenteric artery or jejunal artery and nine cases of thrombosis of splanchnic veins, of which seven involved the portal vein, five involved the superior mesenteric vein (Figure 2), and one involved splenic and hepatic veins. Other findings described in association with AMI were the presence of liquid in the peritoneal cavity (two cases), bowel distension (one case), mesenteric intravenous air (one case), and splenic infarction (one case). From a pathological perspective, it is of interest that none of the patients had evidence of a systemic atherosclerotic disorder or other pathologic conditions that could possibly explain the findings. Treatment of AMI was reported in 17 cases. Thirteen (76%) were treated by segmental resection of small bowel, and anticoagulant therapy alone was administered in four cases. Of the nineteen patients with a reported outcome, nine (47%) died.

Figure 2
Figure 2 Computed tomography image showing partial superior mesenteric vein thrombosis in a man with severe acute respiratory syndrome coronavirus 2 infection.
Small bowel wall thickening

Thickening of the small bowel wall may occur secondary to neoplastic, inflammatory, infectious, or ischemic conditions[39]. It was first described by Hellinger et al[40] in a patient presenting at the emergency room with abdominal symptoms, and this condition has been subsequently reported in other COVID-19 patients (Figure 3). At the time of writing, we identified five papers, three case reports and two retrospective studies, describing ten patients with radiological evidence of small bowel wall thickening. In a study of 412 patients admitted to the hospital for SARS-CoV-2 infection, 42 underwent abdominal CT scans. In five of those patients (11.9%) small bowel thickening, reported as a single-wall thickness greater than 3 mm in distended loops or greater than 5 mm in collapsed loops[12], was described. In a report including 141 COVID-19 patients who underwent abdominopelvic CT within 14 d of diagnosis, GoldbergStein et al[13] reported a small bowel thickening prevalence of 2.5%. In addition, diffuse mural wall thickening of the ileum was reported in a single case study of a 11-year-old boy with SARS-CoV-2 infection, who presented to the emergency room with fever, diarrhea, and abdominal pain, without respiratory symptoms[41]. Lastly, Guo et al[42] described segmental wall thickening involving a segment of jejunum in a 29-year-old man presenting with diarrhea and fever. The cause of small bowel thickening in SARS-CoV-2 infected patients is still unclear. It may be a manifestation of local inflammation and edema secondary to direct or indirect viral damage of the bowel wall. Another hypothesis is that may be linked to hypercoagulability secondary to viral infection, which may promote formation of fibrin clots in the microcirculation, leading to ischemia and edema.

Figure 3
Figure 3 Magnetic resonance image showing distal ileum wall thickening in a young woman with severe acute respiratory syndrome coronavirus 2 infection.
Pneumatosis intestinalis

Pneumatosis intestinalis is a radiological sign reflecting the presence of gas within the intestinal wall, most commonly in the mucosa or submucosa. Pneumatosis can occur in any part of the digestive tract, and may even be accompanied by the presence of gas in the portal or mesenteric vein[43]. The clinical relevance of pneumatosis intestinalis varies widely and ranges from a benign to life-threatening condition depending on the underlying cause[44]. This pathologic finding has been previously described in association with viral infections, such as cytomegalovirus, adenovirus, rotavirus, and norovirus, and the proposed pathogenic mechanism was direct mucosal damage caused by viral activity[44-47].

