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先天性无痛觉与无汗症(CIPA)综合征;4例报告

Congenital Insensitivity to Pain and Anhydrosis (CIPA) Syndrome; A Report of 4 Cases.

作者信息

Daneshjou Khadije, Jafarieh Hanieh, Raaeskarami Seyed-Reza

机构信息

Department of Pediatrics, Imam Komoini Hospital, Tehran University of Medical Sciences, Tehran, Iran.

出版信息

Iran J Pediatr. 2012 Sep;22(3):412-6.

Abstract

BACKGROUND

Congenital insensitivity to pain with anhidrosis (CIPA) is characterized by recurrent episodes of infections and unexplained fever, anhidrosis (inability to sweat), and absence of reaction to noxious stimuli, self-mutilating behavior, mental retardation and damages to oral structures.

CASE PRESENTATION

In this article, we have demonstrated the signs and symptoms of 4 children that refer to the pediatrics department of the Imam Khomeini hospital and assay about their complications with this disease. They mostly presented by recurrent osteomyelitis in their feet that severely controlled by antibiotic therapy and even surgery. They had no pain sensation in spite of deep sore and infection.

CONCLUSION

This syndrome can be diagnosed by clinical and paraclinical tests together but it would be better to confirm by genetic test. The diagnosis of this syndrome helps us to try for the better quality of life for the patients and avoid unnecessary amputations.

摘要

背景

先天性无痛觉伴无汗症(CIPA)的特征为反复感染发作、不明原因发热、无汗(无法出汗)、对有害刺激无反应、自残行为、智力迟钝以及口腔结构受损。

病例报告

在本文中,我们展示了4名转诊至伊玛目霍梅尼医院儿科的儿童的体征和症状,并分析了他们患此病的并发症。他们大多表现为足部反复骨髓炎,通过抗生素治疗甚至手术得到了有效控制。尽管有深部溃疡和感染,但他们没有疼痛感。

结论

该综合征可通过临床和辅助检查共同诊断,但最好通过基因检测来确诊。该综合征的诊断有助于我们为患者争取更好的生活质量,避免不必要的截肢。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d722/3564101/96c8ee23d2a6/IJPD-22-412-g001.jpg

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