Hyperchromasia (or hyperchromasia) is a condition of body tissues in which they become brighter and more saturated colors. This can be caused by a variety of factors, such as changes in hormone levels, immune system problems, and other medical conditions.
One of the most well-known cases of hyperchromia is Cushing's syndrome, which is associated with increased production of adrenocorticotropic hormone (ACTH). In this condition, the body produces too much cortisol (the stress hormone), which leads to increased production of the skin pigment melanin and increased skin brightness.
Hyperchromia can also occur in people suffering from autoimmune diseases such as Hashimoto's thyroiditis and lupus. In these cases, the body begins to react to its own tissues and cells, which can lead to increased melanin production and changes in skin color. In addition, hyperchromasia can occur in some malignancies, including skin, breast, and lung cancers.
Treatment of hyperchrosia depends on the cause of its occurrence. For example, autoimmune diseases may require medications to suppress the immune system. If the cause is a benign tumor, surgical removal or radiation may be possible to reduce the size of the tumor.
CHROMASIA (Greek hyper- change, transition through, change + chroma dye; synonym: hyperchromia, nonaplasia) changes in the color of cells in the urine, altered erythrocytes and leukocytes under a microscope, observed during transfusion of incompatible blood. A distinction is made between the rare pathological and the more frequently observed physiological. The latter occurs due to unusual coloring
Hyperchromism (hyperchromatism) is a syndrome characterized by an increase in the level of hemoglobin in the blood and an increase in the total amount of colored hemoglobin pigment (hemoglobin crystal hydration).
Hyperchromic elements, which, due to their larger size, contain fewer hemoglobin molecules in a smaller area, adsorb light better, and as a result,