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Tunisie Medicale 2008-Sep

[Osteomalacia and giant cell tumor: a rare case].

Watumiaji waliosajiliwa tu ndio wanaweza kutafsiri nakala
Ingia / Ingia
Kiungo kimehifadhiwa kwenye clipboard
Hela Sehli
Lilia Daoud
Rim Ben Mbarek
Rim Ghorbel
Kaouther Ben Abdelghani
Hichem Charfi
Ilhem Cheour
Lamjed Tarhouni
Slaheddine Sellami

Maneno muhimu

Kikemikali

BACKGROUND

Oncogenic octeomalacia is an unusual and rare clinicopathologic syndrome characterized by mesenchymal tumors that apparently produce osteomalacia and biochemical abnormalities consisting of hypophosphatemia and normocalcemia.

OBJECTIVE

We have investigated the mechanism by which a giant cell tumor of bone caused biopsy-proved osteomalacia in a 50-year-old woman.

METHODS

A 50-year-old woman presented with generalized bone and pelvicrural pain, associated with fatiguability and muscle weakness. The diagnosis of osteomalacia was retained, associated with a giant cell tumor. The coexistence of giant cell tumor of bone and osteomalacia suggested the diagnosis of oncogenic osteomalacia. Resolution of the biochemical abnormalities of the syndrome after tumor resection, established this diagnosis.

CONCLUSIONS

oncogenic osteomalacia can be a form of vitamin-D-refractory osteomalacia due to altered vitamin D3 metabolism.

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