Literature DB >> 8037350

Successful treatment of multisystem Langerhans cell histiocytosis (histiocytosis X) with etoposide.

L C Yu1, S Shenoy, K Ward, R P Warrier.   

Abstract

PURPOSE: Langerhans cell histiocytosis (LCH) in its disseminated form usually occurs in the very young, and has a fulminant, rapidly progressive, and fatal course despite different forms of therapy. PATIENTS AND METHODS: We treated two patients, who had failed on vinblastine treatment, with i.v. etoposide (VP-16) at a dose of 150 mg/kg/day for 3 days. Patient I, 8 months of age, presented with failure to thrive and huge bilateral granulomatous lesions of the external auditory canal with erosion and extensive destruction of the petrous pyramids and mastoid area. Patient II, 20 months of age, presented with widespread purpuric skin rash, hepatosplenomegaly, and bone marrow involvement.
RESULTS: Both patients sustained complete remission (CR) following three to six courses of VP-16 and continued to be in unmaintained CR for > 48 months from diagnosis. No major toxicity was noted.
CONCLUSIONS: Etoposide (VP-16), an epipodophyllotoxin known for its usefulness in the treatment of malignancies of the monocyte/macrophage lineage, appears to be an effective treatment for the severe multisystem (disseminated) LCH of childhood and should be strongly considered as front-line therapy for this subgroup of patients with poor prognostic factors.

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Year:  1994        PMID: 8037350     DOI: 10.1097/00043426-199408000-00017

Source DB:  PubMed          Journal:  Am J Pediatr Hematol Oncol        ISSN: 0192-8562


  1 in total

1.  A Case of Langerhans Cell Histiocytosis Manifested as a Suprasellar Mass.

Authors:  Ju Young Yoon; Byung-Kiu Park; Heon Yoo; Sang Hyun Lee; Eun Kyung Hong; Weon Seo Park; Young Joo Kwon; Jong Hyung Yoon; Hyeon Jin Park
Journal:  Brain Tumor Res Treat       Date:  2016-04-29
  1 in total

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