Fibrous Dysplasia Polyostotic: When Radiology Clarifies the Diagnosis

被引：0

作者：

Lahlou, Ihssane ^{[1
]}

Essetti, Sara ^{[1
]}

Obilat, Samia ^{[1
]}

Chait, Fatima ^{[1
]}

Bahlouli, Nourrelhouda ^{[1
]}

Guelzim, Yousra ^{[1
]}

El Haddad, Siham ^{[1
]}

Allali, Nazik ^{[1
]}

Chat, Latifa ^{[1
]}

机构：

[1] Ibn Sina Univ Hosp Ctr, Dept Radiol, rue oujda immeuble 6 appartement 6 HASSAN,, Rabat 10020, Rabat Sale Keni, Morocco

来源：

GLOBAL PEDIATRIC HEALTH | 2024年 / 11卷

关键词：

fibrous dysplasia; polyostotic form; rare disease; medical imaging; STIMULATORY G-PROTEIN; ACTIVATING MUTATIONS;

D O I：

10.1177/2333794X241251746

中图分类号：

R72 [儿科学];

学科分类号：

100202 ;

摘要：

Fibrous dysplasia is a rare non-hereditary congenital condition characterized by 2 main forms: monostotic and polyostotic. Monostotic is the more common form, while polyostotic, often associated with a syndrome, is rarer. The case presented involves a 10-year-old patient who was diagnosed with polyostotic fibrous dysplasia accompanied by an endocrinopathy. This report explores the clinical and radiological aspects of this condition based on the patient's case.

引用

页数：7

共 9 条

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