So far, four papers, one case report, one case series, and two retrospective studies, have described pneumatosis intestinalis in nine patients with SARS-CoV-2 infection. Bhayana et al[12] described pneumatosis intestinalis of the small bowel in four of 42 COVID-19 patients (9.5%) with abdominal CT scans. The percentage reached 20% in patients admitted to the intensive care unit. All patients underwent laparotomic exploration. Two cases showed frank signs of bowel necrosis, with bowel resection performed in one. Fibrin clots were detected in arterioles adjacent to the necrotic mucosa in histological samples. In a retrospective study, Tirumani et al[48] described small bowel pneumatosis with portal venous gas in one of 73 SARS-CoV-2 infected patients with abdominal CT scans. Pneumatosis intestinalis of the small bowel was also reported in a small study of three cases and in a single-patient case report. Complete resolution was reported following conservative treatment in a patient with widespread pneumatosis affecting the jejunum, proximal ileum, and caecum, for which surgery was deemed to be associated with unacceptably high morbidity[49]. In the remaining three patients, an open abdomen with negative pressure therapy was successfully performed without the need of intestinal resection[50]. The rationale behind this approach lies in the capability of either increasing gastrointestinal arterial and venous blood flow through intra-abdominal pressure reduction and dampening intestinal cytokine release in the peritoneal cavity, which might also prevent the deterioration of lung function[12,51,52].

Intussusception

Intussusception is the invagination of a segment of the bowel within a more distal one[53]. It is the most common cause of bowel obstruction in infants, usually occurring between 4 and 10 mo of age[53]. On the contrary, intussusception in adults is a rare disease, accounting for less than 5% of bowel obstruction episodes[53]. In both children and adults, intussusception usually involves the ileum, with ileocecal valve invagination into the cecum being the most common localization. Furthermore, 90% of cases of intussusception in adults are secondary to a well-defined pathological condition, such as inflammatory bowel disease, postoperative tractions, Meckel’s diverticulum, benign and malignant lesions, metastatic neoplasms, or even an iatrogenic cause (e.g., intestinal tubes, jejunostomy feeding tubes, or gastric surgery)[53]. Conversely, in the pediatric age group, approximately 90% of cases are idiopathic. In the literature, viral infection was cited as a possible cause of intussusception in children[54]. Indeed, local immune activation and mesenteric adenitis may trigger enhanced peristaltic activity, consequently leading to the invagination of the proximal bowel segment into the distal one[54].

So far, eight cases of intussusception were reported in children between 4 and 10 mo of age with laboratory-confirmed SARS-CoV-2 infection in one case series, five case reports, and one retrospective study[54-60]. The diagnosis was made mainly by ultrasound (US) through the presence of typical findings of intussusception, such as the doughnut sign (i.e. concentric alternating hyperechoic and hypoechoic rings); as expected, in all cases except one in which the site of intussusception was not specified, the ileocolic tract was involved. Three patients died of complications. To date, it has not been possible to establish an association between SARS-CoV-2 infection and intussusception. Testing for viral pathogens, including SARS-CoV-2, may be considered in infants with symptoms consistent with intussusception or with typical radiological findings.

Small bowel perforation

Pneumoperitoneum, an indirect sign of small bowel perforation, refers to the presence of free air in the abdominal cavity, often suspected through abdominal radiography and confirmed on CT scans[61]. It has been less frequently reported than the previously mentioned radiologic features. One case report and one retrospective study described small bowel perforations in two patients with SARS-CoV-2 infection without any other possible explanation other than viral infection. Both cases were then confirmed by laparoscopic exploration[12,62]. The clinical outcome was not specified in one study. In the other, despite prompt orotracheal-intubation and surgery, the patient developed refractory septic shock and died[12,62]. As for the previously described findings, the disease pathogenesis is unknown. However, it is likely that small bowel perforation occurred as a consequence of either viral action on the intestinal mucosa or as a consequence of ischemic small bowel necrosis.

Paralytic ileus

Paralytic ileus is defined as a temporary functional cessation of propulsive contractions of the gastrointestinal tract, with subsequent upstream gut dilation and accumulation of secretions and gas within the lumen[63]. Diagnosis of paralytic ileus is established by the coexistence of a clinical suspect and the support of radiological imaging. Many conditions may cause paralytic ileus, the most common being abdominal or retroperitoneal surgery. Other causes include the use of opioids, intra-abdominal infections, bleeding, hypokalemia, and the absence of enteral nutrition[64]. In patients with SARS-CoV-2 infection, one case of paralytic ileus of the small bowel was reported in a retrospective study, and another, involving both the small and the large bowel was described in a case report[13,65].

