|
|
|
| Multiple intracerebral calcification: case report and differential diagnosis |
| LIN Jia1 LIU Jialin2 |
1.The Second Department of Neurosurgery, Jilin Central Hospital, Jilin Province, Jilin 132001, China;
2.Department of Neurosurgery, Dongfang Hospital of Beijing University of Chinese Medicine, Beijing 100078, China |
|
|
|
Abstract Pseudohypoparathyroidism is a rare genetic disease, in which, the X chromosome has multiple genes with dominant heredity and is accompanied by autosomal dominant or recessive inheritance in some cases. The clinical manifestations are complex and diverse, especially cases with intracerebral calcification and characteristic manifestations of the nervous system are often misdiagnosed as other diseases. This article reports one patient with head trauma who checked the head CT showed multiple calcifications in the brain. After the consultation of Department of Endocrinology, the patient′s diagnosis was clearly defined, and the patient′s examination results, condition, and treatment process were discussed. Finally, the paper summarizes the clinical differential diagnosis of these diseases.
|
|
|
|
|
|
[1] Donghi V，Mora S，Zamproni I，et al. Pseudohypoparathyroidism，an often delayed diagnosis：a case series [J]. Cases J，2009，2：6734.
[2] Sunder RA，Sinqh M. Pseudohypoparathyroidism：a series of three cases and an unusual presentation of ocular tetany [J]. Anaesthesia，2006，61（4）：394-398.
[3] 魏丁，梁立阳，孟哲.小儿假性甲状旁腺功能减退症的临床研究[J].中国临床研究杂志，2005，4（3）：32-34.
[4] 杨纲.内分泌生理与病理卫生学[M].天津：天津科学技术出版社，1996：376-409.
[5] 张婷婷，母义明，吕朝晖，等.假性甲状旁腺功能减退症的临床研究[J].军医进修学院学报，2009，30（5）：643-645.
[6] 罗成，张素华.假性甲状旁腺功能减退症误诊为Fahr综合征1例并文献复习[J].重庆医学，2009，9（38）：2284-2285.
[7] Bastepe M，Jüppner H. GNAS locus and pseudohypoparathyroidism [J]. Horm Res，2005，63（2）：65-74.
[8] 刘琦，李海花.甲状旁腺功能减退脑内钙化并癫痫发作1例[J].实用医学杂志，2014，30（7）：1167.
[9] 徐少明.甲状旁腺功能减退的诊断与治疗[J].中国实用外科杂志，2008，28（3）：182-184.
[10] 洪璧楷，代海洋，林枫枫，等.结节性硬化症的CT和磁共振成像诊断价值[J].实用医学影像杂志，2013，14（6）：405-407.
[11] Yates JR，Maclean C，Higgins JN，et al. The tuberculosis sclerosis 2000 study：presentation，initial assessments and implantations for diagnosis and management [J]. Arch Dis Child，2011，96（11）：1020-1025.
[12] 李睿婷.特发性基底节钙化的研究进展[J].疑难病杂志，2014，13（8）：862-865.
[13] 钟心，朱廷敏，潘桂芬，等.Fahr病的CT诊断（附11例报告）[J].中华放射学杂志，1998，32（2）：122-123.
[14] Benke T，Karner E，Seppi E，et al. Subacute dementia and imaging correlates in a case of Fahr′s disease [J]. J Neurol Neurosurg Psychiatry，2004，75（8）：1163-1165.
[15] 陈建华.家族性特发性基底节钙化的CT表现[J].实用医学影像杂志，2011，12（3）：140-144.
[16] Meeks M，Bush A. Primary Ciliary Dyskinesia（PCD）[J]. Ped Pulmonol，2015，29（4）：307-316.
[17] 孙彦华，王昕，高蓓兰，等.Kartageners综合征15例回顾分析[J].中国实用医药，2008，3（3）：32-33.
[18] Yamada N，Hayashi T. Asymptomatic familial basal ganglia calcification with autosomal dominant inheritance：a family report [J]. No To Hattatsu，2000，32（6）：515.
[19] Sanchetee P，Venkataraman S，Mohan C，et al. Basal ganglia calcification [J]. J Assoc Physicians India，1999，47（5）：507-509.
[20] 屈传强，郭洪志.特发性非家族性大脑基底节钙化的CT与临床[J].临床神经病学杂志，2003，16（4）：235-236.
[21] 苗海锋，石涛，肖卫民，等.Klinefelter综合征伴颅内多发钙化1例[J].中国神经精神疾病杂志，2011，37（2）：120-121. |
|
|
|
