Paraneoplastic vasculitis associated to pelvic chondrosarcoma: a case report

Vasculopathic syndromes have been associated with hematological and solid organ malignancies. The pathogenesis of these syndromes remains largely unknown and there are no biologic markers identified. Whether it is or is not a paraneoplastic syndrome is under discussion, the close temporal relationsh...

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Main Authors: Arvinius Camilla, González-Pérez Ana, García-Coiradas Javier, García-Maroto Roberto, Cebrián-Parra Juan Luis
Format: Article
Language:English
Published: EDP Sciences 2016-01-01
Series:SICOT-J
Subjects:
Online Access:http://dx.doi.org/10.1051/sicotj/2015042
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spelling doaj-873d3f51c3d244cb93509734d52671d22021-03-02T11:12:14ZengEDP SciencesSICOT-J2426-88872016-01-012810.1051/sicotj/2015042sicotj150159Paraneoplastic vasculitis associated to pelvic chondrosarcoma: a case reportArvinius CamillaGonzález-Pérez AnaGarcía-Coiradas JavierGarcía-Maroto RobertoCebrián-Parra Juan LuisVasculopathic syndromes have been associated with hematological and solid organ malignancies. The pathogenesis of these syndromes remains largely unknown and there are no biologic markers identified. Whether it is or is not a paraneoplastic syndrome is under discussion, the close temporal relationship of cancer and vasculitis suggests that these vasculitides are a paraneoplastic condition. We report a case of a 45-year-old female patient with pelvic chondrosarcoma who underwent surgical treatment and started to present visual loss, systemic inflammatory response syndrome (SRIS), cardiac insufficiency, hepatosplenomegaly, cholestasis as well as pulmonary bleeding suggesting a sarcoma-associated vasculitis. All antibodies were negative as in secondary vasculitis. After corticoideal therapy the vasculitis resolved and at 3-year follow-up the patient had not showed any further medical complications or recurrences of the vasculitis. The parallel evolution of the vasculitis and the solid tumor combined with the resolution of the vasculitis after corticotherapy enhances the likelihood of a paraneoplastic vasculitis associated with a chondrosarcoma according to literature review.http://dx.doi.org/10.1051/sicotj/2015042ChondrosarcomaVasculitisParaneoplasticSolid tumour
collection DOAJ
language English
format Article
sources DOAJ
author Arvinius Camilla
González-Pérez Ana
García-Coiradas Javier
García-Maroto Roberto
Cebrián-Parra Juan Luis
spellingShingle Arvinius Camilla
González-Pérez Ana
García-Coiradas Javier
García-Maroto Roberto
Cebrián-Parra Juan Luis
Paraneoplastic vasculitis associated to pelvic chondrosarcoma: a case report
SICOT-J
Chondrosarcoma
Vasculitis
Paraneoplastic
Solid tumour
author_facet Arvinius Camilla
González-Pérez Ana
García-Coiradas Javier
García-Maroto Roberto
Cebrián-Parra Juan Luis
author_sort Arvinius Camilla
title Paraneoplastic vasculitis associated to pelvic chondrosarcoma: a case report
title_short Paraneoplastic vasculitis associated to pelvic chondrosarcoma: a case report
title_full Paraneoplastic vasculitis associated to pelvic chondrosarcoma: a case report
title_fullStr Paraneoplastic vasculitis associated to pelvic chondrosarcoma: a case report
title_full_unstemmed Paraneoplastic vasculitis associated to pelvic chondrosarcoma: a case report
title_sort paraneoplastic vasculitis associated to pelvic chondrosarcoma: a case report
publisher EDP Sciences
series SICOT-J
issn 2426-8887
publishDate 2016-01-01
description Vasculopathic syndromes have been associated with hematological and solid organ malignancies. The pathogenesis of these syndromes remains largely unknown and there are no biologic markers identified. Whether it is or is not a paraneoplastic syndrome is under discussion, the close temporal relationship of cancer and vasculitis suggests that these vasculitides are a paraneoplastic condition. We report a case of a 45-year-old female patient with pelvic chondrosarcoma who underwent surgical treatment and started to present visual loss, systemic inflammatory response syndrome (SRIS), cardiac insufficiency, hepatosplenomegaly, cholestasis as well as pulmonary bleeding suggesting a sarcoma-associated vasculitis. All antibodies were negative as in secondary vasculitis. After corticoideal therapy the vasculitis resolved and at 3-year follow-up the patient had not showed any further medical complications or recurrences of the vasculitis. The parallel evolution of the vasculitis and the solid tumor combined with the resolution of the vasculitis after corticotherapy enhances the likelihood of a paraneoplastic vasculitis associated with a chondrosarcoma according to literature review.
topic Chondrosarcoma
Vasculitis
Paraneoplastic
Solid tumour
url http://dx.doi.org/10.1051/sicotj/2015042
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AT garciamarotoroberto paraneoplasticvasculitisassociatedtopelvicchondrosarcomaacasereport
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