780

  • October 2019
  • PDF

This document was uploaded by user and they confirmed that they have the permission to share it. If you are author or own the copyright of this book, please report to us by using this DMCA report form. Report DMCA


Overview

Download & View 780 as PDF for free.

More details

  • Words: 1,421
  • Pages: 2
The British Journal of Radiology, 77 (2004), 780–781 DOI: 10.1259/bjr/25026914

E

2004 The British Institute of Radiology

Case report

Malignant mesothelioma of the tunica vaginalis testis 1

C W MAK, MD, 2T C CHENG, MD, 3S S CHUANG, MD, 1R H WU, MD, 1C K CHOU, MD and 1 J M CHANG, MD Department of 1Diagnostic Radiology, 2Urology and 3Pathology, Chi-Mei Foundation Medical Center, 901 Chung Hwa Road, Yung Kang, Tainan, Taiwan, Republic of China

Abstract. Malignant mesothelioma of the tunica vaginalis is rare, and is usually not diagnosed until surgery is undertaken. Reports on the ultrasound features of this tumour are limited. We present an unusual case with ultrasound features mimicking an adenomatoid tumour.

Malignant mesothelioma is an uncommon tumour arising in body cavities lined by mesothelium. The majority of these tumours are found in the pleura, peritoneum and less frequently pericardium. As the tunica vaginalis is a layer of reflected peritoneum, mesothelioma can occur in the scrotal sac. The nonspecific symptoms, broad age distribution and lack of tumour markers make pre-operative diagnosis of malignant mesothelioma of the tunica vaginalis difficult and indeed most of the reported cases were diagnosed at histology. Although ultrasound is considered the imaging modality of choice in evaluation of scrotal tumours, to date, reports on the ultrasound features of mesothelioma arising from tunica vaginalis are limited.

Case report A 41-year-old man visited the outpatient department with a 1-year history of a left scrotal mass. Initially, the scrotal mass had been ignored but as the scrotum became progressively enlarged, medical help was sought. Physical examination revealed a large tender mass occupying the left hemiscrotum. The right testis was normal. No lymph nodes were palpable in the inguinal regions. The transillumination test was positive. A ‘‘bulging’’ mass suspected to be due to inguinal hernia was also seen at right inguinal region. The past history was insignificant, the patient denied any trauma or infectious history to the scrotum. The patient also denied any exposure to asbestos in the past. Laboratory results including testicular tumour markers, alpha-feto-protein and beta human chorionic gonadotropin were normal. High resolution ultrasound using a 10 MHz linear transducer (GE LOGIQ 500; General Electric Medical Systems, Milwaukee, WI) showed a 2.1 cm61.3 cm hypoechoic mass with areas of colour Doppler flow demonstrated at left epididymal head (Figure 1). A moderate volume hydrocele was also found. Both testicles were normal in size and echopattern with no focal nodules detected. A minor varicocele was found in the left scrotum. With the clinical diagnosis of right inguinal hernia and left testicular tumour, right inguinal herniorrhaphy and left orchiectomy were performed. During the operation, a Received 6 October 2003 and accepted 17 December 2003.

780

Figure 1. Colour Doppler ultrasound demonstrates a welldefined hypoechoic nodule (arrow) occupying the left epididymal head, with a few areas of colour flow demonstrated. The left testis (T) was intact with no focal nodule detected. A hydrocele is also present.

hard papillary lesion was seen located close to the left epididymal head. Histology showed that the left epididymis was intact, the mass excised during the operation was a paratesticular tumour arising from the tunica vaginalis. Microscopically, the tumour was a well differentiated papillary mesothelioma consisting of complex papillary fronds lined by cuboid blandlooking nuclei with moderate amount of eosinophilic cytoplasm. Numerous foamy histiocytes were seen in the fibrovascular stroma (Figure 2). Immunohistochemistry of this tumour was positive for cytokeratin and vimentin, but negative for carcinoembryonic antigen, consistent with mesothelioma. Staging chest radiography and CT of the abdomen and pelvis revealed no evidence of metastasis; a 3 month follow-up physical examination and imaging studies were negative for recurrence.

Discussion Malignant mesothelioma of the tunica vaginalis is a rare primary tumour that occurs in a broad age range, with the highest incidence between 55 years and 75 years [1]. The British Journal of Radiology, September 2004

Case report: Mesothelioma of tunica vaginalis testis

Figure 2. Photomicrograph showing papillary fronds covered by bland-looking epithelial cells and aggregates of foamy histiocytes in the right hand side (haematoxylin and eosin stain, 2006).

