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Titlebook: Diagnostic Pathology of Hematopoietic Disorders of Spleen and Liver; Ling Zhang,Haipeng Shao,Serhan Alkan Book 2020 Springer Nature Switze

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Thérèse M. F. Tuohy,Randall W. Burte other small B-cell lymphomas in the spleen show similar morphologic and phenotypic features of nodal/systemic diseases. The diagnosis of these small B-cell lymphomas is based on integration of clinical presentation, morphology, immunophenotype and genetic findings.
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History of Cancer Genetics in Man,dian age of 65, and has an indolent clinical course. Only 10% of patients died of disease complications, e.g., severe infection. The median survival of T-LGLL is more than 10 years. It was previously proposed that a sustained antigen stimulation leads to an altered apoptotic pathway of LGLs.
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History: Familial Adenomatous Polyposislymphoma/leukemia, unclassifiable as provisional entities according to the 2016 World Health Organization (WHO) classification. The clinicopathologic features of all rare lymphomas involving the spleen will be discussed in this chapter.
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Diagnostic Approaches to Hematopoietic Disorders of the Spleen and Liver, will focus on conventional diagnostic approaches to hematologic disorders of the liver and spleen, mainly including gross and microscopic examination and immunophenotyping. Biopsy indications and histology processes have also been discussed.   
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