Mediastinal Growing Teratoma Syndrome Succesfully Treated by Multiple Modality Therapies

6Citations
Citations of this article
14Readers
Mendeley users who have this article in their library.

Abstract

A 43-year-old-man was diagnosed as having primary mediastinal nonseminomatous germ cell tumor based on pericutaneous biopsy and an elevated serum concentration of alpha-fetoprotein (AFP). Although AFP decreased after chemotherapy, the mass size grew and developed tracheal compression by the tumor. The patient was treated with mechanical ventilation and subsequent stent implantation for keeping airway patency. After three cycles of chemotherapy and normalization of AFP, the increased mass was successfully resected and the pathological examination demonstrated a mature teratoma. This case showed a rare clinical manifestation of mediastinal growing teratoma syndrome and successful outcome by multimodal therapies. © 2011, The Japanese Society of Internal Medicine. All rights reserved.

Cite

CITATION STYLE

APA

Agatsuma, T., Koizumi, T., Kubo, K., Saito, G., Kondo, R., Yoshida, K., … Shimojo, H. (2011). Mediastinal Growing Teratoma Syndrome Succesfully Treated by Multiple Modality Therapies. Internal Medicine, 50(6), 607–610. https://doi.org/10.2169/internalmedicine.50.4653

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free