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Microsecretory adenocarcinoma of the skin harboring recurrent SS18 fusions: A cutaneous analog to a newly described salivary gland tumor.
Bishop, Justin A; Williams, Erik A; McLean, Anne C; Gagan, Jeffrey; Rooper, Lisa M; Jordan, Richard C K; LeBoit, Philip E.
Afiliação
  • Bishop JA; Department of Pathology, UT Southwestern Medical Center, Dallas, Texas, USA.
  • Williams EA; UCSF Dermatopathology & Oral Pathology Service, Department of Pathology and Dermatology, University of California, San Francisco, California, USA.
  • McLean AC; Department of Pathology, UT Southwestern Medical Center, Dallas, Texas, USA.
  • Gagan J; Department of Pathology, UT Southwestern Medical Center, Dallas, Texas, USA.
  • Rooper LM; Department of Pathology, The Johns Hopkins Hospital, Baltimore, Maryland, USA.
  • Jordan RCK; UCSF Dermatopathology & Oral Pathology Service, Department of Pathology and Dermatology, University of California, San Francisco, California, USA.
  • LeBoit PE; UCSF Dermatopathology & Oral Pathology Service, Department of Pathology and Dermatology, University of California, San Francisco, California, USA.
J Cutan Pathol ; 50(2): 134-139, 2023 Feb.
Article em En | MEDLINE | ID: mdl-35690998
ABSTRACT

BACKGROUND:

Microsecretory adenocarcinoma (MSA) is a newly described salivary gland neoplasm characterized by MEF2CSS18 fusions. MSA was previously thought to occur exclusively in salivary glands. Here, we expand the spectrum of known primary sites of this tumor by describing a series of cutaneous tumors with analogous findings.

METHODS:

We identified four cutaneous primary tumors with histopathologic features identical to MSA of the salivary glands. These cases were evaluated by immunohistochemistry, fluorescence in situ hybridization (FISH) for SS18 rearrangement and targeted RNA-sequencing. We also queried a pan-tumor database of advanced carcinomas for MEF2CSS18.

RESULTS:

The cases occurred in men ranging from 61 to 74 years (mean, 68). They arose from the skin of the nose, chin, scalp, and external auditory canal. All included cords/microcysts of eosinophilic cells with bland oval nuclei and bluish mucin within fibromyxoid stroma. The scalp tumor also exhibited high-grade transformation (marked atypia, elevated mitotic rate, and necrosis), a feature unreported in salivary MSA. By immunohistochemistry, all cases were positive for S100. Two showed a myoepithelial component positive for p40 and smooth muscle actin or calponin. Three cases harbored MEF2CSS18 by RNA sequencing, while one with limited tissue had SS18 rearrangement via FISH. Two patients had no evidence of recurrence or metastasis in limited follow-up (3 and 6 months). The pan-tumor database query also did not identify MEF2CSS18 in any advanced cutaneous carcinomas.

CONCLUSION:

This report expands the sites that can be involved by MSA. Similar to salivary cases, MEF2CSS18 represents a recurrent fusion in MSA of the skin. Unusual features in cutaneous cases not seen in salivary MSA include one case with high-grade transformation and two cases with a myoepithelial cell component. Identification of this fusion expands the spectrum of salivary-analog cutaneous tumors and aids in precise tumor classification.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Cutâneas / Neoplasias das Glândulas Salivares / Carcinoma / Adenocarcinoma Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: J Cutan Pathol Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Cutâneas / Neoplasias das Glândulas Salivares / Carcinoma / Adenocarcinoma Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: J Cutan Pathol Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Estados Unidos