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Radiotherapy for histiocytic sarcoma: A case report

  • Roswell Park Cancer Institute

Research output: Contribution to journalArticlepeer-review

1 Scopus citations

Abstract

Background Histiocystic sarcoma is a rare, but aggressive tumour that often involves extranodal sites. Histiocystic sarcoma is recognised by the World Health Organization as one of six subtypes of dendritic cell neoplasms. Diagnosis is difficult due to overlapping immunohistochemistry with other dendritic cell neoplasms. The optimal roles for chemotherapy, radiotherapy and surgery in the treatment of histiocytic sarcoma remain unknown. Methods We report a case of a patient with histiocytic sarcoma diagnosed after excisional biopsy and immunohistochemistry testing. Results The patient underwent external beam radiation therapy (EBRT). After 18 Gray (Gy), the 8 cm lesion had regressed to ~5 cm in diameter. The treatments were continued to a total dose of 45 Gy with the lesion regressing to less than a centimeter by the end of treatment. Local control was maintained but the patient died of acute myelogenous leukemia 5 months after her treatment. Conclusions This case suggests that histicytic sarcomas can be controlled locally with EBRT.

Original languageEnglish
Pages (from-to)212-215
Number of pages4
JournalJournal of Radiotherapy in Practice
Volume14
Issue number2
DOIs
StatePublished - Nov 21 2014

Keywords

  • dendritic cell
  • histiocytic sarcoma
  • lymphoma
  • radiation
  • S100 protein

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