AB013. Management of germ cell tumors: a case with growing teratoma syndrome

Abstract

: The growing teratoma syndrome in patients with anterior mediastinal germ cell tumors were rare. Here, we report a patient with primary anterior mediastinal malignant mixed germ cell tumor that exhibited growing teratoma syndrome after initiation chemotherapy. A 28-year-old man is admitted to the hospital complaining of dyspnea. Chest computed tomography (CT) showed a huge heterogeneous anterior mediastinal mass (20 cm in longest direction). The tumor compressed the left lung, heart and great vessels. The α-fetoprotein (AFP) is higher than 3,000 ng/mL, the β-human chorionic gonadotropin (β-HCG) level is increased to 49.7 ng/mL. Core-needle biopsy confirmed the diagnosis of teratoma with nonseminomatous germ cell tumors. The patient was administered two rounds of bleomycin, etoposide, cisplatin (BEP) chemotherapy, but the mass grew despite Serum AFP was rapidly declining (171 ng/mL). And CT scan revealed a notable enlargement of the tumor. Surgical tumor resection was performed through a median sternotomy. The tumor was adherent to the pericardium, bilateral mediastinum pleura, left upper lobe, and left phrenic nerve. The tumor was completely resected including pericardiectomy, resection of the left phrenic nerve, and left upper lobectomies. The pathologic examination revealed malignant mixed germ cell tumor with extensive areas of chemotherapy-induced necrosis which was consisted with mature teratoma, immature teratoma and embryonal carcinoma. The patient was alive without recurrence at 6 months after two rounds of adjuvant chemotherapy.