Postpubertal-Type Teratoma of the Retroperitoneal Space as a Late Recurrence of a Testicular Germ Cell Tumor: A Case Report With Clinical Insight
Postpubertal-type teratomas are rare malignant tumors derived from germ cell neoplasia in situ (GCNIS). This case report presents a rare instance of a retroperitoneal postpubertal-type teratoma as a late recurrence of a testicular germ cell tumor (GCT) that was initially diagnosed as a seminoma. A 4...
Gespeichert in:
Veröffentlicht in: | Curēus (Palo Alto, CA) CA), 2024-10, Vol.16 (10), p.e71667 |
---|---|
Hauptverfasser: | , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | Postpubertal-type teratomas are rare malignant tumors derived from germ cell neoplasia in situ (GCNIS). This case report presents a rare instance of a retroperitoneal postpubertal-type teratoma as a late recurrence of a testicular germ cell tumor (GCT) that was initially diagnosed as a seminoma. A 48-year-old male who had undergone left inguinal orchidectomy for a testicular mass was diagnosed with a seminoma (stage I) six years prior and presented with an asymptomatic 6-cm retroperitoneal tumor near the left renal hilum. Initial blood tests at presentation for the retroperitoneal tumor were normal, except for a mild elevation of lactate dehydrogenase. Computed tomography (CT), magnetic resonance imaging, and fluorine-18-fluorodeoxyglucose positron emission tomography (18F-FDG PET)/CT imaging revealed a well-defined tumor with calcification and high glucose metabolic activity. A CT-guided biopsy for the retroperitoneal tumor suggested a high-grade malignant tumor of neuroendocrine origin. The patient underwent neoadjuvant chemotherapy, which resulted in tumor shrinkage and decreased metabolic activity. Subsequent surgical resection and histopathological examination revealed a postpubertal-type teratoma with a concomitant neuroendocrine tumor. A reexamination of the previous testicular tumor specimen revealed a small amount of embryonal carcinoma within the seminoma, indicating that the initial diagnosis should have been a mixed germ cell tumor rather than a pure seminoma. This explains the unusual recurrence pattern observed and highlights the importance of a thorough histological examination for testicular GCTs, as microscopic non-seminomatous components can significantly affect prognosis and recurrence patterns. When encountering suspected recurrences of GCNIS-derived GCTs, clinicians should consider the possibility of an initially undetected mixed GCT, particularly in cases with atypical presentation or recurrence patterns. |
---|---|
ISSN: | 2168-8184 2168-8184 |
DOI: | 10.7759/cureus.71667 |