Difference between revisions of "WSI24-411-Case-4"
From MGH Learn Pathology
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|performer=Jt026 | |performer=Jt026 | ||
|reasonCode=37 y.o. man with a history of testicular GCT containing teratoma, “somatic-type” RMS and ENET s/p orchiectomy + RPLND. Developed post-orchiectomy/RPLND recurrence treated with Etoposide + cisplatin + ifosfamide followed by Copanlesib (tumor showed a pathogenic PIK3CA variant). A complex multiorgan resection is performed to excise a large residual retroperitoneal mass. | |reasonCode=37 y.o. man with a history of testicular GCT containing teratoma, “somatic-type” RMS and ENET s/p orchiectomy + RPLND. Developed post-orchiectomy/RPLND recurrence treated with Etoposide + cisplatin + ifosfamide followed by Copanlesib (tumor showed a pathogenic PIK3CA variant). A complex multiorgan resection is performed to excise a large residual retroperitoneal mass. | ||
| − | |supportingInfo= | + | |supportingInfo=Low grade glial tumor of germ cell origin (likely maturation of ENT) |
|identifier=WSI24-411-Case-4 | |identifier=WSI24-411-Case-4 | ||
|access=Public | |access=Public | ||
Latest revision as of 20:50, February 12, 2026