Mesenteric adipose tissue hypertrophy and enlarged lymph nodes

Even though there are very few data available in literature at the time of writing, small bowel involvement in SARS-CoV-2 infection may also lead to mesenteric activation and lymph nodes enlargement[66]. We report those alterations in a 34-year-old woman with SARS-CoV-2 infection presenting abdominal pain, vomiting, and diarrhea. Abdominal US showed enlarged abdominal lymph nodes with a maximum short-axis diameter of 17 mm, and mesenteric adipose tissue hypertrophy (Figure 4). Abdominal CT confirmed the presence of multiple mesenteric enlarged lymph nodes associated with adipose tissue hypertrophy (Figure 5).

Figure 4
Figure 4 Abdominal ultrasound image in a 34-year-old woman with severe acute respiratory syndrome coronavirus 2 infection. Enlarged hypoechoic mesenteric lymph nodes, with a maximum longitudinal axis diameter of 17 mm (arrow, A) and hyperechoic mesenteric adipose tissue hypertrophy (arrow, B) are shown.
Figure 5
Figure 5 Abdominal computed tomography image showing multiple enlarged lymph nodes and mesenteric adipose tissue hypertrophy in a 34-year-old woman with severe acute respiratory syndrome coronavirus 2 infection.
DISCUSSION

In this review, we focused on the small bowel radiological findings in COVID-19 patients, as described so far mainly in patients presenting with GI symptoms. Although no specific aspect was identified, some radiological features have been reported in a significant proportion of patients with GI symptoms, reaching up to 21% of prevalence. Among them, AMI was the most frequent. AMI is an uncommon cause of abdominal pain, accounting for 0.09%-0.2% of all acute surgical admissions to emergency departments[15]. Acute mesenteric arterial embolism caused by atrial fibrillation, thrombosis of the superior mesenteric artery (SMA) in a background of pre-existing chronic atherosclerotic disease, and nonocclusive mesenteric ischemia secondary to SMA vasoconstriction, are the major causes of AMI. Hypercoagulability, including that induced by inherited disorders such as Factor V Leiden and prothrombin mutations, protein S and C deficiency, and others, promote mesenteric venous thrombosis and have been described as causative agents of AMI[15].

Interestingly, enteric involvement has been described in other beta coronavirus infections such as SARS and Middle East respiratory syndrome, but a strong relationship with AMI has never been reported. Of note, all cases of AMI reported during COVID-19 infection were subsequent to direct vascular obstruction, thus ruling out the possibility of nonocclusive mesenteric ischemia[67,68]. It has been widely reported that SARS-CoV-2 infection is associated with an increased risk of various thromboembolic complications[69]. Indeed, SARS-CoV-2 infection induces a hypercoagulable state through systemic inflammation, endothelial activation, and hypoxia. The tropism of SARS-CoV-2 for the vascular endothelium may be explained by the expression of the ACE2, the target receptor for viral entry into cells, and endothelial damage induces massive release of Von Willebrand factor, further increasing the risk of thrombosis[70]. Overall, both hemodynamic alterations consequent to vascular thrombosis and direct enterocyte damage might contribute to the development of small bowel ischemia and necrosis[70], although their exact contribution to the development of wall ischemia is still to be determined. Studies of histological samples are required to further explain the pathophysiology behind this manifestation. The mortality rate of AMI in COVID-19 is still unknown, yet it is likely to contribute significantly to an increased burden of disease. It is thus of the utmost importance to raise awareness among clinicians to recognize the typical signs of mesenteric ischemia, as early diagnosis and timely intervention are essential to decrease the mortality curve. Jung et al[71] recently described the role of contrast-enhanced ultrasonography (CEUS) to detect abdominal microcirculatory disorders in severe cases of COVID-19. CEUS has good sensibility in detecting areas of reduced micro-vascularization, even in the early stages[71]. Small bowel wall thickening was reported in 16% of cases. The cause is still unclear, but it may be a manifestation of local inflammation and edema secondary to direct viral damage of the bowel wall. Pneumatosis intestinalis is a radiological finding described in 15% of cases. The etiology in patients with COVID-19 remains unclear. Direct viral mucosal damage, intestinal ischemia, or atrophy of the lymphoid follicles with secondary increased mucosal permeability[72] were considered as possible pathogenic mechanisms.

