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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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 |
work_keys_str_mv |
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