Diagnóstico por imagem na avaliação da anemia falciforme

Yanaguizawa, Matiko; Taberner, Gustavo Sobreira; Cardoso, Fabiano Nassar; Natour, Jamil; Fernandes, Artur da Rocha Corrêa

doi:10.1590/s0482-50042008000200007

Cited by 8 publications

(9 citation statements)

References 10 publications

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“…This is another factor predisposing a patient to the presence of pain in this region. This osteonecrosis can occur in any bone, however it is more common in the humerus and femur 29,30 and is more prevalent in men and those with older age. Furthermore, the development of ulcers in the lower limbs, specifically the malleoli are common, causing severe pain and difficult scarring 31 .…”

Section: Discussionmentioning

confidence: 99%

Musculoskeletal pain, profile and quality of life of individuals with sickle cell disease

Ohara¹,

Ruas²,

Castro³

et al. 2012

Rev. bras. fisioter.

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Section: Discussionmentioning

confidence: 99%

Musculoskeletal pain, profile and quality of life of individuals with sickle cell disease

Ohara¹,

Ruas²,

Castro³

et al. 2012

Rev. bras. fisioter.

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“…Como casal com características falciformes, têm 25% de chance de ter um filho doente a cada gravidez, ou seja, SS homozigoto, com anemia falciforme, não sendo dominante em nenhum sexo (RAUBER, 2014). A avaliação dos pacientes pelo método da imagem está relacionado, especialmente, ao processo de diagnóstico e de companhamento das complicações que podem ocorrer ao decorrer ao longo da vida, sobretudo as que são de natureza vaso oclusiva (YANAGUIZAWA, 2008).…”

Section: Sequestro Do Sangue No Baçounclassified

Anemia Falciforme

Sousa

Fonseca

Miranda

et al. 2021

Rease

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A anemia falciforme (AF) é a doença sanguínea hereditária crônica mais comum no Brasil, com maior prevalência entre afrodescendentes. A AF origina-se de mutações no gene da β-globina, fazendo com que os glóbulos vermelhos apareçam em forma de foice quando perdem oxigênio em seu estado natural. Geralmente, se manifesta de maneira diferente em cada sujeito. Em alguns se apresenta com sintomas mais leves, e outros apresenta um ou mais sinais. Apresentando sintomas normalmente na segunda metade do primeiro ano de vida da criança. O objetivo deste trabalho é apresentar o diagnóstico laboratorial da anemia falciforme e dos seus portadores destes traços, ressaltando que esta enfermidade acomete todos os gêneros e raças. Este trabalho foi realizado por meio de uma revisão bibliográfica que buscou compreender todos elementos que envolvem o tema.

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“…SCD patients usually present common radiographic features due to lesions in the cortical bone and bone marrow, often affecting the maxillofacial area 30 . Maxillary bone alterations in SCD are classified as: (1) lesions with osteoporotic appearance due to bone marrow hyperplasia,…”

Section: Radiographic Alterationsmentioning

confidence: 99%

“…A less frequently radiographic finding is the expansion of bone marrow in the calvarium, which is more often observed in very young patients. The widening of the diploe narrows the outer table, while perpendicular orientation of trabeculae to inner table gives a "hair-on-end" or "bristlelike" appearance 30,31 . Radiopaque lesions presented by SCD patients are commonly associated to bone infarction and osteonecrosis [30][31] .…”

Section: Radiographic Alterationsmentioning

confidence: 99%

“…The widening of the diploe narrows the outer table, while perpendicular orientation of trabeculae to inner table gives a "hair-on-end" or "bristlelike" appearance 30,31 . Radiopaque lesions presented by SCD patients are commonly associated to bone infarction and osteonecrosis [30][31] . In the first situation, long bones are affected more often, yet osteonecrosis usually takes place in articular surfaces 38 .…”

Section: Radiographic Alterationsmentioning

confidence: 99%

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Prevalence of orofacial alterations in sickle cell disease: a review of literature

Santos¹,

Machado²,

Passos³

et al. 2013

Braz. J. Oral Sci.

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Aim: To evaluate the manifestations of sickle cell disease on the orofacial complex through a review of current literature concerning prevalence of dental caries, periodontal disease, temporomandibular joint disorders and radiographic alterations of maxillofacial bones. Methods: Full-text papers retrieved from MEDLINE and LILACS electronic databases were critically reviewed. Results: Alterations of maxillofacial bones are well documented in the literature, but studies reporting caries, periodontal condition and temporomandibular joint alterations in are scarce and inconclusive. Conclusion: Further well-designed epidemiological studies are needed to indicate the real impact of this disease on the stomatognathic health, collaborating to improve public health policies.

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Diagnóstico por imagem na avaliação da anemia falciforme

Cited by 8 publications

References 10 publications

Musculoskeletal pain, profile and quality of life of individuals with sickle cell disease

Musculoskeletal pain, profile and quality of life of individuals with sickle cell disease

Anemia Falciforme

Prevalence of orofacial alterations in sickle cell disease: a review of literature

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