Abstract | BACKGROUND: Infantile myofibromatosis (IM) is a rare benign tumor of infancy. Cases with solitary and multicentric disease usually spontaneously regress, but multicentric disease with visceral involvement carries a poor prognosis. Few cases of multicentric disease with central nervous system (CNS) involvement have been reported, and none report survival. OBSERVATIONS: We present a newborn with multicentric IM with cutaneous, visceral, and CNS involvement. She was treated with vinblastine, methotrexate, and the novel addition of intrathecal methotrexate with treatment response after 1 year of therapy. CONCLUSIONS: Multicentric IM with CNS involvement can be successfully treated with a multimodal approach of chemotherapy with the addition of intrathecal methotrexate and surgery.
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Authors | Stephanie Gehle, Carolyn Quinsey, Diana McShane, Patrick Thompson, Gerardo Quezada |
Journal | Journal of pediatric hematology/oncology
(J Pediatr Hematol Oncol)
Vol. 45
Issue 7
Pg. e921-e923
(10 01 2023)
ISSN: 1536-3678 [Electronic] United States |
PMID | 37526359
(Publication Type: Journal Article)
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Copyright | Copyright © 2023 Wolters Kluwer Health, Inc. All rights reserved. |
Chemical References |
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Topics |
- Infant, Newborn
- Female
- Humans
- Methotrexate
(therapeutic use)
- Myofibromatosis
(therapy, pathology)
- Vinblastine
(therapeutic use)
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