An unusual case of asymptomatic non-urothelial bladder tumour

Highlights

• •Bladder paragangliomas are rare and account for less than 0.05% of all bladder tumours.
• •They can present as incidental findings without any clinical symptoms.
• •Due to the non-specific nature, they are often not part of the urologists differential diagnoses.
• •Pre-operative suspicion and management are essential to reduce anaesthetic risk.

Abstract

Introduction

Non-urothelial tumours are rare and account for less than 5% of all bladder tumours. Bladder paragangliomas also known as extra-adrenal pheochromocytomas are of the non-urothelial subgroup. We present an unusual case of asymptomatic bladder paraganglioma.

Case report

A 77 year old lady presented with acute abdominal pain was found to have an incidental enhancing nodule in the bladder. During cystoscopy and transurethral resection the patient experienced significant fluctuations in blood pressure that required anaesthetic adjustments. Review of histology confirmed a diagnosis of bladder paraganglioma.

Discussion

Most bladder paraganglioma cases present with sympathomimetic related symptoms and microscopic haematuria but our patient was asymptomatic which resulted in inadequate pre-operative optimisation and high anaesthetic risk. Majority of paragangliomas are benign but there is a 20-40% chance of malignancy. The management options will predominantly depend on whether disease is localised, regional, metastatic or recurrent in nature.

Conclusion

Due to the non-specific nature of disease, variability of presentations and rare incidence, bladder paragangliomas are often not part of the urologists’ differential diagnoses. In our opinion, establishing guidelines should assist to achieve a balance between anaesthetic risks, cystoscopy and follow up.

1. Introduction

Bladder tumours can be subdivided into urothelial and non-urothelial tumours. They usually present as urothelial tumours, with non-urothelial tumours accounting for less than 5% of all bladder tumours. Bladder paragangliomas (also known as extra-adrenal pheochromocytomas) are of the non-urothelial subgroup [1]. We present an unusual case of asymptomatic bladder paraganglioma.

2. Case report

A 77 year old lady presented to the emergency department with acute abdominal pain. A Computed Tomography (CT) abdomen and pelvis with contrast performed demonstrated an incidental enhancing nodule anteriorly in the bladder measuring 2.2 cm (Fig. 1, Fig. 2). The patient was referred to the urology multi-disciplinary team (MDT) which decided further investigation was warranted with cystoscopy and a transurethral resection.

Fig. 1.

Coronal view showing bladder enhancing nodule.

Fig. 2.

Axial section demonstrating bladder enhancing nodule.

During the resection under general anaesthesia, the patient experienced significant fluctuations in blood pressure (BP) that required intermittent breaks and pharmacological adjustment. Macroscopically the tumour was a tan brown lesion with normal smooth bladder mucosa.

Review of histology confirmed a diagnosis of a bladder paraganglioma (Figs. 3, 4 and 5). CD56 and chromogranin immunostains are commonly used neuroendocrine markers. The brown staining on both immunostains shows evidence for neuroendocrine cells. As the patient had multiple intra-abdominal surgeries and there was no evidence of metastatic spread on the CT scan, the MDT’s decision was for 3 monthly follow-up with surveillance cystoscopies post-resection and depending on clinical features for further biochemical and radiological investigations as needed.

Fig. 3.

Low power view with Hematoxylin & Eosin stain demonstrating the solid tumour compressing muscle.

3. Discussion

The incidence of bladder paragangliomas is less than 0.05% of all bladder tumours [2] and less than 1% of all paragangliomas [3]. The mean patient age was 43.3 years (range 11-84) and has an almost equal male to female ratio of 1.07:1 [4].

A systemic review found 106 patients and demonstrated that majority of cases presented with catecholamine secretion leading to sympathomimetic related symptoms. The most common symptoms at presentation in decreasing order are hypertension, headaches, haematuria and syncope/palpitations [3]. They are often triggered during micturition hence termed ‘micturition attacks’ and are reported in 52.8% of patients [3]. Patients were reported to have haematuria in 47-60% of cases and most were of microscopic nature [3]^, [5]. The literature dictates that only 27% of patients had no indication of hormonal activity [6], and 3% of cases were incidental findings [3]. Our patient had moderate hypertension controlled with one anti-hypertensive, did not experience any other symptoms and had a negative urine specimen.

