Translate this page into:
Role for Positron Emission Tomography-Computed Tomography in Melioidosis
Address for correspondence: Prof. Irfan Ismail Ayub, Department of Pulmonary Medicine, Sri Ramachandra Medical College and Research Institute, SRIHER, Porur, Chennai, Tamil Nadu, India. E-mail: iia@rediffmail.com
-
Received: ,
Accepted: ,
This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
This article was originally published by Medknow Publications & Media Pvt Ltd and was migrated to Scientific Scholar after the change of Publisher.
Sir,
We read with interest the case series, “18-Fluorine-Fluorodeoxyglucose Positron Emission Tomography-Computed Tomography (PET-CT) in the Evaluation of the Great Masquerader Melioidosis: A Case Series,” by Kulkarni et al., published in the July–September issue of Indian Journal of Nuclear Medicine.[1] The authors have discussed the diagnostic utility of PET-CT in two patients with pyrexia of unknown origin (PUO), an indication for which PET-CT has been discussed in previously published literature.[234] The two patients were subsequently diagnosed with melioidosis. The authors have performed PET-CT before achieving a diagnosis of melioidosis, rather than part of evaluation of proven melioidosis, as the title suggests. However, we believe that the authors have raised an interesting point and led us to consider and propose PET-CT as an ideal investigation in the evaluation of proven melioidosis, with the illustration of a patient who recently presented to us.
A 34-year-old male with no significant history presented with 5 days of fever, cough, purulent sputum, and dyspnea. He had fever, tachycardia, tachypnea with room air peripheral saturation of 92%, and bilateral basilar crackles on chest auscultation. Abdominal and neurological examination was normal. Apart from anemia and leukocytosis, the blood hematology and biochemistry were normal. Serology for human immunodeficiency virus and scrub typhus were negative. Peripheral smear did not reveal malarial parasites. Chest radiograph [Figure 1a] showed bilateral lung nodules. He was diagnosed with community-acquired pneumonia, and after sending sputum and blood cultures, he was initiated on intravenous (IV) ceftriaxone and admitted in the ward. His sputum and blood culture [Figure 1b and c] confirmed Burkholderia pseudomallei, following which he was switched to IV ceftazidime. PET-CT was performed, which showed bilateral lung nodules with mild FDG uptake, some with feeding vessel sign, and mediastinal lymphadenopathy, with no evidence of uptake elsewhere [Figure 1d]. He improved clinically with 2 weeks of IV ceftazidime and was discharged on oral cotrimoxazole for 3 months. Chest radiograph 3 months later showed complete resolution [Figure 1e].

Although melioidosis commonly presents with pulmonary involvement, it can involve various other organs, including liver, spleen, lymph nodes, bones, joints, skin, and the central nervous system.[56] Treatment of meloidosis consists of a 2–4-week intensive phase to treat bacteremia, followed by an eradication phase to eliminate any residual focus of bacteria. The duration of this eradication phase is determined by extent of multifocal involvement and evidence of deep seated infection. The failure of eradication may lead to a future relapse.[7] Hence, it becomes important to image various organ systems, including abdomen and the axial and appendicular skeleton, to identify disease involvement elsewhere. Such a multimodality imaging approach, which may include an ultrasound of abdomen and magnetic resonance imaging of spine, may be cumbersome and can be replaced by a whole-body (PET-CT) scan, which can additionally detect disease in less common sites.
The use of PET-CT scan in the management of melioidosis is infrequently reported and was reviewed by the authors. Table 1 summarizes the available literature.[1891011] The indications for PET-CT in the reviewed publications were varied and included (1) to identify possible malignancy or metastases in a patient with clinical suspicion of malignancy,[81011](2) to look for other sites of organ involvement in a patient with blood culture-proven melioidosis,[9](3) in the evaluation of PUO and to identify an appropriate diagnostic investigation,[1] and (4) in the follow-up of patients with melioidosis and multiple site involvement to assess response to treatment.[810] Except for three, all the patients reported above had chronic symptoms and were being evaluated for possible malignancy or PUO. Two patients, who had symptoms for 4 days and 2 weeks, respectively, had thoracic radiology that was suspicious for malignancy and hence were subjected to PET-CT.[1011] Only in one patient, who had a subacute presentation, PET-CT was done after a positive culture of melioidosis, with the aim of searching for disease involvement in other sites, similar to our indication.[9] We believe that this indication has its benefits in avoiding multiple system-specific imaging, helps identify asymptomatic disease sites that may be responsible for future relapse if left untreated, and thus helps decide on duration of eradication therapy.[8]
