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An adolescent with hereditary spherocytosis who presented with splenic infarction
A 16-year-old male patient with known hereditary spherocytosis presented with a 4-day history of chest pain and lethargy. On admission, he had a low-grade fever and was grossly anaemic; examination revealed splenomegaly. An ultrasound scan confirmed splenomegaly with areas of splenic infarction. Sub...
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| Publicado no: | BMJ Case Rep |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BMJ Publishing Group
2015
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4493230/ https://ncbi.nlm.nih.gov/pubmed/26139647 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bcr-2014-206196 |
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