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. 2022 Apr;303(1):173-181.
doi: 10.1148/radiol.211737. Epub 2021 Dec 7.

Abdominal US in Pediatric Inflammatory Multisystem Syndrome Associated with SARS-CoV-2 (PIMS-TS)

Affiliations

Abdominal US in Pediatric Inflammatory Multisystem Syndrome Associated with SARS-CoV-2 (PIMS-TS)

Riwa Meshaka et al. Radiology. 2022 Apr.

Abstract

Background Children with pediatric inflammatory syndrome temporally associated with SARS-CoV-2 (PIMS-TS), also known as multisystem inflammatory syndrome in children, present with abdominal pain among other nonspecific symptoms. Although initial imaging features of PIMS-TS have been reported, the duration of sonographic features remains unknown. Purpose To describe the abdominal US features of PIMS-TS at initial presentation and follow-up. Materials and Methods A retrospective review of children and young adults presenting with clinical features suspicious for PIMS-TS between April 2020 and June 2021 was carried out. US features were documented and reviewed at initial presentation and follow-up. Descriptive statistics were used and interobserver variability was calculated. Results Of 140 children and young adults presenting with suspected PIMS-TS, 120 had confirmed PIMS-TS (median age, 9 years; interquartile range, 7-12 years; 65 male patients) and 102 underwent abdominal US at presentation. PIMS-TS was present as a single abnormality in 109 of the 120 patients (91%) and abdominal symptoms were present in 104 of the 109 (95%). US examinations were abnormal in 86 of 102 patients (84%), with ascites being the most common abnormality in 65 (64%; 95% CI: 54, 73). Bowel wall thickening was present at US in 14 of the 102 patients (14%; 95% CI: 7, 20) and mesenteric inflammation was present in 16 (16%; 95% CI: 9, 23); all of these patients presented with abdominal symptoms. Among the patients with bowel wall thickening, the distal and terminal ileum were most involved (eight of 14 patients, 57%). Abdominal symptoms decreased to seven of 56 patients (13%) in those followed up at 6 months. Thirty-eight patients underwent follow-up US, and the presence of bowel inflammation had decreased to three of 27 patients (11%; 95% CI: -1, 23) in those followed up for less than 2 months and 0 of 17 (0%) in those followed up for more than 2 months. Conclusion Of 102 patients with pediatric inflammatory multisystem syndrome temporally associated with SARS-CoV-2 who underwent US at presentation, 14 (14%) had abdominal US findings of bowel inflammation and 16 (16%) had mesenteric edema. All US abnormalities resolved after 2 months. © RSNA, 2022 Online supplemental material is available for this article. See also the editorial by van Rijn and Pajkrt in this issue.

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Conflict of interest statement

Disclosures of conflicts of interest: R.M. No relevant relationships. F.C.W. No relevant relationships. M.G. Participation on a data safety monitoring board or advisory board at St Georges Hospital. S.E. No relevant relationships. S.C.S. No relevant relationships. O.J.A. No relevant relationships. K.M. No relevant relationships. M.P.H. No relevant relationships. P.D.H. No relevant relationships. A.D.C. No relevant relationships. M.J.E. No relevant relationships. E.P.G. Secretary of the Quality Standards Working Group at British Society for Paediatric Gastroenterology. T.W. Contract to provide paid central read reports for Alimentive.

Figures

None
Graphical abstract
Flowchart shows study case definition with symptoms, biochemical
markers, and US findings at presentation and early (<2 months) and
late (>2 months) follow-up. CRP = C-reactive protein, EPR =
electronic patient record, FCP = fecal calprotectin, F/Up = follow-up,
PIMS-TS = pediatric inflammatory multisystem syndrome temporally associated
with SARS-CoV-2, Sympt = symptoms.
Figure 1:
Flowchart shows study case definition with symptoms, biochemical markers, and US findings at presentation and early (<2 months) and late (>2 months) follow-up. CRP = C-reactive protein, EPR = electronic patient record, FCP = fecal calprotectin, F/Up = follow-up, PIMS-TS = pediatric inflammatory multisystem syndrome temporally associated with SARS-CoV-2, Sympt = symptoms.
Graph compares monthly number of patients with suspected pediatric
inflammatory multisystem syndrome temporally associated with SARS-CoV-2
(PIMS-TS) referred to our tertiary hospital with the reported cases of
COVID-19 in the United Kingdom. COVID-19 case data are from a publicly
available database at https://coronavirus.data.gov.uk.
Figure 2:
Graph compares monthly number of patients with suspected pediatric inflammatory multisystem syndrome temporally associated with SARS-CoV-2 (PIMS-TS) referred to our tertiary hospital with the reported cases of COVID-19 in the United Kingdom. COVID-19 case data are from a publicly available database at https://coronavirus.data.gov.uk.
Noncontrast US scan (transverse plane) of the right iliac fossa in a
7-month-old boy with pediatric inflammatory multisystem syndrome temporally
associated with SARS-CoV-2. Image shows extensive inflammatory change with
abnormal lymph nodes in the right iliac fossa (arrow).
Figure 3:
Noncontrast US scan (transverse plane) of the right iliac fossa in a 7-month-old boy with pediatric inflammatory multisystem syndrome temporally associated with SARS-CoV-2. Image shows extensive inflammatory change with abnormal lymph nodes in the right iliac fossa (arrow).
Noncontrast US scan (transverse plane) of the right iliac fossa in a
10-year-old boy with pediatric inflammatory multisystem syndrome temporally
associated with SARS-CoV-2. Image shows distal ileal thickening (measured
between “+” markers and labeled “1”) and ascites
(arrow).
Figure 4:
Noncontrast US scan (transverse plane) of the right iliac fossa in a 10-year-old boy with pediatric inflammatory multisystem syndrome temporally associated with SARS-CoV-2. Image shows distal ileal thickening (measured between “+” markers and labeled “1”) and ascites (arrow).
Noncontrast US scan (longitudinal plane) in an 18-year-old man with
pediatric inflammatory multisystem syndrome temporally associated with
SARS-CoV-2. Image shows an extensive thrombus in the inferior vena cava
(arrow).
Figure 5:
Noncontrast US scan (longitudinal plane) in an 18-year-old man with pediatric inflammatory multisystem syndrome temporally associated with SARS-CoV-2. Image shows an extensive thrombus in the inferior vena cava (arrow).
Diagram shows sites of bowel inflammation detected on presentation US
scans in 14 patients with pediatric inflammatory multisystem syndrome
temporally associated with SARS-CoV-2. Nine patients had single-site
involvement and five patients had more than one site involved. Numbers are
instances of bowel inflammation at various sites in the 14
patients.
Figure 6:
Diagram shows sites of bowel inflammation detected on presentation US scans in 14 patients with pediatric inflammatory multisystem syndrome temporally associated with SARS-CoV-2. Nine patients had single-site involvement and five patients had more than one site involved. Numbers are instances of bowel inflammation at various sites in the 14 patients.

Comment in

References

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Supplementary concepts