18F-FDG PET/CT in the Hyperparathyroidism-Jaw-Tumor Syndrome

被引：2

作者：

Nazerani Hooshmand, Tina ^{[1
]}

Pernthaler, Birgit ^{[1
]}

Szurian, Kinga ^{[2
]}

Pau, Mauro ^{[3
]}

Aigner, Reingard Maria ^{[1
]}

机构：

[1] Med Univ Graz, Dept Radiol, Div Nucl Med, Auenbruggerpl 9A, A-8036 Graz, Austria

[2] Med Univ Graz, Diagnost & Res Inst Pathol, Graz, Austria

[3] Med Univ Graz, Dept Dent Med & Oral Hlth, Div Oral Maxillofacial Surg, Graz, Austria

来源：

CLINICAL NUCLEAR MEDICINE | 2021年 / 46卷 / 06期

关键词：

F-18 FDG PET/CT; hyperparathyroidism; jaw-tumor syndrome; jaw-ossifying fibroma; parathyroid adenoma; HEREDITARY HYPERPARATHYROIDISM;

D O I：

10.1097/RLU.0000000000003625

中图分类号：

R8 [特种医学]; R445 [影像诊断学];

学科分类号：

1002 ; 100207 ; 1009 ;

摘要：

Hyperparathyroidism-jaw-tumor syndrome (HPT-JTS) is a rare autosomal dominant disorder. A typical manifestation of HPT-JTS is the association of jaw-ossifying fibroma with primary hyperparathyroidism. Due to its rarity and diversity in its manifestations, it is a challenging diagnosis. A 33-year-old woman was referred due to painful swelling of the right maxilla suggestive of malignancy. The clinical presentations were not conclusive until she underwent F18-fluorodeoxyglucose positron emission tomography/computed tomography (F18-FDG PET/CT). F18-FDG PET/CT proved to be a useful tool to assist the clinicians in visualizing the "bigger picture" and, therefore all manifestation as pieces of "one puzzle."

引用

页码：497 / 498

页数：2

共 8 条

[1] Hyperparathyroidism-jaw tumor syndrome in Roma families from Portugal is due to a founder mutation of the HRPT2 gene [J].

Cavaco, BM ;

Guerra, L ;

Bradley, KJ ;

Carvalho, D ;

Harding, B ;

Oliveira, A ;

Santos, MA ;

Sobrinho, LG ;

Thakker, RV ;

Leite, V .

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2004, 89 (04) :1747-1752

[2] Hyperparathyroidism-jaw tumour syndrome [J].

Chen, JD ;

Morrison, C ;

Zhang, C ;

Kahnoski, K ;

Carpten, JD ;

Teh, BT .

JOURNAL OF INTERNAL MEDICINE, 2003, 253 (06) :634-642

[3] Parathyroid adenoma presented with multiple brown tumors and nephrocalcinosis [J].

Eklioglu, Beray Selver ;

Atabek, Mehmet Emre ;

Akyurek, Nesibe .

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM, 2013, 26 (3-4) :213-214

[4] CDC73-related hereditary hyperparathyroidism: five new mutations and the clinical spectrum [J].

Frank-Raue, Karin ;

Haag, Christine ;

Schulze, Egbert ;

Keuser, Roger ;

Raue, Friedhelm ;

Dralle, Henning ;

Lorenz, Kerstin .

EUROPEAN JOURNAL OF ENDOCRINOLOGY, 2011, 165 (03) :477-483

[5] Hyperparathyroidism [J].

Fraser, William D. .

LANCET, 2009, 374 (9684) :145-158

[6]

JACKSON CE, 1990, SURGERY, V108, P1006

[7]

Piciu Doina, 2016, Clujul Med, V89, P555

[8] Clinical Features, Treatment, and Surveillance of Hyperparathyroidism-Jaw Tumor Syndrome: An Up-to-Date and Review of the Literature [J].

Torresan, Francesca ;

Iacobone, Maurizio .

INTERNATIONAL JOURNAL OF ENDOCRINOLOGY, 2019, 2019

← 1 →