Rare MYC -amplified Neuroblastoma With Large Cell Histology
Year: 2018
Type: article
Study design: Case Report
Abstract: Background Although MYCN (aka N-myc) amplification is reported in ∼20% of neuroblastomas, MYC (aka C-myc) amplification appears to be a rare event in this disease. As of today, only 2 MYC-amplified neuroblastomas have been briefly mentioned in the literature. Methods We studied here the clinicopathological features of 3 MYC-amplified neuroblastomas. Results All 3 patients (2 females and 1 male) had stage 4 disease. One female is currently alive and well 52 months after the diagnosis, while the other female and male patients died of disease 24 and 20 months after the diagnosis, respectively. Further analysis on 2 tumors revealed unfavorable histology with MYC protein overexpression but with neither MYCN amplification nor MYCN protein overexpression. Both of these tumors exhibited "large cell neuroblastoma" histology with enlarged, uniquely open nuclei and nucleolar hypertrophy, along with "aberrant" desmin expression. Conclusions MYC-amplified neuroblastomas are extremely rare and seem to present with distinct clinicopathological features.
Institutions: Children's Hospital Los Angeles, UNSW Sydney, Prince of Wales Hospital, Kaiser Permanente, Kaiser Permanente San Francisco Medical Center, St Vincent's Hospital Melbourne, St Vincent's Hospital Sydney, Sydney Children's Hospital, Saiseikai Takaoka Hospital, Saiseikai Niigata Daini Hospital, Saiseikai Suita Hospital, Saiseikai Matsuyama Hospital, Saiseikai Shigaken Hospital, Children's Hospital of Philadelphia, University of Pennsylvania, University of Illinois Chicago
Language: English
Subfield: Clinical Neurology
Field: Medicine
Domain: Health Sciences
Open Access status: green
Funder: National Cancer Institute
OpenAlex ID: W2789516721
