Literature DB >> 35433253

Spontaneous resolution of intussusception after COVID-19 infection found at laparoscopy in a 6-year-old.

Renato Díaz-Ruiz1,2, Paula Ponce-de-León-Lovatón3, Paulo Delgado-Seminario1, Diego Urrunaga-Pastor4.   

Abstract

The incidence of intussusception is 2.5 per 1000 live births, and infants between 4 and 10 months of age represent the highest frequency peak. Cases of intussusception with acute COVID-19 infection have been reported in infants under one year of age and with one death associated with MIS-C. However, we have not found reports of intussusception in schoolchildren. We report the case of a 6-year-old male with two days of illness that began with a sensation of temperature rise, headache, abdominal pain, liquid stools with mucus and no blood, hyporexia, chills, and food vomiting. He presented a negative result for the detection of SARS-CoV-2 antigen, negative SARS-CoV-2 IgM/IgG serology positive (lateral flow immunochromatography test), in addition to total IgM/IgG antibodies in 11.88 COI by means of a test of electrochemiluminescence. An abdominal ultrasound was performed that concluded invagination, for which an exploratory laparoscopy was performed and the patient evolved favorably. 13 cases of intussusception associated with acute COVID-19 infection have been described in this group. However, no reports of intussusception have been described after COVID-19 infection in school age. We recommend ruling out active or past SARS-CoV-2 infection in children with gastrointestinal symptoms and, if it exists, ruling out invagination by means of abdominal ultrasound.
© 2022 The Authors.

Entities:  

Keywords:  COVID-19; Child; Intussusception; Pediatric surgery; SARS-CoV-2

Year:  2022        PMID: 35433253      PMCID: PMC8994409          DOI: 10.1016/j.epsc.2022.102273

Source DB:  PubMed          Journal:  J Pediatr Surg Case Rep        ISSN: 2213-5766


Introduction

The incidence of intussusception is 2.5 per 1000 live births and infants between 4 and 10 months of age represent the maximum frequency peak [1] and it is considered the main cause of intestinal obstruction in infants [[2], [3], [4], [5], [6], [7], [8], [9]]. Although most are idiopathic [2,[6], [7], [8], [9], [10]], 30% are associated with previous viral infection [4,8] being the most common etiological factor [1,2,4]. Adenoviruses and rotaviruses represent 50% of cases associated with viral infection [[2], [3], [4], [5]], although poliovirus, enterovirus, parechovirus, and norovirus have also been found [4,8]. 6% of cases of intussusception are due to Meckel's diverticulum, Henoch- Schonlein purpura, intestinal duplication, polyp or lymphoma [8], with a precipitating lesion found in 10%–25% of cases [2]. 10% of children with COVID-19 present gastrointestinal symptoms [8] being more common than in adults [2,8]. It increases up to 18% in some reports [1] and manifests as abdominal pain, diarrhea and vomiting [3,4,6,10]. Cases of intussusception with acute COVID-19 infection have been reported in infants under one year of age and with one death associated with MIS-C [[1], [2], [3], [4], [5], [6], [7], [8], [9], [10], [11], [12]]. Although there are cases of intussusception in infants with active SARS-CoV-2 infection, we have not found reports of intussusception in schoolchildren who have presented the disease.

Case report

A 6-year-old male with two days of illness that began with a sensation of temperature rise, headache, and abdominal pain. Subsequently, liquid stools with mucus are added, without blood, hyporexia, chills and food vomiting. He goes to a private clinic where he is treated and discharged. The abdominal pain intensifies the next day, for which he returns to the private clinic, where laboratory tests are requested (Table 1 ), he is given treatment (not specified by relatives) and when the crampy pain in the mesogastrium and epigastrium increases, accompanied by feeling nauseous, they request voluntary withdrawal and come to our institution due to an emergency. Physical examination revealed pain on deep palpation in the mesogastrium. An abdominal ultrasound was performed that concluded intussusception, so surgical intervention was decided (Fig. 1 a).
Table 1

Summary of laboratory markers in the patient.

