The xanthogranulomatous process (XP), is a form of acute and chronic inflammation characterized by an exuberant clustering of foamy macrophages among other inflammatory cells. Localization in the kidney and renal pelvis has been the most frequent and better known occurrence followed by that in the gallbladder but many others have been subsequently recorded.[1][2][3] The pathological findings of the process and etiopathogenetic and clinical observations have been reviewed by Cozzutto and Carbone.[4]
^Goodman M, Curry T, Russell T (March 1979). "Xanthogranulomatous pyelonephritis (XGP): a local disease with systemic manifestations. Report of 23 patients and review of the literature". Medicine (Baltimore). 58 (2): 171–81. doi:10.1097/00005792-197903000-00005. PMID 431402. S2CID 30142314.
^Goodman ZD, Ishak KG (October 1981). "Xanthogranulomatous cholecystitis". Am. J. Surg. Pathol. 5 (7): 653–9. doi:10.1097/00000478-198110000-00007. PMID 7337158. S2CID 22921484.
^Franco V, Aragona F, Genova G, Florena AM, Stella M, Campesi G (June 1990). "Xanthogranulomatous cholecystitis. Histopathological study and classification". Pathol. Res. Pract. 186 (3): 383–90. doi:10.1016/S0344-0338(11)80297-9. PMID 2377572.
^Cozzutto C, Carbone A (August 1988). "The xanthogranulomatous process. Xanthogranulomatous inflammation". Pathol. Res. Pract. 183 (4): 395–402. doi:10.1016/S0344-0338(88)80085-2. PMID 3054826.
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