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Infantile myofibromatosis
Margarita Larralde1,2, Bruno Ferrari1, Juan Pablo Martinez1
1Pediatric Dermatology Section, Hospital Ramos Mejía, Buenos Aires, Argentina.
Insights
Infantile myofibromatosis, a common childhood fibrous tumor, can affect skin and bone. A newborn with this condition responded well to vinblastine and methotrexate treatment.
Area of Science:
- Pediatric Oncology
- Dermatopathology
- Skeletal Dysplasias
Background:
- Infantile myofibromatosis is the most common fibrous tumor in childhood.
- It is a mesenchymal disorder involving fibrous proliferation in various tissues.
- This condition can manifest in the skin, bone, muscle, and viscera.
Observation:
- A case report of a newborn presenting with infantile myofibromatosis.
- The newborn exhibited involvement of the skin and bone.
- Importantly, there was no visceral organ involvement.
Findings:
- The newborn demonstrated a positive therapeutic response to a combination of vinblastine and methotrexate.
- This suggests potential efficacy of chemotherapy in specific presentations of infantile myofibromatosis.
- The case highlights a non-visceral form of the disease.
Implications:
- This case contributes to understanding the clinical spectrum of infantile myofibromatosis.
- It underscores the importance of considering chemotherapy in managing non-visceral infantile myofibromatosis.
- Further research into targeted therapies for infantile myofibromatosis is warranted.
Abstract:
Infantile myofibromatosis is a mesenchymal disorder characterized by the fibrous proliferation of the skin, bone, muscle and viscera. It is the most common fibrous tumor in childhood. We present a newborn with skin and bone disease without visceral involvement, who showed good response to vinblastine and methotrexate. Clinical features, etiology, diagnosis, and treatment are reviewed.
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