Malignant peripheral nerve sheath tumor historical perspective: Difference between revisions

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==Historical Perspective==
==Historical Perspective==
*In 18th century, NF1-like cutaneous tumor syndromes appeared in the literature.
*In 18th century, NF1-like cutaneous tumor syndromes appeared in the literature.
*In 1880s, Friedrich von Recklinghausen published seminal observations detailing cutaneous tumors comprised of both neuronal and fibroblastic tissue finally termed as neurofibromas.


==References==
==References==

Revision as of 13:26, 16 August 2019

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Marjan Khan M.B.B.S.[2]

Overview

NF1-like cutaneous tumor syndromes appeared in the literature in 1880s, when Friedrich von Recklinghausen published seminal observations detailing cutaneous tumors comprised of both neuronal and fibroblastic tissue finally termed as neurofibromas. In 2006, Yang et al demonstrated a critical neurofibroma microenvironment interaction that includes SCF-stimulated Nf1+/− mast cells potentiating Nf1+/− fibroblast functions.

Historical Perspective

  • In 18th century, NF1-like cutaneous tumor syndromes appeared in the literature.
  • In 1880s, Friedrich von Recklinghausen published seminal observations detailing cutaneous tumors comprised of both neuronal and fibroblastic tissue finally termed as neurofibromas.

References

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