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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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Detalles Bibliográficos
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
Descripción
Sumario: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.