Sichelzellenanämie

School ager
with sickle cell disease and chest pain. CXR AP shows bibasilar infiltrates, right greater than left, and a small right pleural effusion.The diagnosis was acute chest syndrome.
pediatricimaging.org • CC-by-nc-sa 4.0
Teenager with
right upper quadrant pain and sickle cell disease. Sagittal (above) and transverse (below) US of the gallbladder show multiple small round echogenic mobile objects within the gallbladder that cause posterior shadowing.The diagnosis was cholelithiasis due to sickle cell disease.
pediatricimaging.org • CC-by-nc-sa 4.0
Teenager with
sickle cell disease and abdominal pain. AXR AP (left) shows faint calcifications in the right upper quadrant, just beneath the tip of the 12th rib and at the level of the L2 vertebral body which are better demonstrated on the coronal CT without contrast of the abdomen which demonstrates 5 calcifications within the gallbladder.The diagnosis was cholelithiasis in a patient with sickle cell disease.
pediatricimaging.org • CC-by-nc-sa 4.0
Computed
tomography of the spleen: how to interpret the hypodense lesion. Transverse contrast-enhanced CT images acquired during the portal venous phase. a A 43-year-old man with advanced sickle-cell disease. Note the irregular shape of the spleen, as well as the increased density of the splenic parenchyma, together with extensive calcifications as a consequence of constantly occurring micro-infarctions. b A 38-year-old man with sickle-cell disease exhibiting end-stage splenic involvement. Note the increased density, calcifications of the shrunken spleen
insightsimaging.springeropen.com • CC-by-2.0
Young adult
with back pain. Lateral radiograph of the thoracic spine shows multiple H-shaped vertebral bodies.The diagnosis was sickle cell disease.
pediatricimaging.org • CC-by-nc-sa 4.0
Radiopaedia • CC-by-nc-sa 3.0 • de

Sickle cell disease (SCD) (historically known as drepanocytosis) is a hereditary (autosomal recessive) condition resulting in the formation of abnormal hemoglobin (a hemoglobinopathy), which manifests as multisystem ischemia and infarction, as well as hemolytic anemia.

Hemoglobin SC (HbSC) disease, although a sickle cell disease subtype, with similarities to the classic condition, should ideally be considered as a distinct pathological entity .

Terminology

The term sickle cell disease is preferred to sickle cell anemia for the name of the condition, not least because the former term reflects the fact that the condition has multisystem effects, rather than just a severe form of anemia.

Epidemiology

There is no recognized gender predilection. The highest incidence occurs in individuals of African descent, followed by eastern Mediterranean and Middle Eastern populations. Malaria is the strongest known selective pressure on the human genome. The sickle cell mutation is prevalent in part as it confers a human genetic resistance to malaria as the abnormal hemoglobin has higher turnover and increased phagocytosis while sickled red cells have reduced cell-cell cytoadherence preventing the parasite from multiplying during the erythrocytic phase of its life cycle. It is estimated that approximately 8% of the African population is homozygous for sickle cell (where malaria is most prevalent).

Clinical presentation

The earliest manifestation is usually in early childhood, as babies are protected by elevated levels of fetal hemoglobin (HbF) in the first 6 months . The first presentation is commonly a painful vaso-occlusive crisis: sudden onset of bone or visceral pain due to microvascular occlusion and ischemia, often in the setting of sepsis or dehydration. Sickle cell disease is known to have a wide spectrum of clinical presentations from completely asymptomatic to a severe overwhelming crisis.

Clinical findings are wide and include :

Pathology

The disease results from a mutation in a gene coding for the beta chain of the hemoglobin molecule termed HbS. Specifically, there is a substitution of glutamine for valine at the 6th position in the beta-globin chain.

The term "sickle cell disease" applies to all patients who have two abnormal beta chains. The resultant hemoglobin molecules tend to clump together into long polymers, making the red blood cell (RBC) elongated (sickle-shaped), rigid and unable to deform appropriately when passing through small vessels, resulting in vascular occlusion. The abnormal RBCs are also removed from the bloodstream at an increased rate, leading to a hemolytic anemia .

Individuals with one HbS beta chain and one normal beta chain are said to have the "sickle cell trait". They are usually asymptomatic, although there is an association with an increased risk of renal medullary carcinoma . Perhaps of some consolation to individuals with the sickle cell trait is the increased resistance to malaria.

Individuals with one HbS beta chain and one hemoglobin C (HbC) beta chain, have a subtype of sickle cell disease known as hemoglobin SC (HbSC) disease .

Radiographic features

The radiographic manifestations of sickle cell disease are protean and are best discussed individually. Below is a summary of the main findings with links to individual articles.

Skeletal

Musculoskeletal manifestations of sickle cell disease are discussed separately. Three separate mechanisms can result in skeletal changes :

  • chronic anemia resulting in expansion of the medullary spaces
  • vaso-occlusive crises resulting in bone infarcts and subperiosteal hemorrhages
  • infection

    • These, in turn, can predispose individuals to other complications, such as growth disturbance and pathological fractures.

    Pulmonary

    Pulmonary involvement is a leading cause of mortality among sickle cell disease patients and can be acute or chronic:

    Abdominal

    Abdominal manifestations of sickle cell disease are discussed separately. Splenic infarction and subsequent functional asplenia tend to occur early in the disease.  The hepatobiliary and renal systems are also commonly involved.

    Cerebral

    Cerebral manifestations of sickle cell disease are discussed separately. Stroke and cerebral atrophy are common neurologic sequelae of sickle cell disease.

    Extramedullary hematopoiesis

    Extramedullary hematopoiesis is discussed separately. Less common in sickle cell disease than in other hemolytic anemias. The most common site is liver, followed by spleen, thorax, and adrenals .

    Treatment and prognosis

    Management of vaso-occlusive crises includes oxygen, hydration, and analgesia. Hydroxyurea decreases the severity of vaso-occlusive crises . Anemia is usually well-tolerated, however, blood transfusions may be indicated in some cases. Bone marrow transplantation may provide a cure.

    Sickle cell disease is associated with reduced life expectancy, whereas individuals with sickle cell trait have a normal life expectancy.

    See also

    Siehe auch:
    und weiter:
    Assoziationen und Differentialdiagnosen zu Sichelzellenanämie:
    extramedulläre
    Hämatopoese
    www.eurorad.org • CC by-nc-sa-4.0
    Milzinfarkt
     
    Wikipedia • CC BY-SA 4.0
    Thalassämie
     
    Wikipedia • CC BY-SA 4.0
    chronic lung
    disease
    pediatricimaging.org • CC-by-nc-sa 4.0
    medulläres
    Nierenkarzinom
    bmcnephrol.biomedcentral.com • CC-by-4.0
    Sichelzellenanämie
    (abdominelle Manifestationen)
    insightsimaging.springeropen.com • CC-by-2.0
    Acute chest
    syndrome bei Sichelzellanämie
    pediatricimaging.org • CC-by-nc-sa 4.0