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Malignant triton tumor of the rectum - A case report and review of the literature.
Herzberg, J; Corradini, G M; von Seydewitz, C; Guraya, S Y; Strate, T; Honarpisheh, H.
Afiliación
  • Herzberg J; Department of Surgery, Hospital Reinbek St. Adolf Stift, Germany. Electronic address: jonas.herzberg@Krankenhaus-Reinbek.de.
  • Corradini GM; Institute of Hematopathology Hamburg, Hamburg, Germany.
  • von Seydewitz C; Department of Oncology, Hospital Reinbek St. Adolf Stift, Germany.
  • Guraya SY; Clinical Sciences Department, College of Medicine, University of Sharjah, United Arab Emirates.
  • Strate T; Department of Surgery, Hospital Reinbek St. Adolf Stift, Germany.
  • Honarpisheh H; Department of Surgery, Hospital Reinbek St. Adolf Stift, Germany.
Int J Surg Case Rep ; 76: 517-521, 2020.
Article en En | MEDLINE | ID: mdl-33207422
ABSTRACT

INTRODUCTION:

Malignant triton tumors (MTT) are rare but highly aggressive tumors that originate from the Schwann cells. These tumors can occur in any part of the body, mostly present late and carry poor prognosis. PRESENTATION OF CASE We present a 24-year-old man with a rectal MTT causing non-specific abdominal pain and recurring ileus. The MRI showed a rectal mass near the urinary bladder with compression on the seminal vesical. A complete surgical resection of the tumor was performed. The immunohistological report confirmed a rectal MTT. Because of persistent ileus during the post-operative palliative chemotherapy, another tumor debulking was performed. The patient died 9 months after the diagnosis of MTT due to local recurrence under chemotherapy. DISCUSSION AND

CONCLUSION:

MTTs are uncommon tumors in young age with high morbidity and mortality because of local recurrence also after complete resection.
Palabras clave

Texto completo: 1 Bases de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: Int J Surg Case Rep Año: 2020 Tipo del documento: Article

Texto completo: 1 Bases de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: Int J Surg Case Rep Año: 2020 Tipo del documento: Article