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Malaria masquerading as relapse of Hodgkin's lymphoma on contrast enhanced 18F-fluorodeoxyglucose positron emission tomography/computed tomography: A diagnostic dilemma
Address for correspondence: Dr. Sunil Jeph, Department of Nuclear Medicine and PET-CT, 10-B, K.G. Marg, New Delhi - 110 001, India. E-mail: suniljeph@gmail.com
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This article was originally published by Medknow Publications & Media Pvt Ltd and was migrated to Scientific Scholar after the change of Publisher.
Abstract
18Flurodeoxyglucose (18F-FDG) positron emission tomography/computed tomography (PET/CT) is nowadays routinely used in management of lymphoma patients. We here present a case of Hodgkin's lymphoma which showed 18F-FDG avid splenomegaly on PET/CT done for clinically suspected relapse. Further evaluation by peripheral smear examination revealed malaria. The patient was then started on anti-malarial medications and follow-up PET/CT revealed resolution of hypermetabolic splenomegaly. This report highlights that in endemic regions malaria can cause 18F-FDG avid splenomegaly and might mimic relapse of lymphoma.
Keywords
18F-Flurodeoxyglucose
lymphoma
malaria
positron emission tomography/computed tomography
spleen
INTRODUCTION
18Flurodeoxyglucose (18F-FDG) positron emission tomography/computed tomography (PET/CT) has become the imaging modality of choice for initial staging, follow-up and treatment response assessment in patients with Hodgkin's lymphoma and has proved superior to contrast enhanced CT (CECT) in these settings. 18F-FDG PET/CT has accuracy of almost 100% in diagnosing primary splenic involvement during initial staging of lymphoma. However, in the post-therapy setting its role for evaluation of secondary splenic involvement is limited. One of the pattern of splenic activity that help to detect splenic involvement on PET/CT is diffusely increased 18F-FDG uptake greater than that in the liver and bone marrow with or without corresponding CT lesions. In this context, we report a case of a patient with Hodgkin's lymphoma in remission presenting with 18F-FDG avid splenomegaly.
CASE REPORT
The present case report is about a 22-year-old male patient who presented with enlarged right cervical lymph node. Biopsy revealed-Hodgkin's lymphoma (mixed cellularity). 18F-FDG PET/CECT performed for staging revealed metabolically active lymph nodes on either side of the diaphragm [Figure 1a, broken arrows], enlarged spleen with multiple hypodense hypermetabolic, lesions [Figure 1a, arrow] (SUVmax= 9.4; Spleen SUVmax/liver SUVmax ratio = 3.76) and bone lesion. He was then given 6 cycles of chemotherapy and 18F-FDG PET/CECT was done for response evaluation. PET/CT showed complete metabolic response, with normal spleen uptake [Figure 1b, arrow] (Spleen SUVmax= 2.5, Liver SUVmax= 2.6 S/L ratio = 0.96). At 1-year later routine follow-up the patient complained of mild fever, lethargy and listlessness. In view of previous history of Hodgkin's lymphoma, relapse was suspected and 18F-FDG PET/CECT was advised. PET/CT revealed enlarged spleen with diffusely increased FDG uptake [Figure 2a–c, arrow] (SUVmax= 5.3; Liver SUVmax= 2.3 S/L ratio = 2.30). The first differential in the given clinical scenario was splenic relapse of lymphoma, however, a second differential diagnosis of some infective/inflammatory process was considered. On further evaluation, peripheral smear showed evidence of malaria parasite infection (Plasmodium vivax). The patient was then started on anti-malarials with complete clinical improvement. Follow-up PET/CT after 7 months revealed normalization of size and 18F-FDG uptake of spleen [Figure 2d, arrow] (SUVmax= 3.0; Liver SUVmax= 2.7 S/L ratio = 1.1). This clinical case can be easily misinterpreted as lymphoma relapse. Hence, malaria and other relevant (endemic) infective possibilities (Kala-Azar etc.) should be considered and further investigation, if warranted, should be advised.
DISCUSSION
PET/CT is a useful modality for staging and restaging of Hodgkin's lymphoma with high sensitivity and specificity.[1] Furthermore, it is a sensitive modality for early detection of relapse in asymptomatic patients making surveillance 18F-FDG PET/CT clinically important.[2] Splenic uptake on 18F-FDG PET can be due to a wide variety of causes such as lymphoma, anemia, granulocyte colony stimulating factor treatment, beta-thalassemia, inflammation and infections.[345678] Splenic uptake, greater than hepatic uptake, is a relatively reliable indicator of lymphomatous involvement of the spleen, in the absence of recent cytokine administration. In early stage HIV infection, diffusely increased splenic uptake is noted due to reactive stimulation of B-cells in the spleen. It can also be noted in sarcoidosis, malaria and many other inflammatory diseases. Post-therapeutic reactive splenic uptake is also noted after administration of granulocyte colony-stimulating factor for myelosuppression or high-dose interferon-alpha-2b adjuvant therapy for melanoma. Until date, only a single report by Liu et al. have demonstrated 18F-FDG uptake in spleen in case of malaria.[9]
Source of Support: Nil.
Conflict of Interest: None declared.
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