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Non-Hodgkin's lymphoma presenting as a primary bladder tumor: a case report

  • José A Díaz-Peromingo1Email author,
  • Javier Tato-Rodríguez2,
  • Paula M Pesqueira-Fontán1,
  • Sonia Molinos-Castro1,
  • María C Gayol-Fernández1 and
  • Juliusz P Struzik2
Journal of Medical Case Reports20104:114

https://doi.org/10.1186/1752-1947-4-114

Received: 28 October 2008

Accepted: 26 April 2010

Published: 26 April 2010

Abstract

Introduction

Primary lymphoma of the bladder represents 0.2% of all bladder malignancies. Secondary involvement of the bladder by malignant lymphoma occurs in 10% to 50% of cases. Most lymphomas of the bladder are non-Hodgkin's lymphomas of the B-cell type, with preponderance among women. The impact of positron emission tomography (PET) on tumor staging has recently become very important due to its use in the study of diagnosis extension and individual therapy design.

Case presentation

We report the case of a 79-year-old Caucasian man with intermittent haematuria as the presenting symptom of non-Hodgkin's lymphoma of the bladder. He was first diagnosed with primary lymphoma of the bladder using the current staging method, but a positron emission tomography study subsequently revealed that he instead had a secondary involvement of the bladder.

Conclusion

The staging of non-Hodgkin's lymphomas, which is useful in order to plan accurate therapy, has been changing since the introduction of positron emission tomography scanning. Primary lymphomas of the bladder, although very rare, may be even more uncommon when this imaging technique is used to assess the extension of the disease. Although the interpretation of this technique has some limitations that should be taken into account, the extensive use of positron emission tomography should nonetheless help improve the diagnosis of this disease.

Introduction

Most tumors of the bladder are derived from the epithelium. Non-epithelial tumors are extremely rare. Among these, leiomyosarcomas are the most common in adults and rhabdomyosarcomas are the most common in children [1]. Metastatic tumors more frequently affect the bladder neck and the deep trigone and represent approximately 15% of all known bladder malignancies [2].

Meanwhile, primary lymphomas of the bladder are very rare and were first described by Eve in 1885 [3]. They represent 0.2% of all known bladder cancers [4]. Secondary bladder involvement is reported in 10% to 50% of cases, with a maximum incidence between the fourth and sixth decades of life [5, 6]. Most lymphomas of the bladder are low-grade non-Hodgkin's lymphomas (NHL) of the B-cell type [1, 7]. Women are affected more frequently than men [4, 8].

The most frequent symptoms of bladder lymphomas are gross haematuria followed by concomitant urinary tract infection, dysuria and increased urinary frequency [9]. Other complications like hydronephrosis, fistulas or involvement of the entire bladder are very rare [10].

Usually, the diagnosis of primary lymphoma of the bladder is one of exclusion. It is made in the absence of any other nodal or extranodal involvement after biopsy with immunohistochemical study, and after a negative study of disease extension, which includes bone marrow biopsy and computed tomography (CT) [11]. This approach is changing with the introduction of positron emission tomography (PET) to assess for other nodal or extranodal involvement when a possible primary lymphoma of the bladder is suspected. In this case report, we present a case of primary lymphoma of the bladder in which PET scanning changed the diagnosis to extended NHL. We review the literature focusing on the use of PET in the assessment of tumor extension.

Case presentation

A 79-year-old Caucasian, Spanish man was admitted to our hospital because of intermittent painful gross haematuria lasting for seven days. He smoked 20 cigarettes per day and reported having an appendectomy 40 years prior to presentation. He had worked as a seaman in his youth and was currently retired. He took no medications.

Results of his general examination were normal. His rectal examination revealed an enlarged prostate, grade I/IV, with no masses or nodules. Results of his analytical studies including serum chemistry, prostate specific antigen (PSA), and coagulation studies were normal. A mild anaemia (hemoglobin = 11.3 g/L) with a normal mean corpuscular volume was reported. His erythrocyte sedimentation rate (ESR) was 67 mm per hour. An ultrasonographic study of his abdomen had normal results, except for an irregular border of the right lateral wall of his bladder.

Meanwhile, his intermittent gross haematuria continued, sometimes with associated blood clots. A cystoscopy procedure was performed and an irregular mass affecting his right antero-lateral wall was found. Biopsy revealed a diffuse, large B-cell lymphoma with the following immunohistochemical findings: CD20-, BCL6-, and DC10-positive. Meanwhile, his MIB1 had a high proliferation level. CT scans of his chest, abdomen and pelvis were performed and showed neither enlarged nodes nor liver or spleen involvement. No metastatic lesions were likewise found. His peripheral blood smear test was normal, as were his direct and indirect Coombs tests, serum protein counts, and plasma serum immunoglobulins. His β2-microglobulin was 2.79 mg/dL (normal range = <0.27 mg/dL).

