Mesonephric (Wolffian-derived) Adenocarcinoma of the Female Urethra
| Autor: | Gladell P. Paner, Mahul B. Amin, Antonio Lopez-Beltran |
|---|---|
| Rok vydání: | 2020 |
| Předmět: |
Pathology
medicine.medical_specialty business.industry 030232 urology & nephrology medicine.disease Pathology and Forensic Medicine Metastasis Mesonephric duct 03 medical and health sciences 0302 clinical medicine Urethra medicine.anatomical_structure 030220 oncology & carcinogenesis medicine Adenocarcinoma Surgery Nuclear atypia Anatomy Mesonephric Remnants Clear-cell adenocarcinoma business Clear cell |
| Zdroj: | American Journal of Surgical Pathology. 45:543-549 |
| ISSN: | 0147-5185 |
| DOI: | 10.1097/pas.0000000000001635 |
| Popis: | The current World Health Organization (WHO) classification of adenocarcinoma of the urinary tract including the urethra includes uncommon Mullerian-derived carcinomas such as clear cell and endometrioid adenocarcinomas. The concept of primary mesonephric (Wolffian-derived) adenocarcinoma (MA) in the urethra (and urinary tract in general) is currently regarded as controversial as the term "mesonephric" had been also inaccurately applied in the past to label Mullerian-derived carcinomas, particularly clear cell adenocarcinoma. Further, pathologically well-documented or bona fide urethral MAs have not yet to be reported. Herein, we describe 2 examples of MA in elderly females that primarily presented in the urethra and manifested clinically with obstructive lower urinary tract symptoms. Both tumors exhibited histology similar to those in MAs of the female genital tract including the distinctive tubular proliferations with luminal eosinophilic materials. The first case, in addition, showed a variety of patterns including ductal (glandular), solid, fused/sieve-like tubules, dilated tubules, and spindled cells. The second case also showed a transition to the more irregular and poorly formed tubular proliferation of cells with greater nuclear atypia and with a desmoplastic response. Both tumors showed positivity for PAX8, GATA3, and luminal CD10, and 1 tumor analyzed harbored KRAS and ARID1A mutations. One patient received neoadjuvant chemotherapy and underwent resection but had local tumor recurrence and metastasis to the lungs and lumbar spine 12 months after presentation. In conclusion, MA, similar to those occurring in the female genital tract and distinct from the recognized Mullerian-derived carcinomas, may present primarily as urethral tumors. MA in the urethra probably shares a common pathogenesis with vaginal MA as both may originate from the same caudal loci of mesonephric remnants along the closely apposed anterior vaginal and posterior urethral walls. MA should be considered in future classifications for urethral tumors and we recommend that the confusing term "mesonephroid adenocarcinoma" should no longer be used. |
| Databáze: | OpenAIRE |
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