Although trauma, herniorrhaphy and long term hydrocele [2] have been considered as the predisposing factors for development of malignant mesothelioma, the only well established risk factor is asbestos exposure [1, 3]. The ultrasound features of mesothelioma of the tunica vaginalis testis have not been widely reported. Hydrocele, either simple or complex is present and may be associated with: (1) well organized soft tissue fronds of mixed echogenicity (a hypoechoic centre surrounded by a hyperechoic rim) which extends into the hydrocele [4]; (2) multiple extratesticular nodular masses of increased echogenicity arising from the scrotal wall [5]; and (3) focal thickening of the tunica vaginalis testis with presence of nodularity [6]. The present case differs from the usual presentation; the mesothelioma demonstrated in our case consisted of a well-defined, slightly lobulated mass occupying the left epididymal head mimicking an epididymal tumour, and differentiation from the most common epididymal tumour, adenomatoid tumour was difficult. Adenomatoid tumour, also known as benign mesothelioma, occurs in a younger age group, usually in the 3rd to 4th decades. The ultrasound features of an adenomatoid tumour may be variable and usually consists of a welldefined round shaped nodule having variable echogenicity ranging from hypoechoic to hyperechoic. The adenomatoid tumour is mostly located in the epididymal tail. As this is a benign tumour, surgical excision is unnecessary unless it is large enough to cause discomfort to the patient. However for patients with mesothelioma, surgical intervention is necessary as this is an aggressive tumour. Patients with malignant mesothelioma of the tunica vaginalis frequently have a progressively enlarging hydrocele, and rapid re-accumulation of fluid after aspiration raises the suggestion of malignancy [7]. However fluid cytological analysis is frequently negative. Bruno et al [6] suggested direct ultrasound guided fine needle aspiration of the solid masses rather than fluid from the hydrocele,

The British Journal of Radiology, September 2004

however this is still subject to sampling error. Unlike the more common adenomatoid tumour, which is usually welldefined and round in shape, the present case demonstrated an oval and slightly lobulated mass. Surgery was therefore performed, due to the uncertainty of the diagnosis. Wolanske and Nino-Murcia [7] described the first colour Doppler ultrasound features of mesothelioma with decreased vascularity in the tumour compared with normal testicular parenchyma, consistent with the present case who also revealed relative hypovascularity of the tumour. Even though ultrasound may not be able to differentiate a malignant paratesticular tumour from the more common benign tumour the role of ultrasound cannot be ignored in clinical practice. Besides determining whether a lesion is cystic or solid it is also helpful in differentiating whether the lesion is a neoplasm or infectious process, hence avoiding unnecessary surgical intervention. The low cost of ultrasound, absence of ionizing radiation, convenience and ready availability, renders ultrasound the imaging modality of choice in the evaluation of intrascrotal, extratesticular mass compared with the other imaging modalities such as CT or MRI. In conclusion, malignant mesothelioma of the tunica vaginalis is a rare neoplasm, whenever a paratesticular mass is seen in the epididymis, the possibility of mesothelioma should be included in the differential diagnosis even when there is no history of asbestos exposure such as in the present case. As these tumours may mimic adenomatoid tumours, fine needle aspiration of the tumour may be contributory in making a pre-operative diagnosis in these patients. This is important as it affects the surgical approach and the patient’s prognosis. However, when a lobulated mass rather than a round shape is encountered, surgical intervention is recommended.

References 1. Plas E, Riedl CR, Pfluger H. Malignant mesothelioma of the tunica vaginalis: review of the literature and assessment of prognostic parameters. Cancer 1998;83:2437–46. 2. Gurdal M, Erol A. Malignant mesothelioma of tunica vaginalis testis associated with long term hydrocele: could hydrocele be an etiological factor? Int Urol Nephrol 2001;32:687–9. 3. Jones MA, Young RH, Scully RE. Malignant mesothelioma of the tunica vaginalis: a clinoco-pathologic analysis of 11 cases with review of the literature. Am J Surg Pathol 1995;19: 815–25. 4. Fields JM, Russell SA, Andrew SM. Ultrasound appearances of a malignant mesothelioma of the tunica vaginalis testis. Clin Radiol 1992;46:128–30. 5. Tyagi G, Munn CS, Kiser LC, Wetzner SM, Tarabulby E. Malignant mesothelioma of tunica vaginalis testis. Urology 1989;44:102–4. 6. Bruno C, Minniti S, Procacci C. Diagnosis of malignant mesothelioma of the tunica vaginalis testis by ultrasoundguided fine-needle aspiration. J Clin Ultrasound 2002;30:181–3. 7. Wolanske K, Nino-Murcia M. Malignant mesothelioma of the tunica vaginalis testis: atypical sonographic appearance. J Ultrasound Med 2001;20:69–72.

781

Related Documents

780
October 2019 7
780
May 2020 6
La Metro - 780
August 2019 6