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Paravertebral pseudotumor in patient with hereditary spherocytosis

As a rare complication in chronic anemic states, the extramedullary hematopoiesis may provide diagnostic and therapeutic challenge. Caused by the insufficiency of the bone marrow with reactivation of quiescent erythropoietic sites, this condition may vary its presentation as a simple radiologic find...

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Autores principales: Rabelo, Lêda Maria, Vieira, Vítor Lopes Galvão, dos Santos, Gustavo Rengel, Heimbecker, Giselle, Escuissato, Dante Luiz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4976615/
https://www.ncbi.nlm.nih.gov/pubmed/27536548
http://dx.doi.org/10.1016/j.rmcr.2016.07.011
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author Rabelo, Lêda Maria
Vieira, Vítor Lopes Galvão
dos Santos, Gustavo Rengel
Heimbecker, Giselle
Escuissato, Dante Luiz
author_facet Rabelo, Lêda Maria
Vieira, Vítor Lopes Galvão
dos Santos, Gustavo Rengel
Heimbecker, Giselle
Escuissato, Dante Luiz
author_sort Rabelo, Lêda Maria
collection PubMed
description As a rare complication in chronic anemic states, the extramedullary hematopoiesis may provide diagnostic and therapeutic challenge. Caused by the insufficiency of the bone marrow with reactivation of quiescent erythropoietic sites, this condition may vary its presentation as a simple radiologic finding to a spontaneous massive haemothorax. In this paper, we report the case of a 61-years-old female patient with hereditary spherocitosys and paravertebral masses, focusing on clinical and radiological findings in CT and MRI to conclude the tumors etiology and provide adequate care.
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spelling pubmed-49766152016-08-17 Paravertebral pseudotumor in patient with hereditary spherocytosis Rabelo, Lêda Maria Vieira, Vítor Lopes Galvão dos Santos, Gustavo Rengel Heimbecker, Giselle Escuissato, Dante Luiz Respir Med Case Rep Case Report As a rare complication in chronic anemic states, the extramedullary hematopoiesis may provide diagnostic and therapeutic challenge. Caused by the insufficiency of the bone marrow with reactivation of quiescent erythropoietic sites, this condition may vary its presentation as a simple radiologic finding to a spontaneous massive haemothorax. In this paper, we report the case of a 61-years-old female patient with hereditary spherocitosys and paravertebral masses, focusing on clinical and radiological findings in CT and MRI to conclude the tumors etiology and provide adequate care. Elsevier 2016-07-27 /pmc/articles/PMC4976615/ /pubmed/27536548 http://dx.doi.org/10.1016/j.rmcr.2016.07.011 Text en © 2016 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Case Report
Rabelo, Lêda Maria
Vieira, Vítor Lopes Galvão
dos Santos, Gustavo Rengel
Heimbecker, Giselle
Escuissato, Dante Luiz
Paravertebral pseudotumor in patient with hereditary spherocytosis
title Paravertebral pseudotumor in patient with hereditary spherocytosis
title_full Paravertebral pseudotumor in patient with hereditary spherocytosis
title_fullStr Paravertebral pseudotumor in patient with hereditary spherocytosis
title_full_unstemmed Paravertebral pseudotumor in patient with hereditary spherocytosis
title_short Paravertebral pseudotumor in patient with hereditary spherocytosis
title_sort paravertebral pseudotumor in patient with hereditary spherocytosis
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4976615/
https://www.ncbi.nlm.nih.gov/pubmed/27536548
http://dx.doi.org/10.1016/j.rmcr.2016.07.011
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