Pulmonary hypertension in Langerhans cell histiocytosis (Q104904): Difference between revisions
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Aumento da pressão arterial em artéria pulmonar, veia pulmonar ou capilares pulmonares, conjuntamente conhecidos como vasculatura pulmonar, levando a falta de ar, tonturas, desmaios e outros sintomas, todos estes exacerbados pelo esforço, na histiocitose celular de Langerhan. | |||
| description / en | description / en | ||
This is an increase of blood pressure in the pulmonary artery, pulmonary vein, or pulmonary capillaries, together known as the lung vasculature, leading to shortness of breath, dizziness, fainting, and other symptoms, all of which are exacerbated by exertion, in Langerhans cell histiocytosis. | |||
Revision as of 10:46, 17 August 2026
This is an increase of blood pressure in the pulmonary artery, pulmonary vein, or pulmonary capillaries, together known as the lung vasculature, leading to shortness of breath, dizziness, fainting, and other symptoms, all of which are exacerbated by exertion, in Langerhans cell histiocytosis.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1936212382 |
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| English | Pulmonary hypertension in Langerhans cell histiocytosis |
This is an increase of blood pressure in the pulmonary artery, pulmonary vein, or pulmonary capillaries, together known as the lung vasculature, leading to shortness of breath, dizziness, fainting, and other symptoms, all of which are exacerbated by exertion, in Langerhans cell histiocytosis. |
