Successful Salvage Treosulfan-Based Megachemotherapy With Allogeneic Stem Cell Transplantation in Nonsyndromic, Therapy-Resistant Disseminated Juvenile Xanthogranuloma: A Case Report

Juvenile xanthogranuloma (JXG) is a rare histiocytic disorder classified as non-Langerhans cell histiocytosis; although it is usually a benign and self-limiting disease, it can be fatal in some cases, especially with systemic dissemination. We present a case report of a boy with therapy-resistant di...

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Published in:Transplantation proceedings Vol. 52; no. 9; pp. 2844 - 2848
Main Authors: Janeczko-Czarnecka, Małgorzata, Raciborska, Anna, Gos, Monika, Kordowska, Olga, Gajek, Kornelia, Rybka, Blanka, Ryczan-Krawczyk, Renata, Kałwak, Krzysztof, Ussowicz, Marek
Format: Journal Article
Language:English
Published: United States Elsevier Inc 01-11-2020
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Summary:Juvenile xanthogranuloma (JXG) is a rare histiocytic disorder classified as non-Langerhans cell histiocytosis; although it is usually a benign and self-limiting disease, it can be fatal in some cases, especially with systemic dissemination. We present a case report of a boy with therapy-resistant disseminated JXG who was treated with systemic chemotherapy and received 3 allogeneic hematopoietic stem cell transplantations (allo-HSCTs) from an unrelated donor. The post-transplant period was complicated by acute graft vs host disease and lymphoproliferative disease caused by Epstein-Barr virus. Currently, almost 7.5 years after the first transplantation, the boy is in complete remission with full donor chimerism and without symptoms of JXG. The presented data confirm rare observations that allo-HSCT can lead to durable remission of systemic JXG, which warrants its use in life-threatening, therapy-resistant subtypes of disease. •Allogeneic hematopoietic stem cell transplantations (allo-HSCT) can lead to durable remission of systemic juvenile xanthogranuloma.•Treosulfan-melphalan regimen shows efficacy in juvenile xanthogranuloma.•Intrathecal rituximab can be used for lymphoproliferative disease of the central nervous system.
ISSN:0041-1345
1873-2623
DOI:10.1016/j.transproceed.2020.05.025