Galería de imágenes
Incidental detection of Borrelia recurrentis (->) in a patient initially suspected to suffer from malaria. Borrelia recurrentis is transmitted by lice and ticks and is the causative agent of relapsing fever. Like malaria, relapsing fever often is a travel-related disease that, after an incubation time of up to 2 weeks, leads to fever attacks.
<p>Incidental detection of Borrelia recurrentis (->) in a patient initially suspected to suffer from malaria. Borrelia recurrentis is transmitted by lice and ticks and is the causative agent of relapsing fever. Like malaria, relapsing fever often is a travel-related disease that, after an incubation time of up to 2 weeks, leads to fever attacks.</p>
In the peripheral blood (May-Grünwald-Giemsa stain) of this 75-year old woman with PV all three cell lineages are increased: haemoglobin concentration 16 g/dL, white blood cell count 15,000/µL, platelet count 980,000/µL. In functional iron deficiency red blood cells often are microcytic. The MCV is only 75 fL. The haematopoietic cells of the patient show a JAK2 mutation.
<p>In the peripheral blood (May-Grünwald-Giemsa stain) of this 75-year old woman with PV all three cell lineages are increased: haemoglobin concentration 16 g/dL, white blood cell count 15,000/µL, platelet count 980,000/µL. In functional iron deficiency red blood cells often are microcytic. The MCV is only 75 fL. The haematopoietic cells of the patient show a JAK2 mutation.</p>
Infectious mononucleosis is an acute condition caused by the Epstein-Barr virus (EBV). The disease is highly contagious and spreads via body secretions, especially saliva. The infection frequently goes unnoticed in children; however, mainly adolescents and young adults exhibit symptoms. Infected B lymphocytes induce a humoral (B cell) as well as a cellular (T cell) immune response which can be seen in an increased concentration of atypical lymphocytes in the blood film.
<p>Infectious mononucleosis is an acute condition caused by the Epstein-Barr virus (EBV). The disease is highly contagious and spreads via body secretions, especially saliva. The infection frequently goes unnoticed in children; however, mainly adolescents and young adults exhibit symptoms. Infected B lymphocytes induce a humoral (B cell) as well as a cellular (T cell) immune response which can be seen in an increased concentration of atypical lymphocytes in the blood film. </p>
Bone marrow histology (haematoxylin eosin stain) of a patient with breast cancer showing an infiltration of the bone marrow by a lobular carcinoma of the breast.
<p>Bone marrow histology (haematoxylin eosin stain) of a patient with breast cancer showing an infiltration of the bone marrow by a lobular carcinoma of the breast.</p>
Bone marrow histology of a patient with breast cancer showing an infiltration of the bone marrow by a lobular carcinoma of the breast. The increased number of fibres is coloured black after Gomori staining.
<p>Bone marrow histology of a patient with breast cancer showing an infiltration of the bone marrow by a lobular carcinoma of the breast. The increased number of fibres is coloured black after Gomori staining.</p>
Due to an increased production of red blood cells in PV iron in the bone marrow gets 'used up', causing functional iron deficiency in the bone marrow. The detection of iron accumulation (->) in the bone marrow by Prussian Blue stain, as shown here, argues against PV.
<p>Due to an increased production of red blood cells in PV iron in the bone marrow gets 'used up', causing functional iron deficiency in the bone marrow. The detection of iron accumulation (->) in the bone marrow by Prussian Blue stain, as shown here, argues against PV.</p>
Patient with established severe iron deficiency anaemia (haemoglobin 5 g/dL). Well recognisable are anulocytes (->) and unusually small red blood cells – compared to a normal lymphocyte. The MCV was 53 fL.
<p>Patient with established severe iron deficiency anaemia (haemoglobin 5 g/dL). Well recognisable are anulocytes (->) and unusually small red blood cells – compared to a normal lymphocyte. The MCV was 53 fL.</p>
Peripheral blood (May-Grünwald-Giemsa stain) of a patient with isolated congenital reduction of erythropoiesis in the bone marrow (pure red cell aplasia, PRCA). The haemoglobin concentration was 9.2 g/dL, white blood cell and platelet counts were normal.
<p>Peripheral blood (May-Grünwald-Giemsa stain) of a patient with isolated congenital reduction of erythropoiesis in the bone marrow (pure red cell aplasia, PRCA). The haemoglobin concentration was 9.2 g/dL, white blood cell and platelet counts were normal.</p>
Leucoerythroblastic condition and schistocytes in a patient with colorectal carcinoma. The occurrence of schistocytes (->) in tumour patients is sometimes an indication of tumour infiltration of the bone marrow.
<p>Leucoerythroblastic condition and schistocytes in a patient with colorectal carcinoma. The occurrence of schistocytes (->) in tumour patients is sometimes an indication of tumour infiltration of the bone marrow.</p>