Other reported imaging findings include intussusception (13%), pneumoperitoneum (3%), and paralytic ileus (3%). We also reported mesenteric enlarged lymph nodes and mesenteric adipose tissue hypertrophy in a young woman with COVID-19. It is possible that, in addition to direct viral damage of enterocytes, SARS-CoV-2 infection could promote a local immune activation with cytokines release, leading to the described alterations[66].

This review has some limitations. First, it is mainly based on case series and few retrospective studies, thus the real prevalence of the reported radiological findings may actually be significantly higher, as only a proportion of patients with GI symptoms undergo imaging studies. Further investigation of abdominal imaging abnormalities in COVID-19 patients is a topic for future research, and could help to decrease missed diagnosis, encourage closer follow-up, and decrease morbidity and mortality.

CONCLUSION

So far, the small number of reported cases does not allow to conclusively ascribe these manifestations to the direct action of SARS-CoV-2; nevertheless, it is important to exclude this infection in the current diagnostic workup of patients presenting with gastrointestinal symptoms.

ARTICLE HIGHLIGHTS
Research background

Coronavirus disease 2019 (COVID-19) is an infectious disease with predominant respiratory symptoms. Yet extrapulmonary manifestations have been increasingly recognized in COVID-19 patients. In particular, gastrointestinal (GI) symptoms are reported in up to two-thirds of patients and might be the only manifestations in some cases.

Research motivation

Given the high prevalence of gastrointestinal involvement of COVID-19 and the unclear association with disease clinical outcome, we believe that it could be of interest to deeply investigate small bowel involvement in severe acute respiratory syndrome coronavirus 2 infection.

Research objectives

To analyze and to summarize small bowel radiological features described in COVID-19 patients, and possibly clarify their impact on the clinical management of COVID-19 patients presenting with GI symptoms.

Research methods

A literature search of the PubMed electronic database was conducted using the MeSH terms “COVID-19”, “imaging” and “gastrointestinal” or “abdominal” or “small bowel”. The search was limited to English-language papers. All available case reports, case series and retrospective studies between December 2019 and January 2021 were included.

Research results

AMI is the major radiological finding in COVID-19 patients with small bowel involvement (50%). Less common findings are thickening of the small bowel wall, pneumatosis intestinalis, intussusception, and paralytic ileus. Furthermore, we described a case of mesenteric adipose tissue hypertrophy and enlarged lymph nodes associated to COVID-19.

Research conclusions

Gastrointestinal involvement in COVID-19 patients is highly prevalent. The most frequent small bowel alteration is AMI, a condition associated with high mortality. Raised awareness and prompt identification of small bowel involvement in COVID 19-patients could be essential to improve clinical management and clinical outcome, mainly in case of AMI.

Research perspectives

Further investigation of abdominal imaging abnormalities in COVID-19 patients may be a topic for future research and could help in reducing missed diagnoses and benefit overall morbidity and mortality.

Footnotes

Manuscript source: Invited manuscript

Specialty type: Gastroenterology and hepatology

Country/Territory of origin: Italy

Peer-review report’s scientific quality classification

Grade A (Excellent): 0

Grade B (Very good): B, B, B, B

Grade C (Good): 0

Grade D (Fair): D

Grade E (Poor): 0

P-Reviewer: de Melo FF, Sabelnikova EA, Shivaji UN S-Editor: Zhang H L-Editor: Filipodia P-Editor: Li JH

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