Squamous cell carcinoma of the scrotum in HIV: two case reports

Abstract Background Squamous cell carcinoma (SCC) of the scrotum was the first malignancy known to be associated with exposure to an occupational carcinogen—in this case, soot trapped in the breeches of chimney sweeps. Better civil rules and regulations and the replacement of hearths with other form...

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Main Authors: Jeff John, Ken Kesner, John Lazarus
Format: Article
Language:English
Published: SpringerOpen 2021-06-01
Series:African Journal of Urology
Online Access:https://doi.org/10.1186/s12301-021-00177-3
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spelling doaj-107ef134b4374126a991b1e01b326fcf2021-06-13T11:26:08ZengSpringerOpenAfrican Journal of Urology1110-57041961-99872021-06-012711410.1186/s12301-021-00177-3Squamous cell carcinoma of the scrotum in HIV: two case reportsJeff John0Ken Kesner1John Lazarus2Division of Urology, Department of Surgery, Frere Hospital and Walter Sisulu UniversityDivision of Urology, Department of Surgery, Frere Hospital and Walter Sisulu UniversityDivision of Urology, Department of Surgery, Groote Schuur Hospital and University of Cape TownAbstract Background Squamous cell carcinoma (SCC) of the scrotum was the first malignancy known to be associated with exposure to an occupational carcinogen—in this case, soot trapped in the breeches of chimney sweeps. Better civil rules and regulations and the replacement of hearths with other forms of heating have rendered SCC of the scrotum a rarity. We report two cases of scrotal SCC with vastly differing clinical presentations and management. Case presentation Case 1 had T1 N0 M0 disease and presented with a small (< 2 cm), innocuous-looking, non-healing ulcer of eight years duration. A punch biopsy revealed a superficially invasive SCC confirmed on immunohistochemical profiling. A wide local excision of the lesion was subsequently performed. Follow-up at three years showed no signs of recurrence. Case 2 presented with T4 N1 M1 disease and rapidly progressing locally destructive mass. A punch biopsy of the scrotal lesion confirmed invasive moderately differentiated focally keratinising SCC. The metastatic evaluation confirmed the presence of metastatic, extensive para-aortic lymphadenopathy. He was managed with cisplatin-based chemoradiotherapy. Conclusion Early detection and management of patients with SCC of the scrotum are essential. If the diagnosis is delayed, treatment options become limited, and the prognosis is poor. Notwithstanding the rarity of this disease, multicentre trials are needed to provide more precise guidelines as to the optimal management of these patients.https://doi.org/10.1186/s12301-021-00177-3
collection DOAJ
language English
format Article
sources DOAJ
author Jeff John
Ken Kesner
John Lazarus
spellingShingle Jeff John
Ken Kesner
John Lazarus
Squamous cell carcinoma of the scrotum in HIV: two case reports
African Journal of Urology
author_facet Jeff John
Ken Kesner
John Lazarus
author_sort Jeff John
title Squamous cell carcinoma of the scrotum in HIV: two case reports
title_short Squamous cell carcinoma of the scrotum in HIV: two case reports
title_full Squamous cell carcinoma of the scrotum in HIV: two case reports
title_fullStr Squamous cell carcinoma of the scrotum in HIV: two case reports
title_full_unstemmed Squamous cell carcinoma of the scrotum in HIV: two case reports
title_sort squamous cell carcinoma of the scrotum in hiv: two case reports
publisher SpringerOpen
series African Journal of Urology
issn 1110-5704
1961-9987
publishDate 2021-06-01
description Abstract Background Squamous cell carcinoma (SCC) of the scrotum was the first malignancy known to be associated with exposure to an occupational carcinogen—in this case, soot trapped in the breeches of chimney sweeps. Better civil rules and regulations and the replacement of hearths with other forms of heating have rendered SCC of the scrotum a rarity. We report two cases of scrotal SCC with vastly differing clinical presentations and management. Case presentation Case 1 had T1 N0 M0 disease and presented with a small (< 2 cm), innocuous-looking, non-healing ulcer of eight years duration. A punch biopsy revealed a superficially invasive SCC confirmed on immunohistochemical profiling. A wide local excision of the lesion was subsequently performed. Follow-up at three years showed no signs of recurrence. Case 2 presented with T4 N1 M1 disease and rapidly progressing locally destructive mass. A punch biopsy of the scrotal lesion confirmed invasive moderately differentiated focally keratinising SCC. The metastatic evaluation confirmed the presence of metastatic, extensive para-aortic lymphadenopathy. He was managed with cisplatin-based chemoradiotherapy. Conclusion Early detection and management of patients with SCC of the scrotum are essential. If the diagnosis is delayed, treatment options become limited, and the prognosis is poor. Notwithstanding the rarity of this disease, multicentre trials are needed to provide more precise guidelines as to the optimal management of these patients.
url https://doi.org/10.1186/s12301-021-00177-3
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