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Review
. 2020 Feb 27;20(1):162.
doi: 10.1186/s12885-020-6648-3.

Malignant mesothelioma of the tunica vaginalis testis: a rare case and review of literature

Affiliations
Review

Malignant mesothelioma of the tunica vaginalis testis: a rare case and review of literature

Mingaile Drevinskaite et al. BMC Cancer. .

Abstract

Background: Malignant mesothelioma of the tunica vaginalis is a rare tumour which comprises less than 1% of all mesotheliomas.

Case presentation: 69-years old patient with painful hard mass and hydrocele in the right scrotum to whom a right hydrocelectomy was performed. Any history of scrotal trauma or exposure to asbestos was not present. Excisional biopsy revealed a multinodular tumour with focal areas of necrosis and infiltrative growth. According to morphological and immunohistochemical findings, diagnosis of malignant biphasic mesothelioma of the tunica vaginalis testis was made. Two months after hydrocelectomy, right inguinal orchidectomy was performed. Post-surgical whole body CT scan revealed paraaortic and pararenal lymphadenopathy, likely to be metastatic. Adjuvant treatment with 6 cycles of cisplatin and pemetrexed was applied. After 3 cycles of chemotherapy, CT scan showed progression and the treatment was changed to gemcitabine 1 month after.

Conclusions: Although malignant mesothelioma of the tunica vaginalis is a rare malignancy, it poses a diagnostic challenge which can mimic common inguinal or scrotal diseases such as hydrocele. Despite aggressive surgical procedures or adjuvant therapies, the prognosis remains poor.

Keywords: Malignant mesothelioma; Tunica vaginalis.

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Conflict of interest statement

The authors declare that they have no competing interests.

Figures

Fig. 1
Fig. 1
Histologic patterns, HE. (a) Nests of immature epithelioid cells, × 20; (b) Sarcomatoid areas mimicking desmoplastic response of the widely dispersed epithelial cells, × 10; (c) A highly cellular tumour with glomerular-like epithelial tufts projecting into cystic epithelium lined spaces, × 20; (d) An insidious right-to-left transition from epithelial to sarcomatous components, × 20; (e) Intracystic tumour with paratesticular spread, × 2; (f) The more-typical tubulopapillary pattern of mesothelioma, × 20
Fig. 2
Fig. 2
Resected specimen shows 3 cm × 7 cm nodular masses encasing the compressed testicular tissue
Fig. 3
Fig. 3
Enlarged to 21 × 15 mm infrarenal paraaortic masses in computed tomography axial view
Fig. 4
Fig. 4
Infrarenal paraaortic masses enlarged to 21 × 25 mm, next to aortic bifurcation masses enlarged to 15 mm in computed tomography coronal view
Fig. 5
Fig. 5
Radiological progression of disease with paraaortic mass, enlarged to 32 × 28 mm in computed tomography axial view
Fig. 6
Fig. 6
Paraaortic mass enlarged to 32 × 28 mm and mass next to aortic bifurcation, enlarged to 31 mm

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