Diagnostic Aid ExamBefore Hospital AttentionPreoperative analysisPostoperative analysisAnalysis on the eighth postoperative day
PCR and/or VSGPCR 11.1 mg/dl (0–0.5)PCR 77.9 mg/l (0.01–5)VSG 15mm/h (1–10)PCR 38.5 mg/l (0.01–5)VSG 15mm/h (1–10)PCR 1.9 mg/l (0.01–5)
Urine and/or stool testRIH:>100 leukocytes/field8-10 red blood cells/fieldEx. Urine:Red blood cells 26–50/field (0–1)Hemoglobin 2+ albumin 1+Ketone bodies 2+Normal urineFunctional stool: positive thevenon
Complete blood countLeukocytes 13500 (5000–12000)Hb 13g/dlLymphocytes 25% (40–56)Leukocytes 11570 (4310–11000)Hb 11.1d/dlLymphocytes 21% (15.5–56.6)Platelets 522000 (206000–369000)Rest within normal
SARS CoV 2 DetectionSARS CoV 2 Antigen NegativeSARS CoV 2 serology IgM antibodies negativePositive IgG antibodiesTotal Ant IgM/IgG 11.88 COI (0–0.99)
Liver ProfileAlbumin 3.4g/dl (3.8–5.4)Proteins 5.7g/dl (6–8)Rest of normal liver profile
OthersCreatinkinase MB 3.5 ng/ml (0.3–4.87)Procalcitonin negativeTroponin T 0.001 ng/ml (0.001–0.014)Ferritin 131ng/ml (30–250)
Fig. 1

A: Abdominal ultrasound showing image of intussusception; B: Appendix without significant alteration and distal ileum not invaginated; C: mesenteric adenitis found during laparoscopic exploration; D: Liver with changes in its usual coloration.

Summary of laboratory markers in the patient. A: Abdominal ultrasound showing image of intussusception; B: Appendix without significant alteration and distal ileum not invaginated; C: mesenteric adenitis found during laparoscopic exploration; D: Liver with changes in its usual coloration. Preoperative tests (Table 1) show increased C-reactive protein (CRP), negative result for SARS-CoV-2 antigen detection, negative SARS-CoV-2 IgM/positive IgG serology (lateral flow immunochromatography test), in addition to total IgM/IgG antibodies in 11.88 COI by electrochemiluminescence test (normal value: 0.00–0.99). Urinalysis revealed albumin 1+, ketone bodies 2+, hemoglobin 2+, red blood cells 26–50/field (normal value: 0–1). The child's mother reported contact of the child with uncles who had a positive result for IgG in a lateral flow immunochromatography test, without having presented symptoms. During surgery, mesenteric adenitis, non-invaginated ileum, appendix without significant alterations and liver with change in color were observed (Fig. 1b, 1c and 1d). An appendectomy was performed using a laparoscopic technique and a postoperative liver profile was requested (Table 1). Given a presumptive diagnosis of MIS-C, the pediatrician requested laboratory tests (Table 1) and the cardiologist suggested continuing management by pediatric surgery. The patient evolved with mild and occasional pain, for which he was discharged on the second day after the operation, with analgesic. The patient came to the office 8 days after the operation and without symptoms. Control laboratory tests (Table 1) and echocardiography were taken, finding mild tricuspid regurgitation. In addition, the urinalysis did not present alterations, however, the functional coprology was positive for thevenon.

