Literature DB >> 25986270

Neuroendocrine carcinoma arising in a mediastinal teratoma with pulmonary metastasis: a case report and the chemotherapy response.

So Yeon Lee1, Young Min Jo, Jaehee Lee, Seung Ick Cha, Tae In Park, Chang Ho Kim.   

Abstract

Neuroendocrine carcinoma as a somatic-type malignancy (STM) arising in an extragonadal teratoma is extremely rare. The effect of chemotherapy has been poorly evaluated in such cases contrary to teratomas with other STMs. We herein demonstrate that systemic chemotherapy may be beneficial in a case of neuroendocrine carcinoma arising in a mediastinal teratoma with pulmonary metastasis. A 31-year-old man presented with mediastinal widening visualized on a chest radiograph. Computed tomography showed a huge mediastinal mass with two pulmonary nodules. Surgical resection confirmed the presence of a neuroendocrine carcinoma arising in a mediastinal teratoma and pulmonary metastasis. The patient subsequently received chemotherapy and has had no recurrence during the 28-month follow-up.

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Year:  2015        PMID: 25986270     DOI: 10.2169/internalmedicine.54.3947

Source DB:  PubMed          Journal:  Intern Med        ISSN: 0918-2918            Impact factor:   1.271


  2 in total

1.  Growing Teratoma Syndrome a Rare Clinical Entity: Two Decades Management Experience from the Regional Cancer Institute.

Authors:  Praveen S Rathod; Amarinder Singh; R M Punyashree; V R Pallavi; A Usha; C R Vijay; K Shoba; K Rajshekar
Journal:  Indian J Surg Oncol       Date:  2020-09-23

2.  Mediastinal Teratoma with Neuroendocrine Features in 34-Year-Old Male with Syncope.

Authors:  Peter A Andrawes; Masood A Shariff; Qing Chang; Fanyi Kong; Frank M Rosell
Journal:  Case Rep Surg       Date:  2015-12-10
  2 in total

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