Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Melanoma With Loss of BAP1 Expression in Patients With No Family History of BAP1-Associated Cancer Susceptibility Syndrome: A Case Series

28 Feb 2019

Abstract excerpt

The presence of multiple BAP1-negative melanocytic neoplasms is a hallmark of familial cancer susceptibility syndrome caused by germline mutations in BAP1. Melanocytic tumors lacking BAP1 expression may also present as sporadic lesions in patients lacking a germline BAP1 mutation. Here, we report histomorphologic and clinical characteristics of cutaneous melanomas with loss of BAP1 expression in 4 patients with...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Cutaneous Melanoma Detection and Management
Share to Integrated Circuits and Semiconductor Failure Analysis
Share to Occupational and environmental lung diseases

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 30801340
DOI: 10.1097/dad.0000000000001217

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Melanoma With Loss of BAP1 Expression in Patients With No Family History of BAP1-Associated Cancer Susceptibility Syndrome: A Case SeriesPMID 30801340Read ↗

Histomorphologic spectrum of BAP1 negative melanocytic neoplasms in a family with BAP1-associated cancer susceptibility syndrome.Semantic proximity Read ↗

Gene Expression and Mutational Profile in BAP-1 Inactivated Melanocytic Lesions of Progressive Malignancy from a Patient with Multiple Lesions.Semantic proximity Read ↗

Genotypic and Phenotypic Features of BAP1 Cancer Syndrome: A Report of 8 New Families and Review of Cases in the Literature.Semantic proximity Read ↗

Multiple Epithelioid Spitz Nevi or Tumors With Loss of BAP1 ExpressionSemantic proximity Read ↗

BAP1-Inactivated Melanoma Arising From BAP1-Inactivated Melanocytic Tumor in a Patient With BAP1 Germline Mutation: A Case Report and Review of the Literature.Semantic proximity Read ↗

BRCA1‐associated protein (BAP1)‐inactivated melanocytic tumorsSemantic proximity Read ↗

Tumours associated with BAP1 mutations.Semantic proximity Read ↗

Loss of BAP1 Expression in Basal Cell Carcinomas in Patients With Germline BAP1 Mutations.Semantic proximity Read ↗

A distinct subset of atypical Spitz tumors is characterized by BRAF mutation and loss of BAP1 expression.Semantic proximity Read ↗

Histomorphologic spectrum of germline-related and sporadic BAP1-inactivated melanocytic tumorsSemantic proximity Read ↗

BAP1 tumor predisposition syndrome case report: pathological and clinical aspects of BAP1-inactivated melanocytic tumors (BIMTs), including dermoscopy and confocal microscopy.Semantic proximity Read ↗

NRAS-mutated melanocytic BAP1-associated intradermal tumor (MBAIT): a case report.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.