Growing Teratoma Syndrome in the Setting of Sarcoidosis: A Case Report and Literature Review.
Adel ShahnamRobyn SayerUnine HerbstRaghwa SharmaWon-Hee YoonTim DinihanBo GaoPublished in: Current oncology (Toronto, Ont.) (2022)
Growing teratoma syndrome (GTS) is rare and can mimic disease recurrence in patients with a history of immature teratoma. Benign hypermetabolic lymphadenopathy found on staging and surveillance computed tomography (CT) and positron emission tomography (PET) may lead to the presumption of metastatic malignancy. We report a case of a 38 year old with mixed mature and immature teratomas who developed new peritoneal masses after adjuvant chemotherapy despite a normalization of tumor markers. In addition to low FDG uptake observed in these peritoneal masses, a PET scan showed hypermetabolic lymphadenopathy and pulmonary and spleen lesions suggesting widespread metastases. Subsequent surgical resection confirmed a mixed pathology with GTS and sarcoidosis. We reviewed the current literature evidence of GTS and sarcoidosis as a benign cause of lymphadenopathy in cancer patients. We emphasize the importance of a tissue diagnosis before instituting therapy for presumed cancer recurrence to avoid potentially fatal diagnostic traps and management errors. A multiple disciplinary team approach is imperative in managing patients with suspected recurrent immature teratomas.
Keyphrases
- positron emission tomography
- computed tomography
- fine needle aspiration
- contrast enhanced
- pet ct
- ultrasound guided
- dual energy
- pet imaging
- image quality
- magnetic resonance imaging
- systematic review
- papillary thyroid
- free survival
- squamous cell carcinoma
- small cell lung cancer
- public health
- pulmonary hypertension
- lymph node
- magnetic resonance
- patient safety
- palliative care
- quality improvement
- emergency department
- young adults