Title of article :
Primary Hyperparathyroidism Misdiagnosed as Giant Cell Bone Tumor of
Maxillary Sinus: A Case Report
Author/Authors :
Aghaghazvini، Leila نويسنده , , Sharifian، Hashem نويسنده Department of Radiology, Amiralam Hospital, Tehran
University of Medical Sciences, Tehran, Iran , , RASULI، Bahman نويسنده Hamadan University of Medical Sciences, Besat Hospital. Hamadan, Iran ,
Issue Information :
فصلنامه با شماره پیاپی 0 سال 2016
Abstract :
Primary hyperparathyroidism is an endocrine disorder recognized by
hyperfunction of parathyroid gland, which can result in persistent bone
absorption and brown tumor. Facial involvement of brown tumor is rare
and usually involves the mandible. Giant cell tumor ( GCT) is an
expansile osteolytic bone tumor which is very similar in clinical,
radiological and histological features to brown tumor. Herein, we
present a 35-year-old woman with an 11-month history of gradually
swelling of the right maxilla and buccal spaces began during pregnancy
two years ago. No other clinical or laboratory problems were detected.
Postpartum CT scan demonstrated a lytic expansile multi-septated mass
lesion containing enhancing areas, which initially described as GCT of
the right maxillary sinus following surgery. Four months later, gradual
progressive swelling of the bed of tumor was recurred and revised
pathological slices were compatible with GCT. Regarding patient recent
paresthesia, repeated laboratory tests were performed. Finally,
according to laboratory results (elevation of serum calcium and
parathyroid hormone), ultrasonographic findings and radioisotope scan
(Sestamibi), probable parathyroid mass and brown tumor of maxilla was
diagnosed. Pathology confirmed hyperplasia of right inferior parathyroid
gland. Our case was thought-provoking due to its interesting clinical
presentation and unusual presentation of brown tumor in parathyroid
hyperplasia.
Journal title :
Iranian Journal of Radiology (IJR)
Journal title :
Iranian Journal of Radiology (IJR)