12 research outputs found
Elementary Aspects of Constructive Commutative Algebra
hodes effectives et bornes de complexit'e. PhD thesis, ' Ecole Polytechnique, 1990. [60] F. Ollivier. Canonical bases: Relations with standard bases, finiteness conditions and application to tame automorphisms. In T. Mora and C. Traverso, editors, Effective Methods in Algebraic Geometry, volume 94 of Progress in Mathematics, pages 379--400. Birkhauser, 1991. From the Symposium MEGA 90, held at Castiglioncello, Italy, 1990. [61] F. Pauer and M. Pfeifhofer. The theory of Grobner bases. L'Enseignement Math'ematique, 34:215--232, 1988. [62] J.F. Pommaret. Differential Galois Theory. Gordon and Breach, 1983. [63] S. Rabinowitch. Zum Hilbertschen Nullstellensatz. Math. Ann., 102:520, 1929. [64] M. Reid. Undergraduate Algebraic Geometry, volume 12 of London Mathematical Society Student Texts. Cambridge University Press, 1988. [65] B. Renschuch. Elementare und Prakti
The fifth edition of the WHO classification of mature B-cell neoplasms: open questions for research.
The fifth edition of the World Health Organization Classification of Haematolymphoid Tumours (WHO-HAEM5) is the product of an evidence-based evolution of the revised fourth edition with wide multidisciplinary consultation. Nonetheless, while every classification incorporates scientific advances and aims to improve upon the prior version, medical knowledge remains incomplete and individual neoplasms may not be easily subclassified in a given scheme. Thus, optimal classification requires ongoing study, and there are certain aspects of some entities and subtypes that require further refinements. In this review, we highlight a selection of these challenging areas to prompt more research investigations. These include (1) a 'placeholder term' of splenic B-cell lymphoma/leukaemia with prominent nucleoli (SBLPN) to accommodate many of the splenic lymphomas previously classified as hairy cell leukaemia variant and B-prolymphocytic leukaemia, a clear new start to define their pathobiology; (2) how best to classify BCL2 rearrangement negative follicular lymphoma including those with BCL6 rearrangement, integrating the emerging new knowledge on various germinal centre B-cell subsets; (3) what is the spectrum of non-IG gene partners of MYC translocation in diffuse large B-cell lymphoma/high-grade B-cell lymphoma and how they impact MYC expression and clinical outcome; how best to investigate this in a routine clinical setting; and (4) how best to define high-grade B-cell lymphoma not otherwise specified and high-grade B-cell lymphoma with 11q aberrations to distinguish them from their mimics and characterise their molecular pathogenetic mechanism. Addressing these questions would provide more robust evidence to better define these entities/subtypes, improve their diagnosis and/or prognostic stratification, leading to better patient care. © 2024 The Authors. The Journal of Pathology published by John Wiley & Sons Ltd on behalf of The Pathological Society of Great Britain and Ireland
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The fifth edition of the WHO classification of mature Bâcell neoplasms: open questions for research
Publication status: PublishedThe fifth edition of the World Health Organization Classification of Haematolymphoid Tumours (WHOâHAEM5) is the product of an evidenceâbased evolution of the revised fourth edition with wide multidisciplinary consultation. Nonetheless, while every classification incorporates scientific advances and aims to improve upon the prior version, medical knowledge remains incomplete and individual neoplasms may not be easily subclassified in a given scheme. Thus, optimal classification requires ongoing study, and there are certain aspects of some entities and subtypes that require further refinements. In this review, we highlight a selection of these challenging areas to prompt more research investigations. These include (1) a âplaceholder termâ of splenic Bâcell lymphoma/leukaemia with prominent nucleoli (SBLPN) to accommodate many of the splenic lymphomas previously classified as hairy cell leukaemia variant and Bâprolymphocytic leukaemia, a clear new start to define their pathobiology; (2) how best to classify BCL2 rearrangement negative follicular lymphoma including those with BCL6 rearrangement, integrating the emerging new knowledge on various germinal centre Bâcell subsets; (3) what is the spectrum of nonâIG gene partners of MYC translocation in diffuse large Bâcell lymphoma/highâgrade Bâcell lymphoma and how they impact MYC expression and clinical outcome; how best to investigate this in a routine clinical setting; and (4) how best to define highâgrade Bâcell lymphoma not otherwise specified and highâgrade Bâcell lymphoma with 11q aberrations to distinguish them from their mimics and characterise their molecular pathogenetic mechanism. Addressing these questions would provide more robust evidence to better define these entities/subtypes, improve their diagnosis and/or prognostic stratification, leading to better patient care. © 2024 The Authors. The Journal of Pathology published by John Wiley & Sons Ltd on behalf of The Pathological Society of Great Britain and Ireland