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Low-grade adenosquamous carcinoma of the breast: a clinical, morphological and immunohistochemical analysis of 25 patients.
Lewis, Gloria; Fong, Nancy; Gjeorgjievski, Sandra Gjorgova; Li, Xiaoxian Bill; Li, Zaibo; Wei, Shi; Sturgis, Charles D; Wang, Chunjie; Komforti, Miglena; Zhang, Huina; Downs, Erinn; Cui, Xiaoyan; McIntire, Patrick; Hoda, Raza S; Rowe, J Jordi; Sciallis, Andrew; Zhang, Gloria.
Afiliación
  • Lewis G; Robert J. Tomsich Pathology and Laboratory Medicine Institute, Cleveland Clinic, Cleveland, OH, USA.
  • Fong N; Robert J. Tomsich Pathology and Laboratory Medicine Institute, Cleveland Clinic, Cleveland, OH, USA.
  • Gjeorgjievski SG; Department of Pathology and Laboratory Medicine, Emory University, Atlanta, GA, USA.
  • Li XB; Department of Pathology and Laboratory Medicine, Emory University, Atlanta, GA, USA.
  • Li Z; Department of Pathology and Laboratory Medicine, Ohio State University, Columbus, OH, USA.
  • Wei S; Department of Pathology and Laboratory Medicine, University of Kansas Medical Center, Kansas City, KS, USA.
  • Sturgis CD; Department of Pathology, University of Alabama at Birmingham, Birmingham, AL, USA.
  • Wang C; Department of Pathology and Laboratory Medicine, Mayo Clinic, Rochester, MN, USA.
  • Komforti M; Department of Pathology and Laboratory Medicine, University of Saskatchewan, Saskatoon, SK, Canada.
  • Zhang H; Department of Pathology and Laboratory Medicine, Mayo Clinic Florida, Jacksonville, FL, USA.
  • Downs E; Department of Pathology and Laboratory Medicine, University of Rochester, Rochester, NY, USA.
  • Cui X; Department of Pathology and Laboratory Medicine, Mayo Clinic Arizona, Scottsdale, AZ, USA.
  • McIntire P; Robert J. Tomsich Pathology and Laboratory Medicine Institute, Cleveland Clinic, Cleveland, OH, USA.
  • Hoda RS; Robert J. Tomsich Pathology and Laboratory Medicine Institute, Cleveland Clinic, Cleveland, OH, USA.
  • Rowe JJ; Robert J. Tomsich Pathology and Laboratory Medicine Institute, Cleveland Clinic, Cleveland, OH, USA.
  • Sciallis A; Robert J. Tomsich Pathology and Laboratory Medicine Institute, Cleveland Clinic, Cleveland, OH, USA.
  • Zhang G; Robert J. Tomsich Pathology and Laboratory Medicine Institute, Cleveland Clinic, Cleveland, OH, USA.
Histopathology ; 83(2): 252-263, 2023 Aug.
Article en En | MEDLINE | ID: mdl-37067767
AIMS: Due to its rarity and non-specific clinical and pathological features, low-grade adenosquamous carcinoma (LGASC) of the breast continues to pose diagnostic challenges. Unlike other triple-negative breast carcinomas, LGASC tends to have an indolent clinical behaviour. It is essential to recognise this lesion for accurate diagnosis and appropriate management. METHODS AND RESULTS: Twenty-five cases of LGASC were identified in our archives and collaborating institutes. Cases of LGASC with dominant coexisting other type carcinomas were excluded. We studied the clinical presentation, morphological features, patterns of the commonly used immunohistochemical stains and follow-up. In our cohort, LGASC was commonly located at the outer aspect of the breast and associated with intraductal papilloma. The morphology of LGASC is characterised by infiltrating small glands and nests with variable squamous differentiation. We also found cuffing desmoplastic (fibrolamellar) stromal change in 75% of patients and peripheral lymphocytic aggregates in 87.5% of patients. P63 and smooth muscle myosin (SMM) were the most common myoepithelial markers used to assist in diagnosis. P63 often stained peripheral tumour cells surrounding invasive glands (circumferential staining in 80% of the cases), mimicking myoepithelial cells. It also stained the small nests with squamous differentiation. However, SMM was negative in 63% of the cases. The vast majority of our cases were triple-negative; only a few had focal and weak expressions of ER and PR. One patient who did not have excision developed lymph node metastasis. Most patients underwent excision or mastectomy with negative margins as surgical treatment; there were no recurrences or metastases in these patients with clinical follow-ups up to 108 months. CONCLUSIONS: LGASC has some unique, although not entirely specific, morphological features and immunohistochemical staining patterns. Fibrolamellar stromal change, peripheral lymphocytic aggregates and variable staining of p63 and SMM are valuable features to facilitate the diagnosis.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Neoplasias de la Mama / Carcinoma de Células Escamosas / Carcinoma Adenoescamoso / Neoplasias de la Mama Triple Negativas Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Female / Humans Idioma: En Revista: Histopathology Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Neoplasias de la Mama / Carcinoma de Células Escamosas / Carcinoma Adenoescamoso / Neoplasias de la Mama Triple Negativas Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Female / Humans Idioma: En Revista: Histopathology Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos