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Successful Treatment of Relapsed Disseminated Juvenile Xanthogranuloma with Central Nervous System Involvement

Year: 2024
Type: article
Study design: Case Report
Abstract: Juvenile xanthogranuloma (JXG) is a rare histiocytic disorder primarily affecting children, typically presenting as self-limiting skin lesions.However, extracutaneous JXG (extra-JXG) or systemic JXG (sJXG) can involve various organs, including the central nervous system (CNS), leading to high morbidity and mortality, especially in cases of CNS involvement.Treatment approaches for CNS-JXG, including surgical resection, chemotherapy, and radiation therapy, lack consensus, with reports of relapsed or refractory cases being rare.Here, we present the case of a 2-year-old girl with refractory extra-JXG involving the CNS, characterized by multiple intracranial lesions.Initial chemotherapy with prednisolone and vinblastine showed no response, and second-line therapy, including cytarabine and vincristine combined with surgical resection, was also ineffective.However, a 6-cycle third-line chemotherapy regimen incorporating vincristine and carboplatin led to a positive response, with stable disease status, and normal growth and neurodevelopment observed.Our findings suggest that combined chemotherapy with carboplatin and vincristine is a feasible and well-tolerated treatment strategy for patients with CNS-JXG.
Language: English
Subfield: Physiology
Field: Medicine
Open Access status: diamond
OpenAlex ID: W4403848175
FWCI: 0.239
Cites: 14
Cited by: 1
Related to: 10