Tension-type headache as the unique pain experience of a patient with congenital insensitivity to pain

被引:18
作者
Danziger, N
Willer, JC
机构
[1] Ctr Hosp Univ, Dept Clin Neurophysiol, Paris, France
[2] Ctr Hosp Univ, Consultat Douleur, Paris, France
[3] Ctr Hosp Univ, INSERM, U713, Paris, France
关键词
D O I
10.1016/j.pain.2005.07.012
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
Congenital insensitivity to pain (CIP) is a rare clinical syndrome characterized by dramatic impairment of pain perception since birth and is generally caused by a hereditary sensory and autonomic neuropathy (HSAN) with loss of the small-calibre, nociceptive nerve fibres. We report the case of a 32-year-old woman with CIP and a presumptive diagnosis of HSAN type V, who experienced physical pain for the first and unique time in her life shortly after the sudden loss of her brother. This patient had sustained innumerable painless injuries during childhood, including bone fractures and severe bums. The only pain she ever felt consisted in an intense headache, which took place in a context of strong emotional overload and anxiety, 3 weeks after her younger brother died suddenly in a car accident. The description of this inaugural episode of headache fulfilled the diagnostic criteria of episodic tension-type headache. This case strongly suggests that the transcription of the grief of bereavement into physical pain may sometimes occur independently of the peripheral mechanisms of nociception and despite the lack of previous pain experience. In the light of recent experimental data showing that the same neural mechanisms that regulate physical pain may also control the expression of separation distress and the feeling of social exclusion, this unique case helps to better understand why some patients may feel physically hurt after the loss of someone they love. (c) 2005 International Association for the Study of Pain. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:478 / 483
页数:6
相关论文
共 60 条
[1]   Chronic tension-type headache in children and adolescents [J].
Abu-Arafeh, I .
CEPHALALGIA, 2001, 21 (08) :830-836
[2]   Familial dysautonomia is caused by mutations of the IKAP gene [J].
Anderson, SL ;
Coli, R ;
Daly, IW ;
Kichula, EA ;
Rork, MJ ;
Volpi, SA ;
Ekstein, J ;
Rubin, BY .
AMERICAN JOURNAL OF HUMAN GENETICS, 2001, 68 (03) :753-758
[3]   SPTLC1 is mutated in hereditary sensory neuropathy, type 1 [J].
Bejaoui, K ;
Wu, CY ;
Sheffler, MD ;
Haan, G ;
Ashby, P ;
Wu, LC ;
de Jong, P ;
Brown, RH .
NATURE GENETICS, 2001, 27 (03) :261-262
[4]   Remembering an everyday pain: the role of knowledge and experience in the recall of the quality of dysmenorrhoea [J].
Brodie, EE ;
Niven, CA .
PAIN, 2000, 84 (01) :89-94
[5]  
Chassande B, 1996, REV NEUROL, V152, P623
[6]  
COHEN L D, 1955, J Abnorm Psychol, V51, P333, DOI 10.1037/h0041718
[7]   AUTOSOMAL DOMINANT INSENSITIVITY TO PAIN WITH HYPERPLASTIC MYELINOPATHY AND AUTOSOMAL DOMINANT INDIFFERENCE TO PAIN [J].
COMINGS, DE ;
AMROMIN, GD .
NEUROLOGY, 1974, 24 (09) :838-848
[8]   Pain mechanisms: Labeled lines versus convergence in central processing [J].
Craig, AD .
ANNUAL REVIEW OF NEUROSCIENCE, 2003, 26 :1-30
[9]   HEAT AND MECHANICAL HYPERALGESIA INDUCED BY CAPSAICIN - CROSS MODALITY THRESHOLD MODULATION IN HUMAN C-NOCICEPTORS [J].
CULP, WJ ;
OCHOA, J ;
CLINE, M ;
DOTSON, R .
BRAIN, 1989, 112 :1317-1331
[10]   Mutations in SPTLC1, encoding serine palmitoyltransferase, long chain base subunit-1, cause hereditary sensory neuropathy type I [J].
Dawkins, JL ;
Hulme, DJ ;
Brahmbhatt, SB ;
Auer-Grumbach, M ;
Nicholson, GA .
NATURE GENETICS, 2001, 27 (03) :309-312