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Prostatic marker-negative amphicrine carcinoma of the prostate
J C Papadimitriou1, R R Weihing, C Choi
1Department of Pathology, School of Medicine, University of Maryland, Baltimore.
Ultrastructural Pathology
|May 1, 1994
Summary
This study details a rare case of metastatic prostate cancer lacking typical prostate markers but showing significant neuroendocrine features. Findings support the link between poor tumor differentiation and neuroendocrine expression in prostate carcinoma.
Area of Science:
- Oncology
- Pathology
- Cancer Biology
Background:
- Prostate adenocarcinoma differentiation typically correlates with prostatic-specific marker and neuroendocrine expression.
- Undifferentiated tumors show decreased prostatic markers and increased neuroendocrine cells, often associated with small cell morphology.
- Previous reports link complete absence of prostatic markers and marked neuroendocrine expression to small cell carcinoma.
Observation:
- This report describes a unique case of metastatic, prostatic marker-negative, non-small cell prostate adenocarcinoma with a prominent neuroendocrine component.
- Luminal-exocrine cells appeared ultrastructurally undifferentiated with sparse cytoplasm, contrasting with controls.
- Neuroendocrine cells, identified as eosinophilic cells, were significantly increased in metastatic foci compared to the primary tumor.
Findings:
- The neuroendocrine cells observed differed ultrastructurally from previously reported Paneth-like cells in prostate carcinoma.
- This case supports the concept of multidirectional differentiation in epithelial cancers.
- A strong association between poor tumor differentiation and neuroendocrine expression in prostate carcinoma is further supported.
Implications:
- The findings challenge the typical association of neuroendocrine expression solely with small cell prostate carcinoma.
- The presence of well-formed basal laminae in metastatic foci contrasts with prior observations.
- This case highlights the complexity of prostate cancer differentiation and potential therapeutic targets.