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Interesting Image
41 (
3
); 396-397
doi:
10.25259/IJNM_14_25

Peritoneal Dialysis-associated Peritonitis: Early Detection with 18F-Fluorodeoxyglucose PET/CT

Department of Nuclear Medicine, Central University Hospital of Asturias, Oviedo, Spain

*Corresponding author: Dr. Juan Pablo Suárez Fernández, Department of Nuclear Medicine, Central University Hospital of Asturias, Oviedo, Spain. juanpablosuarez@yahoo.es

Licence
This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-Share Alike 4.0 License, which allows others to remix, transform, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.

How to cite this article: Suarez JP, Rodriguez L, Dominguez ML, Vigil C, Martin N, Gonzalez FM. Peritoneal Dialysis-associated Peritonitis: Early Detection with 18F-Fluorodeoxyglucose PET/CT. Indian J Nucl Med. 2026;41:396-7. doi: 10.25259/IJNM_14_25.

Abstract

Peritonitis is a common and serious complication of peritoneal dialysis (PD). We present the case of a 39-year-old man in a PD program who suffered a septic shock of unknown origin. 18F-Fluorodeoxyglucose positron emission tomography/computed tomography (PET/CT) was performed to find the source of infection after clinical improvement and prolonged antibiotic therapy. PET/CT revealed several abdominopelvic hypermetabolic foci consistent with PD-associated peritonitis, but it was not confirmed neither by clinical evaluation nor peritoneal fluid culture. Twelve days later, the patient developed clinical symptoms compatible with peritonitis, and subsequent dialysis effluent culture was positive for Streptococcus vestibularis.

Keywords

18F fluorodeoxyglucose positron emission tomography/computed tomography
Peritoneal dialysis
Peritonitis

The diagnosis of peritoneal dialysis (PD)-associated peritonitis requires any two of the following features: (a) Clinical features consistent with peritonitis, i.e., abdominal pain or cloudy dialysis effluent; (b) dialysis effluent white cell count >100/μl (after a dwell time of at least 2 h), with >50% neutrophils; and (c) positive dialysis effluent culture.[1] Whenever peritonitis is suspected, PD effluent should be tested for differential cell count, Gram stain, and bacterial culture.[1] Conventional imaging (ultrasound, computed tomography [CT]) has a limited role in the diagnosis of PD-associated peritonitis because their findings are often nonspecific[2] tuberculous peritonitis is common in these patients due to immunosuppression, and it can be detected efficiently with 18F fluorodeoxyglucose (FDG) positron emission tomography (PET)/CT [Fig 1], though peritoneal carcinomatosis is a known cause of false-positive results.[3] Prompt clinical diagnosis and early initiation of antibiotic therapy are key to successful treatment, but at the firststages of infection and/or after prolonged antibiotic therapy, typical clinical symptoms can be absent, and PD effluent culture can be sterile,[1] as it happened in our case. To the best of our knowledge, this is the first report of the detection of nontuberculous PD-associated peritonitis with 18F FDG PET/CT imaging.

Maximum intensity projection (MIP) positron emission tomography (PET) image (a) Demonstrates the presence of several hypermetabolic foci located within the abdominopelvic cavity. It must be noted that whole body MIP image does not show usual fluorodeoxyglucose biodistribution, as there is no renal or urinary bladder uptake, most likely due to nonfunctional kidneys. (b) Transaxial PET, (c) Computed Tomography (CT) and (d) fused PET/CT images reveal free abdominopelvic fluid, with high metabolic activity in right iliac fossa (arrows in c and d). Several hypermetabolic lesions are found as well in the peritoneal membrane next to some intestinal loops, with highest metabolic activity located in the left iliac fossa (maximum standarised uptake value - 16.64), (e) as shown in transaxial PET, (f) CT and (g) fused PET/CT images (arrowheads in e and g). Based on these findings and given the patient’s clinical signs, bacterial peritonitis secondary to peritoneal dialysis was suspected, and ultimately confirmed by peritoneal fluid culture
Fig 1: Maximum intensity projection (MIP) positron emission tomography (PET) image (a) Demonstrates the presence of several hypermetabolic foci located within the abdominopelvic cavity. It must be noted that whole body MIP image does not show usual fluorodeoxyglucose biodistribution, as there is no renal or urinary bladder uptake, most likely due to nonfunctional kidneys. (b) Transaxial PET, (c) Computed Tomography (CT) and (d) fused PET/CT images reveal free abdominopelvic fluid, with high metabolic activity in right iliac fossa (arrows in c and d). Several hypermetabolic lesions are found as well in the peritoneal membrane next to some intestinal loops, with highest metabolic activity located in the left iliac fossa (maximum standarised uptake value - 16.64), (e) as shown in transaxial PET, (f) CT and (g) fused PET/CT images (arrowheads in e and g). Based on these findings and given the patient’s clinical signs, bacterial peritonitis secondary to peritoneal dialysis was suspected, and ultimately confirmed by peritoneal fluid culture

Author contribution:

JS: Wrote the manuscript and created the figure; LR, MLD, CV, NM and FG: Discussed the results and contributed to the drafting of the final manuscript

Ethical approval:

Institutional Review Board approval is not required.

Declaration of patient consent:

The authors certify that they have obtained all appropriate patient consent forms. In the form, the patient has given consent for their images and other clinical information to be reported in the journal. The patient understand that the patient’s names and initials will not be published and due efforts will be made to conceal their identity, but anonymity cannot be guaranteed.

Conflicts of interest:

There are no conflicts of interest.

Use of artificial intelligence (AI)-assisted technology for manuscript preparation:

The authors confirm that there was no use of artificial intelligence (AI)-assisted technology for assisting in the writing or editing of the manuscript and no images were manipulated using AI.

Financial support and sponsorship: Nil.

References

  1. , . Peritoneal dialysis-associated peritonitis. Clin J Am Soc Nephrol. 2019;14:1100-5.
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  2. , , . Continuous ambulatory peritoneal dialysis-a guide to imaging appearances and complications. Insights Imaging. 2013;4:85-92.
    [CrossRef] [PubMed] [Google Scholar]
  3. , , , . Intense FDG activity in peritoneal tuberculosis mimics peritoneal carcinomatosis. Clin Nucl Med. 2007;32:244-6.
    [CrossRef] [PubMed] [Google Scholar]

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