In an asymptomatic incidental bladder lesion it is almost impossible to diagnose bladder paraganglioma without histological diagnosis. Suspicious cases are usually investigated by measuring the level of catecholamine and its metabolites (metanephrine and vanillylmandelic acid secretion) in blood and urine [7]^, [8]. A flexible cystoscopy may be warranted as a form of preliminary investigation especially in symptomatic patients. CT or Magnetic Resonance Imaging can identify the location and extent of the invasion. Advanced methods with the use of nuclear medicine scanning using radioisotope ¹²³- or ¹³¹-iodine-metaiodinebenzylguinidine and Positron Emission Tomography should be considered, and is the imaging modality of choice for localizing small tumours [9]^, [10]^, [11].

Prior to any surgical intervention, careful pre-operative management is required. A pre-operative treatment period of 1-3 weeks with alpha-adrenergic blockade is recommended to avoid intra/post-operative complications such as hypertensive crisis, arrhythmias, myocardial infarction and pulmonary oedema. Beta-adrenergic blockade can be considered pre-operatively, especially in patients with persistent arrhythmias or tachycardia, but must never be initiated before alpha-adrenergic blockade because doing so leads to unopposed alpha-adrenergic vasoconstriction which can lead to a life-threatening crisis [12]. Good symptomatic control and a target low BP for age are features of adequate medical optimisation.

The macroscopic appearance of tan brown lesion seen on cystoscopy is not pathognomic for any form of bladder tumour. According to literature, majority of paragangliomas are benign with a 20-40% of chance of malignancy [13]. There is no single parameter that can predict the malignant potential of paragangliomas. In practice, the only reliable criterion for malignancy is the presence of distant metastases [12]. At present, novel molecular biomarkers are being investigated for their utility in defining malignant tumours.

The management options will predominantly depend on whether disease is localised, regional, metastatic or recurrent in nature. Patients with disease dissemination will require management with a combination of surgery, chemotherapy and/or radiotherapy [14]^, [15]. There is currently no consensus on the management of localised/regional cases. Some studies advocate a partial or complete cystectomy as there is a chance of recurrence from chromaffin cells in the sympathetic plexus of detrusor muscle, and a transurethral resection approach does not adequately excise the lesion. Most however agree that regular follow-up is necessary [13]. Prognostic factors that can be used as a guide include large size (>5 cm diameter), local tumour extension, and the presence of necrotic areas [12]^, [13].

4. Conclusion

Due to the non-specific nature of disease, variability of presentations and rare incidence, bladder paragangliomas are often not part of the urologist’s differential diagnoses. This article hopes to add to the limited cases of asymptomatic incidental bladder paragangliomas in the literature and illustrate the importance of suspecting its possibility to reduce operative risk. The involvement of the MDT is essential to ensure patient safety. We support the notion that all cases necessitate long-term follow up which will be dictated by the extent of disease involvement. In our opinion, establishing guidelines should assist to achieve a balance between anaesthetic risks, cystoscopy and follow up. Further research is required to establish best practice in localised bladder paraganglioma management.

Conflicts of interest

All authors declare that there is no conflict of interest.

Funding

This research received no specific grant from any funding agency in the public, commercial, or not - for - profit sectors.

Ethical Approval

Not applicable.

Consent

Written informed consent was obtained from the patient for their anonymised information to be published in this article.

Author contribution

DC and EA researched literature and conceived the study. DC wrote the first draft of the manuscript.

All authors reviewed and edited the manuscript and approved the final version of the manuscript.

Guarantor

SS is the guarantor of the study.

Fig. 4.

CD56 stain with brown colour highlighting positive paraganglioma tumour cells. No necrotic areas or mitoses were seen. Antigen Ki-67 is less than 5%.

Fig. 5.

Chromogranin immunostain with brown colour demonstrating positive neuroendocrine cells.