2004
DOI: 10.5414/cnp61289
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Brown tumors developing in renal transplant recipients with persistent hyperparathyroidism: 2 case reports and review of literature

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Cited by 8 publications
(5 citation statements)
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“…Brown tumors, a late manifestation of secondary hyperparathyroidism, are due to bone microfractures with subsequent bleeding causing localized osteoclast influx, osteolysis, and subsequent reactional medullar fibrosis and leading to the constitution of tumoral brown masses because of haemosiderin deposits [9]. In our patient, total body bone scintigraphy did not show increased uptake by the mandibular OF, an argument against a brown tumor.…”
Section: Discussionmentioning
confidence: 53%
“…Brown tumors, a late manifestation of secondary hyperparathyroidism, are due to bone microfractures with subsequent bleeding causing localized osteoclast influx, osteolysis, and subsequent reactional medullar fibrosis and leading to the constitution of tumoral brown masses because of haemosiderin deposits [9]. In our patient, total body bone scintigraphy did not show increased uptake by the mandibular OF, an argument against a brown tumor.…”
Section: Discussionmentioning
confidence: 53%
“…Medical intervention of normalizing blood calcium and phosphate levels should stop the progression of a BT. If unsuccessful, a total or subtotal parathyroidectomy is recommended [7]. Our patient was initially managed pharmacologically with cinacalcet, but responded insufficiently.…”
Section: Discussionmentioning
confidence: 92%
“…Therefore, hypersecretion of PTH can be inhibited by eliminating phosphate excess. It can be achieved by oral antacids, dietetic restrictions and peritoneal dialysis or haemodialysis [4,10,11,12]. However, after a certain period of time, the enlarged parathyroid gland might not react to the fluctuant serum calcium level, therefore some degree of autonomous glandular function develops [5,13].…”
Section: Discussionmentioning
confidence: 99%