A Case Report of Blau Syndrome
10.12376/j.issn.2097-0501.2023.04.012
- VernacularTitle:Blau综合征一例
- Author:
Guozhuang LI
1
,
2
;
Kexin XU
1
,
2
;
Sen ZHAO
1
,
2
;
Jianguo ZHANG
1
,
2
,
3
;
Guixing QIU
1
,
2
,
3
;
Ruifang SUI
2
,
4
;
Tao WANG
2
,
5
;
Min SHEN
2
,
6
;
Xuejun ZENG
2
,
7
;
Wei WANG
2
,
8
;
Mingsheng MA
2
,
8
;
Min WEI
2
,
8
;
Xiao LONG
2
,
9
;
Ke LYU
2
,
10
;
Li HUO
2
,
11
;
Lei XUAN
1
,
2
,
12
;
Nan WU
1
,
2
,
3
Author Information
1. Department of Orthopaedic Surgery, Beijing Key Laboratory for Genetic Research of Skeletal Deformity, Key Laboratory of Big Data for Spinal Deformities, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences &
2. Peking Union Medical College, Beijing 100730, China.
3. Peking Union Medical College, Beijing 100730, China.State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences &
4. Department of Ophthalmology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences &
5. Department of Dermatology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences &
6. Department of Rheumatology and Immunology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences &
7. Department of General Practice, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences &
8. Department of Pediatrics, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences &
9. Department of Plastic and Reconstructive Surgery, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences &
10. Department of Ultrasound Medicine, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences &
11. Department of Nuclear Medicine, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences &
12. Peking Union Medical College, Beijing 100730, China.Department of Traditional Chinese Medicine, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences &
- Publication Type:Journal Article
- Keywords:
Blau syndrome;
joint swelling;
uveitis;
steroid treatment
- From:
JOURNAL OF RARE DISEASES
2023;2(4):547-553
- CountryChina
- Language:Chinese
-
Abstract:
Blau syndrome is a rare genetic disorder characterized by the a mix of granulomatous arthritis, uveitis, and dermatitis. Patients typically manifest multisystem involvement, including ocular, skin, and skeletal abnormalities. Blau syndrome is extremely rare, with a global incidence of less than one in a million among children. In this multidisciplinary consultation, we present a case of a 21-year-old young female patient having multisystemic involvement since early childhood. She was presented with multiple joint swelling, skin lesions, increased eye discharge, and accompanied by hypertension and arterial abnormalities, and received a diagnosis of uveitis. The patient had been receiving steroid treatment since the age of 6 and has tried various medications, with some improvement in joint swelling and ocular symptoms. Through this rare disease multidisciplinary consultation, we aim to provide guidance in the molecular diagnosis of the patient, multisystem assessment, and the selection and formulation of treatment plans. Additionally, we hope that by reporting this case, clinical physicians can gain a better understanding of the diagnosis and comprehensive treatment strategies for Blau syndrome, thereby improving the management and treatment of rare diseases.
