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一位 5 岁的巴勒斯坦贝都因女孩反复用手指自残,被诊断为先天性无痛症和无汗症。

A 5-Year-Old Palestinian Bedouin Girl with Repeated Self-Induced Injuries to the Digits, a Diagnosis of Congenital Insensitivity to Pain, and Anhidrosis.

机构信息

Department of Orthopedics, Al-Safa Specialized Hospital, Jarash, Jordan.

Department of Internal Medicine, Faculty of Medicine, Jordan University of Science and Technology, Irbid, Jordan.

出版信息

Am J Case Rep. 2021 Nov 4;22:e933486. doi: 10.12659/AJCR.933486.

DOI:10.12659/AJCR.933486
PMID:34732685
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8579061/
Abstract

BACKGROUND Congenital insensitivity to pain with anhidrosis (CIPA), also referred to as hereditary sensory and autonomic neuropathy type IV, is a rare autosomal recessive disease caused by mutations in the NTRK1 gene. The inability to feel pain and temperature often leads to repeated severe and unintentional self-inflicted injuries; these can result in severe complications, as patients heal slowly from skin and bone injuries. This case report describes a 5-year-old Palestinian girl with self-inflicted injury to the digits, a dislocated distal inter-phalangeal joint of the left big toe, and a diagnosis of CIPA. CASE REPORT A 5-year-old girl, a daughter of related Palestinian Bedouin parents, presented with a chronic unhealed wound over the planter surface of the left foot. Painless repetitive minor traumata over the same area badly affected wound healing and this led to wound dehiscence and dislocation of the distal inter-phalangeal joint of the left big toe. Surgical fixation of the dislocated joint along with intravenous antibiotics and close follow-up resulted in eventual improvement and near complete wound healing despite the obviously slow healing process. The girl also displayed evidence of unintentional self-inflicted injury, which within the overall clinical context warranted a clinical suspicion of CIPA. This was confirmed by genetic testing for the presence of a homozygous frameshift mutation in the NTRK1 gene (c.1842_1843insT; p.Pro615Serfs*12). CONCLUSIONS This case report shows that a physician should have a low threshold of suspicion to investigate for CIPA when managing children with multiple unintentional self-inflicted injuries, anhidrosis, and pain insensitivity, mainly through genetic testing to detect mutations in the NTRK1 gene.

摘要

背景

先天性无痛无汗症(CIPA),也称遗传性感觉自主神经病Ⅳ型,是一种罕见的常染色体隐性遗传病,由 NTRK1 基因突变引起。由于无法感知疼痛和温度,患者常反复遭受严重且无意识的自伤;这些自伤可能导致严重并发症,因为患者的皮肤和骨骼损伤愈合缓慢。本病例报告描述了一名 5 岁巴勒斯坦女孩,因手指自残、左大脚趾远节指间关节脱位,被诊断为 CIPA。

病例报告

一名 5 岁女孩,其父母为巴勒斯坦贝多因近亲,因左足跖部慢性未愈合伤口就诊。同一部位无痛性、重复性轻微创伤严重影响了伤口愈合,导致伤口裂开和左大脚趾远节指间关节脱位。脱位关节的手术固定、静脉内应用抗生素和密切随访,最终导致伤口愈合改善,几乎完全愈合,尽管愈合过程明显缓慢。该女孩还表现出无意识自伤的证据,根据整体临床情况,临床怀疑为 CIPA。通过对 NTRK1 基因(c.1842_1843insT;p.Pro615Serfs*12)存在纯合移码突变的基因检测证实了这一点。

结论

本病例报告表明,当遇到有多处无意识自伤、无汗和痛觉缺失的儿童时,医生应保持高度怀疑,主要通过基因检测来检测 NTRK1 基因突变,以调查 CIPA 的可能性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0f1/8579061/84c6e2bef9ab/amjcaserep-22-e933486-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0f1/8579061/099f802d53cb/amjcaserep-22-e933486-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0f1/8579061/4c7a74a62854/amjcaserep-22-e933486-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0f1/8579061/431e4eefeecd/amjcaserep-22-e933486-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0f1/8579061/84c6e2bef9ab/amjcaserep-22-e933486-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0f1/8579061/099f802d53cb/amjcaserep-22-e933486-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0f1/8579061/4c7a74a62854/amjcaserep-22-e933486-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0f1/8579061/431e4eefeecd/amjcaserep-22-e933486-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0f1/8579061/84c6e2bef9ab/amjcaserep-22-e933486-g004.jpg

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本文引用的文献

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Anesthetic management of children with congenital insensitivity to pain with anhidrosis.先天性无痛觉伴无汗症患儿的麻醉管理
Pediatr Investig. 2019 Oct 28;4(4):296-298. doi: 10.1002/ped4.12152. eCollection 2020 Dec.
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Painless: a case of congenital insensitivity to pain in a 5-year-old male.
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Heterogeneity of clinical features and mutation analysis of in Han Chinese patients with congenital insensitivity to pain with anhidrosis.中国汉族先天性无痛觉伴无汗症患者的临床特征异质性及突变分析
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