Testicular Malignancy: A Case Study

Decent Essays
Role and indications of RPLND in Testicular Malignancy
• RATIONALE IN STAGE I NSGCT: Surveillance is preferred for low risk stage I NSGCT compliant patient. High risk features include lymphovascular invasion, predominant embryonal component (>40%) and/or higher T stage (T2-T4) [30,31]. Patients with these high risk features have options of either one or two cycles of single agent platin or primary RPLND. Concern regarding long-term morbidities of imaging related ionizing radiation exposure and long term morbidities of chemotherapy, have emphasized the importance of surgery [32,33]. Advantages of RPLND include 1) definitive pathologic staging. 30% of stage I patients have occult metastasis in the retroperitoneum and 35% of patients with stage
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Resection of residual tumors after first line chemotherapy remains essential in the treatment of metastatic testicular cancer. Undifferentiated tumor may still be found in 20%. Necrosis is found in only 50% of marker normalized patients after first-line and approximately 30% after second-line chemotherapy [38]. The histological outcomes of patients after induction chemotherapy followed by Postchemotherapy RPLND revealed 45% fibrosis, 40% teratoma, and 15% viable tumor and after seconding chemotherapy, specimens revealed approximately 50% malignant GCT, 40% teratoma, and 10% fibrosis [39]. Bilateral RPLND with nerve sparing if possible is the preferred management as it provide definitive diagnosis, eliminate possibility of growing teratoma syndrome and malignant transformation of teratoma which occur in 3-6% and increase to 12-18% in late relapses [40,41,42].
• RATIONALE FOR SEMINOMA: advanced stage residual masses greater than 3 cm should be evaluated further with FDG-PET andPET positive should undergo RPLND. Observation is justified in patients with a negative FDGPET scan after primary chemotherapy, particularly for those with residual masses less than 3 cm

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