Keywords
Renal-type clear cell carcinoma; prostate; transurethral resection; PSA levels; prostate adenocarcinoma; Gleason score.
This article is included in the Oncology gateway.
Renal-type clear cell carcinoma; prostate; transurethral resection; PSA levels; prostate adenocarcinoma; Gleason score.
Renal-type clear cell carcinoma (RTCCC) of the prostate was first described by Singh et al. in 2003,1,2 and, therefore, the literature describing this new, rare form of kidney cancer is very limited.3 Differential diagnosis of clear cell lesions in the prostate is challenging due to the multitude of conditions that could potentially underly the presenting symptoms. This includes clear cell variants of the more common adenocarcinoma of the prostate and urothelial carcinoma, along with rare clear cell carcinoma of Mullerian origin, metastatic renal cell carcinoma, and clear cell carcinoma of the prostate.4 We report a very rare case of a male with RTCCC of the prostate, in line with the updated consensus-based surgical case report (CARE) guidelines.5
An 81-year-old Buginese man who already underwent a cystostomy due to urine retention two weeks prior, was referred to our institution. The patient is a retired civil servant. His medical history included lower urinary tract symptoms and a trans urethral resection of the prostate (TURP) performed around eight months prior at a separate institution. Histopathological analysis indicated hyperplasia of the prostate and a digital rectal examination revealed that his enlarged prostate was hard in consistency and compressing the rectal wall. His serum markers and other biochemical parameters were all within the normal limits. Most importantly, his serum prostate-specific antigen (PSA) level was 23.01 ng/ml (normal value < 4 ng/ml). A hypoechoic lesion was found upon ultrasound examination, while both kidneys appeared healthy. Bone scans identified several osteoblast lesions on the inferior ramus of his bilateral pubic bone.
The patient underwent a urethrocystoscopy to evaluate his urethra and bladder followed by TURP. The resected tissue was histopathologically characterized as clear cell carcinoma and typical prostatic adenocarcinoma (Gleason score 3 + 4 = 7; Figure 1A). Immunohistochemistry showed areas immunoreactive to vimentin (VIM) (Figure 1B), epithelium membrane antigen (EMA) (Figure 1C), and membrane metalloendopeptidase, also known as cluster of differentiation 10 (CD-10) (Figure 1D).
A. Clear cell adenocarcinoma of the prostate. Cuboidal/hobnail cells, enlarged nuclei with mild pleomorphism (black arrow) (hematoxylin and eosin stain, 400× magnification). B. Positive immunostaining for vimentin (IHC, 400×). C. Positive immunostaining for EMA (epithelial membrane antigen) (IHC, 400×). D. Positive immunostaining for CD10 (IHC, 400×).
Bilateral subcapsular orchiectomy was chosen over medical hormonal therapy as the best suited treatment course for this patient. At the 12-month post-surgery follow-up, he reported that his lower urinary tract symptoms were nearly resolved and his serum PSA level was within the normal range (3.2 ng/ml).
RTCCC is associated with specific cytological morphologies, including atypical, enlarged, protruding nuclei, as well as classic structural features, like tubules, solid nests, or sheets in vascular-rich stroma with interstitial inflammatory infiltration.1 The most likely differential diagnosis is metastatic renal cell carcinoma to the prostate, for which, to the best of our knowledge, only two cases have been described in the literature.4
In the case described here, ultrasound examination found no abnormalities in both kidneys. Therefore, we concluded that the primary possible RTCCC lesion comes from the prostate. The immunohistochemical expression profile indicated that positive expressions of vimentin, EMA, and CD10 and significantly elevated serum levels of PSA indicated prostate malignancy. A mere seven reports have been published describing cases of prostate RTCCC. Collectively, the patients included in these studies were 42 to 73 years old, had PSA levels between 0.18 and 82 ng/mL, and Gleason scores above 6. The immunohistochemical results include positive expression of vimentin, EMA, CD10, low-molecular-weight cytokeratin, pan-cytokeratin, cytokeratin 7, paired box 8 (PAX8), prostatic specific acid phosphatase, periodic acid-Schiff, and alpha-methylacyl-coA racemase. Of the seven patients described in published case-reports of RTCCC of the prostate, five underwent radical prostatectomy and the remaining two received TURP. Local recurrence in the pelvis was apparent 24 months after radical cystoprostatectomy in one patient and two patients died due to multi-organ failure (6 months after TURP and 29 months after radical cystoprostatectomy).3,4,6
The treatment of RTCCC of the prostate is similar to that used to combat the more common forms of prostate cancer.1–4,6 In the present case, bone scans revealed skeletal metastases at the inferior ramus of his bilateral pubic bone. After explaining the advantages and disadvantages of bilateral subcapsular orchiectomy and medical hormonal therapy, the patient chose the former, since the latter would require frequent trips to the outpatient department, which was problematic given how far he lives from the hospital and his limited access to transportation.
This case study of a patient with RTCCC of the prostate supports that this new, rare pathological entity is characterized by histological and immunohistochemical profiles similar to renal clear cell carcinoma. Accurate differential diagnosis, e.g., distinguishing RTCCC from clear cell urothelial carcinoma and metastatic clear cell renal cell carcinoma, remains a pressing concern that warrants further investigation to optimize treatment selection and patient outcome.
All data underlying the results are available as part of the article and no additional source data are required.
Written informed consent for publication of their clinical details and/or clinical images was obtained from the patient.
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Is the background of the case’s history and progression described in sufficient detail?
Yes
Are enough details provided of any physical examination and diagnostic tests, treatment given and outcomes?
Partly
Is sufficient discussion included of the importance of the findings and their relevance to future understanding of disease processes, diagnosis or treatment?
Yes
Is the case presented with sufficient detail to be useful for other practitioners?
Partly
Competing Interests: No competing interests were disclosed.
Reviewer Expertise: Urology, Immunology, Kidney Transplant, Oncology, Precision Medicine, Health Economic, Systematic Review, Surgery, Nephrology
Is the background of the case’s history and progression described in sufficient detail?
Yes
Are enough details provided of any physical examination and diagnostic tests, treatment given and outcomes?
Yes
Is sufficient discussion included of the importance of the findings and their relevance to future understanding of disease processes, diagnosis or treatment?
Yes
Is the case presented with sufficient detail to be useful for other practitioners?
Yes
Competing Interests: No competing interests were disclosed.
Reviewer Expertise: Urology; pediatric urology, endourology, basic research, laparoscopy.
Alongside their report, reviewers assign a status to the article:
Invited Reviewers | ||
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Version 1 15 Jun 21 |
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