Abstract
The first known description of spontaneous splenic rupture was by Rokitansky, who described the spontaneous rupture of a leukemic spleen in 1861.1 This condition, known as spontaneous splenic rupture, has been described most commonly as occurring in patients with infectious diseases, e.g., malaria and infectious mononucleosis. It has also been described as occurring with many other disease states, however, including endocarditis, typhoid fever, tuberculosis, influenza, and sarcoidosis,2 as well as in amyloidosis and normal spleens.3 As you will see, spontaneous splenic rupture is also well described in many malignant disease processes.
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© 1987 Springer Science+Business Media New York
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Goldstone, S.E., Gold, M.S. (1987). Spontaneous Splenic Rupture. In: Dutcher, J.P., Wiernik, P.H. (eds) Handbook of Hematologic and Oncologic Emergencies. Springer, Boston, MA. https://doi.org/10.1007/978-1-4899-0476-8_20
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DOI: https://doi.org/10.1007/978-1-4899-0476-8_20
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