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Malignant Blue Nevus
- Source :
- The American Journal of Dermatopathology. 25:21-27
- Publication Year :
- 2003
- Publisher :
- Ovid Technologies (Wolters Kluwer Health), 2003.
-
Abstract
- Malignant blue nevus is a rare melanocytic tumor that is described by some authors as a variant of malignant melanoma, whereas others regard it as a distinct entity. To our knowledge no molecular studies of this tumor have been performed, although the molecular pathogenesis of conventional melanomas has been extensively described. We present a case of malignant blue nevus that developed in a 15-cm congenital blue nevus on the back of a 41-year-old man. Subsequent regional lymph node and lung metastases developed within 1 and 29 months, respectively. We performed a molecular analysis for loss of heterozygosity on microdissected samples from the spectrum of benign to malignant blue nevus, using a panel of eight genes (MTS1, MXI1, CMM1, p53, NF1, L-myc hOGG1, and MCC), many of which are commonly associated with conventional melanomas. No loss of heterozygosity was detected, despite informativeness in seven genes. We suggest that malignant blue nevus may represent a distinct entity with a different molecular pathway to tumorigenesis than that of conventional melanomas.
- Subjects :
- Adult
Male
medicine.medical_specialty
Pathology
Lung Neoplasms
Skin Neoplasms
DNA Mutational Analysis
Loss of Heterozygosity
Dermatology
medicine.disease_cause
Polymerase Chain Reaction
Pathology and Forensic Medicine
Loss of heterozygosity
Nevus, Blue
Biomarkers, Tumor
medicine
Humans
Nevus
skin and connective tissue diseases
Blue nevus
Lymph node
DNA Primers
business.industry
Melanoma
DNA, Neoplasm
General Medicine
medicine.disease
Combined Modality Therapy
Malignant blue nevus
medicine.anatomical_structure
Histopathology
Lymph Nodes
medicine.symptom
business
Carcinogenesis
Subjects
Details
- ISSN :
- 01931091
- Volume :
- 25
- Database :
- OpenAIRE
- Journal :
- The American Journal of Dermatopathology
- Accession number :
- edsair.doi.dedup.....ee572e14b151343f989ec0ea413c293c
- Full Text :
- https://doi.org/10.1097/00000372-200302000-00005