These other conditions may occur separately or together with haemosiderosis.

Other definitions distinguishing haemochromatosis or haemosiderosis that are occasionally used include:

There are many pulmonary problems that may seem to mimic haemosiderosis but do not necessarily include the deposits of iron into the lung.

This treatment should not be maintained for longer periods because of the risks of haemosiderosis, red cell sensitisation and infection associated with transfusion.

Hemosiderosis (AmE) or haemosiderosis (BrE) is a form of iron overload disorder resulting in the accumulation of hemosiderin.

In general, the term haemosiderosis is used to indicate the pathological effect of iron accumulation in any given organ, which mainly occurs in the form of haemosiderin.

Idiopathic pulmonary haemosiderosis can occur either as a primary lung disorder or as the sequela to other pulmonary, cardiovascular or immune system disorder.

Haemosiderosis is haemochromatosis caused by excessive blood transfusions, that is, haemosiderosis is a form of secondary haemochromatosis.

Idiopathic pulmonary haemosiderosis (or idiopathic pulmonary hemosiderosis; IPH) is a lung disease of unknown cause that is characterized by alveolar capillary bleeding and accumulation of haemosiderin in the lungs.

In addition under microscopy, chronic diffuse typhlitis, haemosiderosis, granulomas with necrotic center in the submucosa and leiomyomas in the submucosa, muscular and serosa associated with immature H. gallinarum worms were observed.

Kubba and Young have pointed out a number of other conceivable, if unlikely, diagnoses, besides cystic fibrosis and alfa 1-antitripsin deficiency: Churg-Strauss syndrome, allergic bronchopulmonary aspergillosis, hypogammaglobulinemia, idiopathic pulmonary haemosiderosis, lung abscesses, and pulmonary arteriovenous malformations.

There are several methods available for diagnosing and monitoring hemosiderosis including:

The lung disease commonly causes bleeding into the lungs and results in pulmonary hemosiderosis.

A long-standing hyphema may result in hemosiderosis and heterochromia.

Atransferrinemia is characterized by anemia and hemosiderosis in the heart and liver.

Mitral stenosis can also lead to pulmonary hemosiderosis.

Ferritin is also used as a marker for iron overload disorders, such as hemochromatosis or hemosiderosis.

Relatively few extravasated red cells are lysed so the resulting hemosiderosis is limited and results in a progressively more pale area of infarction with time.

Before using this medication, consult your doctor or pharmacist if you have: iron overload disorder (e.g., hemochromatosis, hemosiderosis).

Iron chelation by deferoxamine in sickle cell patients with severe transfusion-induced hemosiderosis: a randomized, double-blind study of the dose-response relationship.

Superficial hemosiderosis of the central nervous system is a disease of the brain resulting from chronic iron deposition in neuronal tissues associated with cerebrospinal fluid.

These lesions within these organs are characterized by well-circumscribed focal fibrosis, accumulation of eosinophils and histiocytes, hemorrhage or hemosiderosis with the loss of normal architecture.

Hemosiderin deposition in the lungs is often seen after diffuse alveolar hemorrhage, which occurs in diseases such as Goodpasture's syndrome, Wegener's granulomatosis, and idiopathic pulmonary hemosiderosis.

Although lemurs in captivity have been shown to be prone to hemosiderosis, the frequency of the disease varies across institutions and may depend on the diet, husbandry protocols, and genetic stock.

An absence of transferrin results from a rare genetic disorder known as atransferrinemia; a condition characterized by anemia and hemosiderosis in the heart and liver that leads to many complications, including heart failure.

Jan Waldenström (1906-1996) was a renowned clinician and researcher whose observations in hematology provided frameworks for understanding diseases such as porphyria, hemosiderosis and what is now known as Waldenström's macroglobulinemi.

Other names for this syndrome include Finnish lethal neonatal metabolic syndrome (FLNMS); lactic acidosis, Finnish, with hepatic hemosiderosis; and Fellman syndrome.

Idiopathic pulmonary haemosiderosis (or idiopathic pulmonary hemosiderosis; IPH) is a lung disease of unknown cause that is characterized by alveolar capillary bleeding and accumulation of haemosiderin in the lungs.

However, the major problem with using it as an indicator of hemosiderosis is that it can be elevated in a range of other medical conditions unrelated to iron levels including infection, inflammation, fever, liver disease, renal disease and cancer.

Transfusional hemosiderosis is the accumulation of iron in the liver and/or heart but also endocrine organs, in patients who receive frequent blood transfusions (such as those with thalassemia, sickle cell disease, aplastic anemia or myelodysplastic syndrome).

HH bronze diabetes classic hemochromatosis HFE-related hemochromatosis hemochromatosis type I hemosiderosis primary hemochromatosis None Hereditary hemochromatosis is a general term for several rare genetic disorders that are characterized by the accumulation of iron in various organs of the body such as the liver, heart and pancreas.