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Branchioma: immunohistochemical and molecular genetic study of 23 cases highlighting frequent loss of retinoblastoma 1 immunoexpression.
Bradová, Martina; Thompson, Lester D R; Hyrcza, Martin; Vanecek, Tomás; Grossman, Petr; Michal, Michael; Hájková, Veronika; Taheri, Touraj; Rupp, Niels; Suster, David; Lakhani, Sunil; Nikolov, Dimitar Hadzi; Zalud, Radim; Skálová, Alena; Michal, Michal; Agaimy, Abbas.
Afiliação
  • Bradová M; Department of Pathology, Faculty of Medicine in Pilsen, Charles University, E. Benese 13, 305 99, Pilsen, Czech Republic. bradova@biopticka.cz.
  • Thompson LDR; Bioptic Laboratory, Ltd, Pilsen, Czech Republic. bradova@biopticka.cz.
  • Hyrcza M; Head and Neck Pathology Consultations, Woodland Hills, CA, USA.
  • Vanecek T; Department of Pathology and Laboratory Medicine, University of Calgary, Calgary Laboratory Services, Foothills Medical Centre, Calgary, AB, Canada.
  • Grossman P; Molecular and Genetic Laboratory, Bioptic Laboratory, Ltd, Pilsen, Czech Republic.
  • Michal M; Molecular and Genetic Laboratory, Bioptic Laboratory, Ltd, Pilsen, Czech Republic.
  • Hájková V; Department of Pathology, Faculty of Medicine in Pilsen, Charles University, E. Benese 13, 305 99, Pilsen, Czech Republic.
  • Taheri T; Bioptic Laboratory, Ltd, Pilsen, Czech Republic.
  • Rupp N; Molecular and Genetic Laboratory, Bioptic Laboratory, Ltd, Pilsen, Czech Republic.
  • Suster D; School of Medicine and Pathology Queensland, University of Queensland, Brisbane, Australia.
  • Lakhani S; Department of Pathology and Molecular Pathology, University Hospital Zurich, Zurich, Switzerland.
  • Nikolov DH; Faculty of Medicine, University of Zurich, Zurich, Switzerland.
  • Zalud R; Department of Pathology, Rutgers University New Jersey Medical School, Newark, NJ, USA.
  • Skálová A; School of Medicine and Pathology Queensland, University of Queensland, UQCCR, Herston, Australia.
  • Michal M; Pathology Department, Regional Hospital Kolin, JSC, Kolin, Czech Republic.
  • Agaimy A; Pathology Department, Regional Hospital Kolin, JSC, Kolin, Czech Republic.
Virchows Arch ; 484(1): 103-117, 2024 Jan.
Article em En | MEDLINE | ID: mdl-37962685
ABSTRACT
Branchioma is an uncommon benign neoplasm with an adult male predominance, typically occurring in the lower neck region. Different names have been used for this entity in the past (ectopic hamartomatous thymoma, branchial anlage mixed tumor, thymic anlage tumor, biphenotypic branchioma), but currently, the term branchioma has been widely accepted. Branchioma is composed of endodermal and mesodermal lineage derivatives, in particular epithelial islands, spindle cells, and mature adipose tissue without preexistent thymic tissue or evidence of thymic differentiation. Twenty-three branchiomas were evaluated morphologically. Eighteen cases with sufficient tissue were assessed by immunohistochemistry, next-generation sequencing (NGS) using the Illumina Oncology TS500 panel, and fluorescence in situ hybridization (FISH) using an RB1 dual-color probe. All cases showed a biphasic morphology of epithelial and spindle cells with intermingled fatty tissue. Carcinoma arising in branchioma was detected in three cases. The neoplastic cells showed strong AE1/3 immunolabeling (100%), while the spindle cells expressed CD34, p63, and SMA (100%); AR was detected in 40-100% of nuclei (mean, 47%) in 14 cases. Rb1 showed nuclear loss in ≥ 95% of neoplastic cells in 16 cases (89%), while two cases revealed retained expression in 10-20% of tumor cell nuclei. NGS revealed a variable spectrum of likely pathogenic variants (n = 5) or variants of unknown clinical significance (n = 6). Loss of Rb1 was detected by FISH in two cases. Recent developments support branchioma as a true neoplasm, most likely derived from the rudimental embryological structures of endoderm and mesoderm. Frequent Rb1 loss by immunohistochemistry and heterozygous deletion by FISH is a real pitfall and potential confusion with other Rb1-deficient head and neck neoplasms (i.e., spindle cell lipoma), especially in small biopsy specimens.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Retinoblastoma / Neoplasias de Tecidos Moles / Timoma / Neoplasias do Timo / Branquioma / Neoplasias Epiteliais e Glandulares / Neoplasias da Retina Limite: Adult / Female / Humans / Male Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Retinoblastoma / Neoplasias de Tecidos Moles / Timoma / Neoplasias do Timo / Branquioma / Neoplasias Epiteliais e Glandulares / Neoplasias da Retina Limite: Adult / Female / Humans / Male Idioma: En Ano de publicação: 2024 Tipo de documento: Article