“…1 CTT is most likely underdiagnosed, since it is often focal and mixed within teratoma components, most frequently found in the setting of postchemotherapy retroperitoneal lymph-node dissections (pcRPLND), 1 but also, albeit rarely, in metastatic chemo-na€ ıve patients, 2 as part of primary testicular germ cell tumours (TGCT), 3 and recently in the setting of a primary central nervous system germ cell tumour. 4 Its pathogenesis is poorly understood, and two theories have been proposed: regression of choriocarcinoma under chemotherapy, explaining the event in pcRPLND cases, and spontaneous regression, justifying the event in untreated patients. The fact that CTT is almost always associated with teratoma raised the hypothesis that this morphology represents a late phase in maturation towards teratoma.…”