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Author
- Dacic, Sanja2
- Nicholson, Andrew G2
- Aisner, Seena C1
- Attanoos, Richard L1
- Beasley, Mary Beth1
- Borczuk, Alain C1
- Botling, Johan1
- Brambilla, Elisabeth1
- Buettner, Reinhard H1
- Butnor, Kelly1
- Butnor, Kelly J1
- Chen, Gang1
- Chung, Jin-Haeng1
- Churg, Andrew1
- Cooper, Wendy1
- Duhig, Edwina1
- Flieder, Douglas B1
- Galateau-Salle, Francoise1
- Geisinger, Kim R1
- Hiroshima, Kenzo1
- Husain, Aliya N1
- Ishikawa, Yuichi1
- Kadota, Kyuichi1
- Keino, Naoto1
- Kerr, Keith1
Pathology Articles
2 Results
- Review Article
The 2021 WHO Classification of Tumors of the Pleura: Advances Since the 2015 Classification
Journal of Thoracic OncologyVol. 17Issue 5p608–622Published online: January 13, 2022- Jennifer L. Sauter
- Sanja Dacic
- Francoise Galateau-Salle
- Richard L. Attanoos
- Kelly J. Butnor
- Andrew Churg
- and others
Cited in Scopus: 15Substantial changes in the 2021 WHO Classification of Tumors of the Pleura and Pericardium since the 2015 WHO Classification include the following: (1) pleural and pericardial tumors have been combined in one chapter whereas in the 2015 WHO, pericardial tumors were classified with cardiac tumors; (2) well-differentiated papillary mesothelioma has been renamed well-differentiated papillary mesothelial tumor given growing evidence that these tumors exhibit relatively indolent behavior; (3) localized and diffuse mesothelioma no longer include the term “malignant” as a prefix; (4) mesothelioma in situ has been added to the 2021 classification because these lesions can now be recognized by loss of BAP1 and/or MTAP by immunohistochemistry and/or CDKN2A homozygous deletion by fluorescence in situ hybridization; (5) the three main histologic subtypes (i.e., epithelioid, biphasic, and sarcomatoid) remain the same but architectural patterns and cytologic and stromal features are more formally incorporated into the 2021 classification on the basis of their prognostic significance; (6) nuclear grading for epithelioid diffuse mesothelioma is introduced, and it is recommended to record this and other histologically prognostic features in pathology reports; (7) BAP1, EZH2, and MTAP immunohistochemistry have been found to be useful in separating benign mesothelial proliferations from mesothelioma; (8) biphasic mesothelioma can be diagnosed in small biopsies having both epithelioid and sarcomatoid components even if the amount of one component is less than 10%; and (9) the most frequently altered genes in diffuse pleural mesothelioma include BAP1, CDKN2A, NF2, TP53, SETD2, and SETDB1. - Original Article Small Cell Lung CancerOpen Archive
The Use of Immunohistochemistry Improves the Diagnosis of Small Cell Lung Cancer and Its Differential Diagnosis. An International Reproducibility Study in a Demanding Set of Cases
Journal of Thoracic OncologyVol. 12Issue 2p334–346Published online: December 17, 2016- Erik Thunnissen
- Alain C. Borczuk
- Douglas B. Flieder
- Birgit Witte
- Mary Beth Beasley
- Jin-Haeng Chung
- and others
Cited in Scopus: 82The current WHO classification of lung cancer states that a diagnosis of SCLC can be reliably made on routine histological and cytological grounds but immunohistochemistry (IHC) may be required, particularly (1) in cases in which histologic features are equivocal and (2) in cases in which the pathologist wants to increase confidence in diagnosis. However, reproducibility studies based on hematoxylin and eosin–stained slides alone for SCLC versus large cell neuroendocrine carcinoma (LCNEC) have shown pairwise κ scores ranging from 0.35 to 0.81.