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- Mohamed E. Salama
- 1Department of Pathology, Stanford University School of Medicine, Stanford, CA
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- Izidore S. Lossos
- 2Department of Medicine, Division of Hematology-Oncology and Molecular and Cellular Pharmacology, Sylvester Comprehensive Cancer Center, University of Miami, Miami, FL
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- Roger A. Warnke
- 1Department of Pathology, Stanford University School of Medicine, Stanford, CA
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- Yasodha Natkunam
- 1Department of Pathology, Stanford University School of Medicine, Stanford, CA
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説明
<jats:title>Abstract</jats:title> <jats:p>Nodal marginal zone lymphoma (NMZL) represents a rare and heterogeneous group that lacks markers specific for the diagnosis. We evaluated morphologic and immunoarchitectural features of 51 NMZLs, and the following immunostains were performed: CD20, CD21, CD23, CD5, CD3, CD43, CD10, Ki-67, BCL1, BCL2, BCL6, HGAL, and LMO2. Four immunoarchitectural patterns were evident: diffuse (38 [75%]), well-formed nodular/follicular (5 [10%]), interfollicular (7 [14%]), and perifollicular (1 [2%]). Additional features included a monocytoid component (36 [71%]), admixed large cells (20 [39%]), plasma cells (24 [47%]), compartmentalizing stromal sclerosis (13 [25%]), and prominent blood vessel sclerosis (10 [20%]). CD21 highlighted disrupted follicular dendritic cell meshwork in 35 (71%) of 49 cases, and CD43 coexpression was present in 10 (24%) of 42 cases. A panel of germinal center–associated markers was helpful in eliminating cases of diffuse follicle center lymphoma. Our results highlight the histologic and immunoarchitectural spectrum of NMZL and the usefulness of immunohistochemical analysis for CD43, CD23, CD21, BCL6, HGAL, and LMO2 in the diagnosis of NMZL.</jats:p>
収録刊行物
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- American Journal of Clinical Pathology
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American Journal of Clinical Pathology 132 (1), 39-49, 2009-07-01
Oxford University Press (OUP)