Secondary hyperparathyroidism is one of the most common complications of ch
ronic renal failure (CRF). Its pathogenesis is multifactorial and still not
completely understood. Pathological mechanism of hypocalcemia, hyperphosph
atemia and calcitriol deficiency are basic characteristics of CRF and main
reason for morphological changes in parathyroid glands and hyperparathyroid
ism (HP). We present a case of a female patient born in 1975. At the age of
10, a urinary infection was diagnosed for the first time and treated. Six
years later, a's nausea and vomiting started, CRF based on bilateral reflux
was diagnosed and the patient. was included in the hemodialysis treatment.
The patient was again examined in 1997, when biochemical parameters, inclu
ding the level of parathyroid hormone, ultrasonography of the neck, scintig
raphy of the skeleton and densitometry, revealed secondary HP. Parathyreoid
ectomy was performed in 1998. During the, follow up period, a tumefaction o
n, a ramus mandibulae dex. was noticed, which was cytologically diagnosed a
s osteitis fibrosa, "brown tumor", a rare complication of the secondary HP.
Surgery was performed and PHD was granuloma gigantocelulare. Prevention an
d therapy of secondary HP is a problem that demands early actions to avoid
possible complications.