Discussion

The incidence of intussusception is 2.5 per 1000 live births, affecting infants in most cases [1]. 13 cases of intussusception associated with COVID-19 infection have been described in infants with a positive active infection test, although one of them had already been diagnosed with COVID-19 three weeks before the intussusception [9]. However, no reports of intussusception have been found after COVID-19 infection in school age. Most cases of intussusception occur in infants. This coincides with the cases of intussusception associated with COVID-19 infection, which mostly range between 4 and 10 months [1,2,[4], [5], [6], [7], [8],[10], [11], [12]]. However, cases have also been described in infants aged 2 months and 2.5 months [3,9]. We have not found cases in school-age children like the one we have presented who do not have an active SARS-CoV-2 infection. The generalized immune activation that exists during COVID-19 can cause hypertrophy of Peyer's patches [2], the virus binds to the angiotensin II converting enzyme and enters the cell of the intestinal tract, altering peristalsis and could cause invagination [8]. We believe that the mechanism by which our patient presented intussusception is the same as in the cases of infants reported to date, since despite being of school age, we did not find a mechanical cause, but we did find mesenteric adenitis. The clinical picture was characterized by intermittent colicky abdominal pain, hyporexia, fever, vomiting and liquid stools. Some of the symptoms were present in the previous cases and although our patient did not present bloody stools, red blood cells were found in the stools and urine before surgery. Most of the cases published to date do report the presence of bloody stools and some report palpation of an abdominal mass, which was not found in our patient (Table 2 ).
Table 2

Summary of previous clinical cases described in the literature.

AuthorAgeSexCOVID – 19 exposureDuration of symptomsFeverRespiratory SymptomsAbdominal SymptomsImage/type of intussusceptionTreatment and result
Díaz-Ruiz et al.6 yearsMYes2 daysYesNoAbdominal pain, vomiting, liquid stool, hyporexia. No palpable massUltrasound, ileocolicLaparoscopy, recovered
Bazuaye-Ekwuyasi et al. [2]9 monthsMYes6 daysYesYesAbdominal pain, dark stools No palpable massIleocolicHydrostatic reduction, recovered
Martínez-Castaño et al. [5]6 monthsMYes2 daysNoNoAbdominal pain, vomiting, bloody stools. No palpable massUltrasound, ileocecalHydrostatic reduction, recovered
Moazzam et al. [4]4 monthsMNo2 daysNoYesAbdominal pain, bloody stools. Finding of palpable massIleocecalPneumatic reduction, recovered
Cay et al. [2]10 monthsFNo1.25 daysYesNoVomiting, bloody stools. Does not specify palpable massX-ray, ultrasound, CT, does not specifyPneumatic reduction. Then laparotomy. Died.
Makrinioti et al. [11]10 monthsFYes2 weeksYesVomiting, bloody stools.UltrasoundFailed pneumatic reduction, then laparotomy. Recovered
Rajalakshmi et al. [12]8 monthsMNo2 daysYesNoVomiting, bloody stools. Finding of palpable massUltrasound ileocolicPneumatic reduction, recovered
Osorno et al. [1]8 monthsM3 daysYesAbdominal pain, bloody stools. Finding of palpable massUltrasound, ileocolicLaparotomy: ileostomy. Recovered
Athamnah et al. [3]2.5 monthsMMother with respiratory symptomsYesAbdominal pain, vomiting, bloating abdominal, bloody stoolsUltrasound, ileocolicPneumatic reduction, recovered
Noviello et al. [6]7 monthsMYes12 hoursNoAbdominal pain, hyporexia, vomiting, drowsiness, bloody stoolsUltrasound, ileocolicFailed nonsurgical treatment, then laparotomy (resection and anastomosis), recovered
Sullivan et al. [7]7 monthsM2 weeksIntermittent abdominal painUltrasound, ileocolicContrast enema reduction and discharge. Symptoms returns in the same way the next day, a CT scan is taken and ileoileal invagination is found. Resolved spontaneously and is discharged
Mercado-Martínez et al. [8]8 months7 monthsMF2 days1.5 daysYesYesNoYesVomiting, bloody stools. No palpable massAbdominal pain, bloody stools. Finding of palpable massUltrasound, ileocolicRadiography: dilated loops, air-fluid levels, no distal air.Laparotomy: manual reduction, recoveredLaparotomy: manual reduction, recovered
Khan et al. [9]2 monthsMNoCOVID-19, 3 weeks before illnessAbdominal pain, bloody stools, vomiting.IleocolicPneumatic reduction, recovered
Summary of previous clinical cases described in the literature. The image of choice to reach the diagnosis of intussusception is ultrasound. In most of the reported cases, ultrasound has also been used and in other cases, radiography and tomography. On the other hand, although the treatment of choice is non-surgical reduction, we opted for exploratory laparoscopy as it is a useful and valid diagnostic and treatment option with fewer complications than laparotomy. In addition, we did not have the necessary resources to do an emergency pneumatic or hydrostatic reduction. Most of the cases presented in the literature have been resolved non-surgical, others reached laparotomy after failure of non-surgical treatment, some performed laparotomy in the first instance and none attempted to resolve the case by laparoscopy.