| Number of patients, nature of publication, year of publication | Age; sex; primary symptoms (s); duration of symptoms, underlying comorbidity | Primary imaging; Indication for PET-CT scan; differential diagnosis | Pulmonary symptoms; lung involvement on PET-CT and SUV uptake; other organ involvement on PET | Diagnostic sample; treatment given; clinical outcome; duration of eradication phase |
|---|---|---|---|---|
| 1, case report, 2013[8] | 55 years; male; fever, weight loss, right shoulder pain; 6 months; none | X ray and subsequent MRI identified osteolytic lesion in the right humerus; to study extent of disease and identify other disease sites; malignant metastasis | None, incidental single left lower lobe of lung cavitating nodule with SUV 1.8; right humerus lesion | Bone marrow culture; appropriate antibiotic; improved with repeat PET-CT documenting response to treatment; 6 months |
| 1, case report, 2016[9] | 25 years; female; fever, weight loss, painful swelling of right wrist and knee; 3 weeks; none | MRI identified right palmar tenosynovitis, right femoral osteomyelitis and subsequent blood culture diagnostic; To identify other sites of disease involvement; none | None; multifocal involvement with unspecified uptake value; liver, lymph node, skin, muscle | Blood culture; appropriate antibiotic and surgical debridement; improved with repeat PET documenting response to treatment; 12 months |
| 1, case report, 2019[10] | 41; female; chest pain; 4 days; smoker | CXR revealed right midzone opacity; to rule out malignancy; malignancy | Chest pain and dyspnea; right lower lobe mass with mild-to-moderate uptake; none | Bronchial brushings and TBLC aided by EBUS guide sheath; appropriate antibiotic; improved; 3 months |
| 1, case report, 2020[11] | 57 years; male; fever, cough, chest pain; 2 weeks; systemic hypertension, hyperlipidemia | CXR: Left pleural effusion, lower zone subpleural opacity, hilar enlargement, CT thorax: Left lower lobe mass, pleural effusion, and mediastinal lymphadenopathy; to rule out malignancy; malignancy | Chest pain; left lower lobe lung mass with SUV 7.9, pleural effusion and hilar lymphadenopathy; none | Percutaneous biopsy; appropriate antibiotic; improved; 21 weeks |
| 2, case series, 2020[1] | 39 years male; fever, weakness, skin lesions; 3 months; diabetes mellitus | Ultrasound: Splenomegaly, ascites, bilateral pleural effusion, CXR: Right multiple pleural-based nodular lesions; evaluation of PUO; vasculitis, infection | None; lung nodules with unspecified SUV; lytic lesions of axial and appendicular skeleton, hepatosplenomegaly, lymphadenopathy | Blood culture; unspecified; unspecified; unspecified |
| 46 years male; fever; 4 months; diabetes mellitus | PET-CT scan; evaluation of PUO; infection | 2. None; none; multiple abscesses in the left kidney, abdominal lymphadenopathy | Image-guided biopsy and culture; unspecified; unspecified; unspecified |
PET-CT: Positron-emission tomography-computed tomography, SUV: Standardized uptake value, MRI: Magnetic resonance imaging, CXR: Chest X-ray, TBLC: Transbronchial lung cryobiopsy, EBUS: Endobronchial ultrasound, CT: Computed tomography, PUO: Pyrexia of unknown origin
Declaration of patient consent
The authors certify that they have obtained all appropriate patient consent forms. In the form, the patient has given his consent for his images and other clinical information to be reported in the journal. The patient understands that his name and initials will not be published and due efforts will be made to conceal identity, but anonymity cannot be guaranteed.
Financial support and sponsorship
Nil.
Conflicts of interest
There are no conflicts of interest.
Acknowledgment
We would like to thank Dr. Arunan Murali MD, Professor, Department of Radiology, for his contribution to reporting and interpretation of PET-CT scan.
References
- 18-fluorine-fluorodeoxyglucose positron emission tomography-computed tomography in the evaluation of the great masquerader melioidosis: A case series. Indian J Nucl Med. 2020;35:222-5.
- [Google Scholar]
- Contribution of 18F-FDG PET/CT in a case-mix of fever of unknown origin and inflammation of unknown origin: A meta-analysis. Acta Radiol. 2019;60:716-25.
- [Google Scholar]
- FDG-PET/CT in fever of unknown origin working group. Diagnostic yield of FDG-PET/CT in fever of unknown origin: A systematic review, meta-analysis, and Delphi exercise. In: Clin Radiol. Vol 72. 2017. p. :764-71.
- [Google Scholar]
- Diagnostic utility of fluorodeoxyglucose positron emission tomography/computed tomography in pyrexia of unknown origin. Indian J Nucl Med. 2015;30:204-12.
- [Google Scholar]
- Melioidosis: Spectrum of radiological manifestations. Saudi J Med Med Sci. 2016;4:74-8.
- [Google Scholar]
- 2020 Review and revision of the 2015 Darwin melioidosis treatment guideline; paradigm drift not shift. PLoS Negl Trop Dis. 2020;14:e0008659.
- [Google Scholar]
- Melioidosis in a European traveler without comorbidities: A case report and literature review. Int J Infect Dis. 2013;17:e781-3.
- [Google Scholar]
- Multifocal melioidosis with femoral osteomyelitis in a healthy 25-year-old traveller. BMJ Case Rep. 2016;2016:bcr2016216356.
- [Google Scholar]
- Chronic pulmonary melioidosis masquerading as lung malignancy diagnosed by EBUS guided sheath technique. Respir Med Case Rep. 2019;28:100894.
- [Google Scholar]
- A mimic of bronchogenic carcinoma-Pulmonary melioidosis. Respir Med Case Rep. 2020;29:101006.
- [Google Scholar]