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Article

Coincidental Expression of Classic Hodgkin Lymphoma and Neurofibromatosis Type I and Literature Review.

Journal of pediatric hematology/oncology - 1 May 2021

Cabrera Trevor B, Wang Wei, Yedururi Sireesha, Slopis John M, Steiner Raphael E, Rytting Michael E, Cuglievan Branko

Abstract excerpt

Neurofibromatosis Type 1 (NF1) is a genetic disorder with an incidence of 1 in 2600 to 3000 individuals. It is a clinical diagnosis characterized by café-au-lait macules, neurofibromas, and axillary and/or groin freckling. Because of genetic mutations in the NF1 gene affecting the Ras/mitogen-activated protein kinase pathway, there is also risk of associated soft tissue sarcomas and hematologic malignancies....

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Identifiers

PMID: 32366782
DOI: 10.1097/MPH.0000000000001811

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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