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Clinical and dermoscopic features of cutaneous BAP1-inactivated melanocytic tumors: Results of a multicenter case-control study by the International Dermoscopy Society.
Yélamos, Oriol; Navarrete-Dechent, Cristián; Marchetti, Michael A; Rogers, Tova; Apalla, Zoe; Bahadoran, Philippe; Blázquez-Sánchez, Nuria; Busam, Klaus; Carrera, Cristina; Dusza, Stephen W; de la Fouchardière, Arnaud; Ferrara, Gerardo; Gerami, Pedram; Kittler, Harald; Lallas, Aimilios; Malvehy, Josep; Millán-Cayetano, José F; Nelson, Kelly C; Quan, Victor Li; Puig, Susana; Stevens, Howard; Thomas, Luc; Marghoob, Ashfaq A.
Afiliação
  • Yélamos O; Dermatology Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York; Dermatology Department, Hospital Clínic, Institut d'Investigacions Biomediques August Pi i Sunyer, Universitat de Barcelona, and CIBER de Enfermedades Raras, Instituto de Salud Carlos III, Barcel
  • Navarrete-Dechent C; Dermatology Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York; Department of Dermatology, Facultad de Medicina, Pontificia Universidad Católica de Chile, Santiago, Chile.
  • Marchetti MA; Dermatology Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.
  • Rogers T; Dermatology Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.
  • Apalla Z; First Department of Dermatology, Aristotle University, Thessaloniki, Greece.
  • Bahadoran P; Dermatology Department, Centre Hospitalier Universitaire de Nice, Nice, France.
  • Blázquez-Sánchez N; Dermatology Department, Hospital Costa del Sol, Marbella, Spain.
  • Busam K; Pathology Department, Memorial Sloan Kettering Cancer Center, New York, New York.
  • Carrera C; Dermatology Department, Hospital Clínic, Institut d'Investigacions Biomediques August Pi i Sunyer, Universitat de Barcelona, and CIBER de Enfermedades Raras, Instituto de Salud Carlos III, Barcelona, Spain.
  • Dusza SW; Dermatology Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.
  • de la Fouchardière A; Département de Biopathologie, Centre Léon Bérard, Lyon, France.
  • Ferrara G; Anatomic Pathology Unit, Hospital of Macerata, Macerata, Italy.
  • Gerami P; Dermatology Department, Feinberg School of Medicine, Northwestern University, Chicago, Illinois.
  • Kittler H; Department of Dermatology, Medical University of Vienna, Vienna, Austria.
  • Lallas A; First Department of Dermatology, Aristotle University, Thessaloniki, Greece.
  • Malvehy J; Dermatology Department, Hospital Clínic, Institut d'Investigacions Biomediques August Pi i Sunyer, Universitat de Barcelona, and CIBER de Enfermedades Raras, Instituto de Salud Carlos III, Barcelona, Spain.
  • Millán-Cayetano JF; Dermatology Department, Hospital Costa del Sol, Marbella, Spain.
  • Nelson KC; Dermatology Department, The University of Texas MD Anderson Cancer Center, Houston, Texas.
  • Quan VL; Dermatology Department, Feinberg School of Medicine, Northwestern University, Chicago, Illinois.
  • Puig S; Dermatology Department, Hospital Clínic, Institut d'Investigacions Biomediques August Pi i Sunyer, Universitat de Barcelona, and CIBER de Enfermedades Raras, Instituto de Salud Carlos III, Barcelona, Spain.
  • Stevens H; Skin Care Network, Barnet, London, United Kingdom.
  • Thomas L; Department of Dermatology, Lyon 1 University, Centre Hospitalier Lyon Sud and Lyon's Cancer Research Center INSERM U1052 - CNRS UMR5286, Lyon, France.
  • Marghoob AA; Dermatology Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.
J Am Acad Dermatol ; 80(6): 1585-1593, 2019 Jun.
Article em En | MEDLINE | ID: mdl-30244062
ABSTRACT

BACKGROUND:

Multiple BRCA1-associated protein 1 (BAP1)-inactivated melanocytic tumors (BIMTs) have been associated with a familial cancer syndrome involving germline mutations in BAP1.

OBJECTIVES:

We sought to describe the clinical and dermoscopic features of BIMTs.

METHODS:

This was a retrospective, multicenter, case-control study. Participating centers contributed clinical data, dermoscopic images, and histopathologic data of biopsy-proven BIMTs. We compared the dermoscopic features between BIMTs and control patients.

RESULTS:

The dataset consisted of 48 BIMTs from 31 patients (22 women; median age 37 years) and 80 control patients. Eleven patients had a BAP1 germline mutation. Clinically, most BIMTs presented as pink, dome-shaped papules (n = 24). Dermoscopically, we identified 5 patterns structureless pink-to-tan with irregular eccentric dots/globules (n = 14, 29.8%); structureless pink-to-tan with peripheral vessels (n = 10, 21.3%); structureless pink-to-tan (n = 7, 14.9%); a network with raised, structureless, pink-to-tan areas (n = 7, 14.9%); and globular pattern (n = 4, 8.5%). The structureless with eccentric dots/globules pattern and network with raised structureless areas pattern were only identified in BIMT and were more common in patients with BAP1 germline mutations (P < .0001 and P = .001, respectively).

LIMITATIONS:

Limitations included our small sample size, retrospective design, the absence of germline genetic testing in all patients, and inclusion bias toward more atypical-looking BIMTs.

CONCLUSIONS:

Dome-shaped papules with pink-to-tan structureless areas and peripheral irregular dots/globules or network should raise the clinical suspicion for BIMT.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Cutâneas / Proteínas Supressoras de Tumor / Ubiquitina Tiolesterase / Melanoma / Nevo Pigmentado Tipo de estudo: Observational_studies / Risk_factors_studies Limite: Adolescent / Adult / Aged / Child / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Cutâneas / Proteínas Supressoras de Tumor / Ubiquitina Tiolesterase / Melanoma / Nevo Pigmentado Tipo de estudo: Observational_studies / Risk_factors_studies Limite: Adolescent / Adult / Aged / Child / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2019 Tipo de documento: Article