Abstract
A broad range of reactive and systemic disorders may be manifest in the spleen. Trauma and physical damage to the spleen are discussed, as well as their histologic appearances. Perisplenitis, or sugar-coated spleen, is illustrated. Fibrocongestive splenomegaly, a final common pathway of chronic vascular compromise, is shown. The splenic effects of red blood cell disorders, including thalassemia, sickle cell disease, and hereditary spherocytosis, are illustrated. Granulomas of a variety of causes are shown. The splenic manifestations of the rare histiocyte-derived disorder, Langerhans cell histiocytosis, is shown. A variety of unusual disorders, including Castleman disease, and effects of various therapies are illustrated. A broad range of autoimmune disorders will have significant findings in the spleen and these are discussed. Finally, this chapter shows a range of congenital immunodeficiency disorders that involve the spleen.
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Reference
O’Malley DP, George TI, Orazi A, Abbondanzo S. Armed Forces Institute of Pathology: Benign and reactive conditions of lymph node and spleen [book]. Silver Spring, MD: American Registry of Pathology Press; 2009.
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© 2013 Springer Science+Business Media New York
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O’Malley, D.P. (2013). Reactive and Systemic Conditions. In: Atlas of Spleen Pathology. Atlas of Anatomic Pathology. Springer, New York, NY. https://doi.org/10.1007/978-1-4614-4672-9_6
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DOI: https://doi.org/10.1007/978-1-4614-4672-9_6
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Publisher Name: Springer, New York, NY
Print ISBN: 978-1-4614-4671-2
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