Ontology highlight
ABSTRACT: Background
The article discusses a rare case of a giant immature teratoma (IMT) in an infant, highlighting the challenges in diagnosing and managing this type of germ cell tumor that arises from abnormal embryonic cell development. Teratoma growth syndrome represents a rare clinical manifestation, posing significant challenges in differential diagnosis, particularly when distinguishing it from peritoneal gliomatosis or progressive germinoma. In essence, growing teratoma syndrome (GTS) constitutes a distinct and intricate clinical entity that requires meticulous monitoring and management to enhance patient outcomes.Case description
The patient was a male infant, presented with a palpable mass in the upper abdomen at 4 months of age. Initial ultrasound and elevated serum alph
SUBMITTER: Song Y
PROVIDER: S-EPMC12319614 | biostudies-literature | 2025
REPOSITORIES: biostudies-literature