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The Journal of Thoracic and Cardiovascular Surgery, Vol 89, 826-835, Copyright © 1985 by The American Association for Thoracic Surgery and The Western Thoracic Surgical Association
EE Lack, HJ Weinstein and KJ Welch
Twenty-one patients aged 16 years or less had been treated for a primary
mediastinal germ cell tumor at the Children's Hospital, Boston
Massachusetts, during the last 54 years. There were 13 boys and eight girls
with the average age at diagnosis being 7 years (range 2 weeks to 16
years). Twelve mediastinal germ cell tumors were classified as pure
teratoma, five contained embryonal carcinoma admixed with other germ cell
components, and four were pure embryonal carcinoma. Of 12 patients with
pure teratoma, 10 underwent complete surgical resection and were alive and
well 1 to 13 years later; two children left untreated died of complications
related to local tumor growth. Complete surgical resection was possible for
only two of nine patients with embryonal carcinoma; both received adjuvant
therapy and were alive and well 3 and 20 years later. Seven patients
received radiation and/or chemotherapy but died of residual or metastatic
disease. Successful treatment for children with embryonal carcinoma
requires an operation aimed at either debulking or complete resection (if
possible) coupled with early and aggressive combination chemotherapy. The
role of radiation in primary therapy remains undefined with regard to
curative intent.
ARTICLES
Mediastinal germ cell tumors in childhood. A clinical and pathological study of 21 cases
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