Academic Journal

Fine-needle aspiration and effusion cytology of thoracic SMARCA4-deficient undifferentiated tumor and SMARCA4-deficient non-small cell lung carcinoma: A multi-institutional experience with 27 patients.

التفاصيل البيبلوغرافية
العنوان: Fine-needle aspiration and effusion cytology of thoracic SMARCA4-deficient undifferentiated tumor and SMARCA4-deficient non-small cell lung carcinoma: A multi-institutional experience with 27 patients.
المؤلفون: Zalles, Nicole, Mukhopadhyay, Sanjay, Satturwar, Swati, Lajara, Sigfred, Khader, Samer, Pantanowitz, Liron, Elsheikh, Tarik M
المصدر: Cancer Cytopathol ; ISSN:1934-6638 ; Volume:133 ; Issue:1
بيانات النشر: Wiley
سنة النشر: 2025
المجموعة: PubMed Central (PMC)
مصطلحات موضوعية: SMARCA4–deficient, cytology, effusion, fine‐needle aspiration, immunohistochemistry, non–small cell carcinoma, undifferentiated tumor
الوصف: Thoracic switch/sucrose nonfermentable-related, matrix-associated, actin-dependent regulator of chromatin, subfamily A, member 4 (SMARCA4)-deficient (SD) malignancies, including SD undifferentiated tumor (SD-UT) and SD non-small cell lung carcinoma (SD-NSCLC), have been recently described. The cytologic features of these neoplasms in fine-needle aspiration (FNA) and effusion specimens have rarely been reported in the literature. This study aimed to describe and compare the spectrum of cytologic, immunohistochemical, and clinical features of these high-grade malignancies recently encountered at the participating institutions.
نوع الوثيقة: article in journal/newspaper
report
اللغة: English
Relation: https://doi.org/10.1002/cncy.22919; https://pubmed.ncbi.nlm.nih.gov/39555952; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11695706/
DOI: 10.1002/cncy.22919
الاتاحة: https://doi.org/10.1002/cncy.22919
https://pubmed.ncbi.nlm.nih.gov/39555952
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11695706/
Rights: © 2024 The Author(s). Cancer Cytopathology published by Wiley Periodicals LLC on behalf of American Cancer Society.
رقم الانضمام: edsbas.695D6F23
قاعدة البيانات: BASE