Brown tumor
Brown tumor | |
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![]() Brown tumours of the hands in a patient with hyperparathyroidism.
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Classification and external resources | |
Specialty | Lua error in Module:Wikidata at line 446: attempt to index field 'wikibase' (a nil value). |
ICD-9-CM | 252.01 |
DiseasesDB | 30721 |
Patient UK | Brown tumor |
MeSH | D010002 |
The brown tumor is a bone lesion that arises in settings of excess osteoclast activity, such as hyperparathyroidism. It is not a true neoplasm, as the term "tumor" suggests; however, it may mimic a true neoplasm.[1] Brown tumours are radiolucent on x-ray.
Contents
Pathology
Brown tumours consist of fibrous tissue, woven bone and supporting vasculature, but no matrix. The osteoclasts consume the trabecular bone that osteoblasts lay down and this front of reparative bone deposition followed by additional resorption can expand beyond the usual shape of the bone, involving the periosteum thus causing bone pain. The characteristic brown coloration results from hemosiderin deposition into the osteolytic cysts. Hemosiderin deposition is not a distinctive feature of brown tumors; it may also be seen in giant cell tumors of the bone.[2][3]
Brown tumors may be rarely associated with ectopic parathyroid adenomas.[4]
Epidemiology
Age and gender have an effect on the incidence of these lesions; they are more prevalent in women than men (though still common in both genders), and they appear more frequently with age. Due to the standard of medical care and screening in developed countries, it is increasingly rare for primary hyperparathyroidism to present with accompanying bone disease. This is not the case in less developed nations, however, and the two conditions are more often seen together.[5]
See also
References
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- ↑ http://www.bonetumor.org/tumors-disorder-metabolism/brown-tumor