Conclusion

In conclusion, in children with gastrointestinal symptoms, it is necessary to rule out an active or past COVID-19 infection and rule out the presence of associated invagination through ultrasound. If the diagnosis of intussusception is confirmed, laparoscopy offers a valuable method of treatment in our country, where resources such as ultrasound and/or fluoroscopy in emergency areas are not always available. Despite the limitation that exists in the diagnosis of COVID-19 through a lateral flow immunochromatography and electrochemiluminescence test, the epidemiological link of relatives with a positive lateral flow immunochromatography test increases the probability that they have asymptomatic Thus, we recommend ruling out past SARS-CoV-2 infection in children with intussusception.

Contributors

All the authors have participated in the conception and design of the article, data collection, writing, critical review of the article and approved the final version.

Funding

None.

Ethical approval and informed consent

We obtained the mother written informed consent to publish this clinical case including images and data reported.

Declaration of competing interest

The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.
  11 in total

1.  COVID-19 Infection Is a Diagnostic Challenge in Infants With Ileocecal Intussusception.

Authors:  Irene Martínez-Castaño; Elena Calabuig-Barbero; Jerónimo Gonzálvez-Piñera; José María López-Ayala
Journal:  Pediatr Emerg Care       Date:  2020-06       Impact factor: 1.454

2.  Novel Coronavirus Infection in an Infant with Intussusception.

Authors:  Juan Felipe Osorno; Manuel Giraldo; Andrés Felipe Marín; Luis Mauricio Figueroa
Journal:  Glob Pediatr Health       Date:  2021-05-08

3.  Intussusception and SARS-CoV-2 infection.

Authors:  Israel Mercado-Martínez; Francisco Javier Arreaga-Gutiérrez; Andrea Natalia Pedraza-Peña
Journal:  J Pediatr Surg Case Rep       Date:  2021-02-11

4.  COVID-19 presenting as intussusception in infants: A case report with literature review.

Authors:  Mohammad N Athamnah; Salim Masade; Hanady Hamdallah; Nasser Banikhaled; Wafa Shatnawi; Marwa Elmughrabi; Hussein S O Al Azzam
Journal:  J Pediatr Surg Case Rep       Date:  2021-01-07

Review 5.  Global Reports of Intussusception in Infants With SARS-CoV-2 Infection.

Authors:  Jennifer E Giovanni; Susan Hrapcak; Michael Melgar; Shana Godfred-Cato
Journal:  Pediatr Infect Dis J       Date:  2021-01       Impact factor: 3.806

6.  Intussusception in 2 Children With Severe Acute Respiratory Syndrome Coronavirus-2 Infection.

Authors:  Heidi Makrinioti; Alexander MacDonald; Xiaoxia Lu; Susan Wallace; Mathew Jobson; Furong Zhang; Jianbo Shao; Jonathan Bretherton; Tariq Mehmood; Elizabeth Eyre; Adelene Wong; Lorna Pakkiri; Amulya Saxena; Gary Wong
Journal:  J Pediatric Infect Dis Soc       Date:  2020-09-17       Impact factor: 3.164

Review 7.  COVID-19 Can Cause Severe Intussusception in Infants: Case Report and Literature Review.

Authors:  Carmine Noviello; Taisia Bollettini; Romano Mercedes; Alfonso Papparella; Stefano Nobile; Giovanni Cobellis
Journal:  Pediatr Infect Dis J       Date:  2021-11-01       Impact factor: 3.806

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