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Extracellular signal-regulated kinase activation of self-healing Langerhans cell histiocytosis: A case report. | LitMetric

AI Article Synopsis

  • A 3-month-old boy developed small papules on his trunk, prompting a diagnosis of Langerhans cell histiocytosis after pathological examination.
  • Initially, the papules were isolated to his skin with no organ involvement, classified as single-system, skin-limited LCH.
  • Treatment with topical steroids led to regression of the skin rashes, with all papules disappearing by 6 months, and involved understanding the role of genetic mutations, especially in the BRAF gene, contributing to the condition's development.

Article Abstract

A 3-month-old boy developed small papules on his trunk. After the papules increased in number, the patient was diagnosed with Langerhans cell histiocytosis based on the pathological findings. He was referred to our department for further examination. Upon initial examination, the papules and nodules were scattered on his back, abdomen and lumbar region. Because he did not present with any organ involvement except the skin, he was diagnosed with single-system and skin-limited Langerhans cell histiocytosis. Skin rashes were treated with a topical steroid and started regressing 3 months after onset. All papules disappeared 6 months after onset. In this boy, the Langerhans cell histiocytosis tumor cells expressed phosphorylated extracellular signal-regulated kinases. In Langerhans cell histiocytosis, BRAF V600E and other genes are known to mutate to act as driver mutations in stem cells of the myeloid dendritic cell lineage. Consequently, extracellular signal-regulated kinases are continuously activated, which contributes to Langerhans cell histiocytosis carcinogenesis.

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Source
http://dx.doi.org/10.1111/1346-8138.14996DOI Listing

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