Hyperparathyroidism Jaw Tumor Syndrome: A Case Report

Hyperparathyroidism Jaw Tumor Syndrome: A Case Report


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دانشگاه علوم پزشکی تبریز
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نویسندگان: اسماعیل قره پاپاق , سحر رضائی

عنوان کنگره / همایش: 36th Annual Congress of the European Association of Nuclear Medicine , Austria , وین , 2023

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نویسنده ثبت کننده مقاله سحر رضائی
مرحله جاری مقاله تایید نهایی
دانشکده/مرکز مربوطه دانشکده پزشکی
کد مقاله 82694
عنوان فارسی مقاله Hyperparathyroidism Jaw Tumor Syndrome: A Case Report
عنوان لاتین مقاله Hyperparathyroidism Jaw Tumor Syndrome: A Case Report
نوع ارائه پوستر
عنوان کنگره / همایش 36th Annual Congress of the European Association of Nuclear Medicine
نوع کنگره / همایش بین المللی
کشور محل برگزاری کنگره/ همایش Austria
شهر محل برگزاری کنگره/ همایش وین
سال انتشار/ ارائه شمسی 1402
سال انتشار/ارائه میلادی 2023
تاریخ شمسی شروع و خاتمه کنگره/همایش 1402/06/18 الی 1402/06/22
آدرس لینک مقاله/ همایش در شبکه اینترنت
آدرس علمی (Affiliation) نویسنده متقاضی Department of Nuclear Medicine, Medical School, Tabriz University of Medical Sciences, Tabriz, Iran

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نویسنده نفر چندم مقاله
اسماعیل قره پاپاقاول
سحر رضائیدوم

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عنوان متن
خلاصه مقالهA 37-year-old female with complication of a large mass in her right mandible, which may have originated from the parathyroid gland. According to her CT scan, there was an expansible lesion in her mandible body, measuring 80x55 mm, extended to the lower ramus, resulting in the displacement of her inferior alveolar nerve canal to the superior and medial sides. Two possible diagnoses were considered: intraosseous atypical form of neurofibroma, and ossifying fibroma. Biopsy results of this mass showed a vascular myxoid spindle cell lesion, and it was recommended to repeat it due to the incompleteness of the biopsy sample. During the blood test on the patient, Ca=9.2, P=2.5, and PTH=629 were detected. A repeat test after an interval of eight days showed Ca=9.8, iPTH= 738, and VitD3=8. Testing results led to a request for parotid scanning by SPECT method using 99mTc-MIBI. Following intravenous injection of 15 mci of the radiotracer, the patient's neck and mandible were scanned in planar and SPECT modes at 15 and 120 min intervals (early and delayed phases). According to the parathyroid scan, the lower part of the Left thyroid’s lobe showed focally increased uptake, which also retention of the radiotracer in delayed images. The right mandible mass also displayed irregular increased uptake with deformity. According to the scan findings, highly probability of parathyroid adenoma in the left lower lobe, as well as, expansible tumoral involvement in the right mandible with MIBI avid pattern was highly supposed. The probable final diagnosis was hyperparathyroidism jaw tumor syndrome. Afterward, the patient underwent parathyroidectomy and jaw mass resection. As a result of the pathology report, parathyroid carcinoma was diagnosed.
کلمات کلیدیHyperparathyroidism,Jaw Tumor Syndrome,SPECT imaging

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EPOST_EANM23_EGharehpapagh_2.pdf1402/07/11380467دانلود
CR-2.pdf1402/07/1169218دانلود