Results of a whole body PET study of our patient (Figures 1 and 2) revealed two nodes with increased metabolism in the left part of his neck, and another area close to his left supraclavicular space, which was suggestive of nodal involvement. An enlarged left mediastinal lymph node was also found on our patient. His left suprarenal gland showed hypermetabolism. His abdomen appeared to have multiple lymph node infiltrates affecting his lumbar region in particular, both his iliac lymphatic chains, and those close to his bladder with associated hypermetabolism of his bladder walls. Results of his bone marrow biopsy were also normal.
Figure 1

Coronal view shows multiple areas of increased metabolism affecting the neck, mediastinum, left suprarenal gland, abdominal lymph nodes and the bladder.

Figure 2

This image shows the PET findings in a three-dimensional projection view.

Our patient was started on a treatment with CNOP (cyclophosphamide, mitoxantrone, vincristine and prednisolone) and monoclonal antibodies anti-CD20. He showed good tolerance and initial response to this treatment.

Conclusion

Our patient showed no abnormalities on the CT study. Nevertheless, significant nodal and extranodal (suprarenal gland) extension of his disease was discovered upon performing a PET study.

PET with 2- [fluorine 18] fluoro-2-deoxy-D-glucose (FDG) is increasingly being used in combination with CT to evaluate thoracic and abdominopelvic malignancies [12]. A common systemic malignancy involving the pelvis is NHL. Whole-body PET is useful in the detection of a wide variety of both primary and metastatic malignancies because of the high glycolytic rate that the malignant tissue presents. The presence of FDG uptake in benign inflammatory conditions may limit the specificity of PET. Sensitivity for the detection of malignant lesions is about 97% and the positive predictive value is 94%. This technique is promising both in determining the nature of a localized lesion, as well as in defining the systemic extent of a malignant disease [13].

A number of studies have shown FDG-PET to be useful and in fact superior to CT for primary staging and assessment of disease extension in both Hodgkin's disease and NHL. The technique is reported to have sensitivities of 82% to 99% and specificities of 99% to 100% [14]. Although data regarding the use of in-line FDG-PET-CT systems in evaluating lymphoma are inconclusive, preliminary results appear to indicate that this technique is useful when a guided biopsy procedure is needed [15]. In one study that compared the diagnostic performance of PET alone, CT alone, and fused images for restaging or follow-up of patients with malignant lymphoma, 50 patients with NHL were included. In this study, the interpretation of PET alone (sensitivity = 86.1%, specificity = 99.4%, accuracy = 91.0%), and fused images (98.0%, 99.4%, and 99.2%, respectively) yielded significantly better diagnostic performance than CT alone (59.4%, 96.1%, 91.0%; P < 0.001). In particular, findings in cervical, supraclavicular and extranodal regions were more accurately identified using PET (P < 0.05) [16]. With regard to staging, FDG-PET is more sensitive and specific than conventional staging methods in FDG avid lymphomas such as Hodgkin's lymphoma and most aggressive NHLs.

In assessing a patient's response to therapy, FDG-PET at the end of treatment seems to aid considerably in differentiating between residual masses with and without residual lymphoma. Concerning treatment planning, meanwhile, in the context of a combined-modality therapy, radiotherapy for lymphomas is moving towards more conformal techniques to reduce the irradiated volume and to include only the macroscopic lymphoma. In this context, accurate imaging is essential, and FDG-PET in combination with CT scan is increasingly being used. The availability of PET and CT scanners suited for virtual simulation has aided in this process [17].

The limitations of FDG-PET in detecting lymphomas have included variable FDG uptake in low-grade lymphomas; physiologic activity in muscles, bone marrow, bowels, and the urinary system; and FDG uptake in inflammatory or infectious processes, any of which may mask or mimic tumor signals [18]. Another limitation in the analysis of the pelvis and the urinary tract is the physiological excretion of radiotracers [19].

This case suggests the need for extensive lymphoma staging, and especially the need for PET implementation, in order to make an accurate diagnosis of the extension of the disease and to properly design a course of treatment.

Consent

Written informed consent was obtained from our patient for publication of this case report and any accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of this journal.

Declarations

Authors’ Affiliations

(1)
Department of Internal Medicine, Hospital da Barbanza
(2)
Department of Urology, Hospital da Barbanza

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Copyright

© Díaz-Peromingo et al; licensee BioMed Central Ltd. 2010

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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