Browsing by Author "be59ddad-661f-4858-a1d8-d4eee3aa70a1"
Now showing items 1-6 of 6
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Quilodrán, Javier A.; Peña, Camila; Valladares, Ximena (Sociedad Medica de Santiago, 2017)© 2017, Sociedad Medica de Santiago. All rights reserved. Solitary extramedullary plasmacytomas represent 3% of plasma cell neoplasms. Their most common locations are the upper gastrointestinal and respiratory tract. We ...
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Erlij Opazo, Daniel; Cuellar, Carolina; Rivera, Angela; Badilla, Natalia; Moldenhauer, Nicia; Foster, Carolina; López, Bernardo; Valladares, Ximena; Stevens, Mary Ann (Sociedad Medica de Santiago, 2018)© 2018, Sociedad Medica de Santiago. All rights reserved. An assortment of clinical and laboratory abnormalities may occur as paraneoplastic syndromes in lymphomas. Rheumatological and dermatological manifestations such ...
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Erlij Opazo, Daniel; Cuellar, Carolina; Rivera, Angela; Badilla, Natalia; Moldenhauer, Nicia; Foster, Carolina; López, Bernardo; Valladares, Ximena; Stevens, Mary Ann (Sociedad Médica de Santiago, 2018-04)An assortment of clinical and laboratory abnormalities may occur as paraneoplastic syndromes in lymphomas. Rheumatological and dermatological manifestations such as paraneoplastic arthritis and pyoderma gangrenosum must ...
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Quilodrán, Javier A.; Peña, Camila; Valladares, Ximena (Sociedad Médica Santiago, 2017)Solitary extramedullary plasmacytomas represent 3% of plasma cell neoplasms. Their most common locations are the upper gastrointestinal and respiratory tract. We report a 70-year-old male presenting with progressive ...
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Erlij Opazo, Daniel; Calderón, Beatriz; Rivera, Angela; Mella, Cristián; Valladares, Ximena; Roessler, Emilio; Rivera, María Teresa; Méndez, Gonzalo (Ediciones Doyma, S.L., 2016)© 2015 Elsevier España, S.L.U. and Sociedad Española de Reumatología y Colegio Mexicano de ReumatologíaParaneoplastic syndromes can be presented in multiple ways, which include endocrinological, hematologic, rheumatologic ...
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Peña, Camila; Valladares, Ximena; Cabrera, María Elena (Sociedad Medica de Santiago, 2013)Secondary hemophagocytic syndrome (HFS) is an uncommon entity with a high mortality rate in adults, if no therapy is given. It is characterized by a severe hipercytokinemia due to a highly stimulated but ineffective immune ...