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Case of progressive facial hemiatrophy with cervical sympathetic hyperactivity as underlying aetiology

Published online by Cambridge University Press:  15 June 2012

H Monobe ,
K Miyano ,
R Kagoya  and
H Tojima
H Monobe*
Affiliation:
Department of Otolaryngology, Hitachi General Hospital, Ibaraki, Japan Department of Otolaryngology, NTT Medical Center Tokyo, Tokyo, Japan
K Miyano
Affiliation:
Department of Otolaryngology, Showa General Hospital, Tokyo, Japan
R Kagoya
Affiliation:
Department of Otolaryngology, Tokyo Metropolitan Tama Medical Center, Tokyo, Japan
H Tojima
Affiliation:
Department of Otolaryngology, Hitachi General Hospital, Ibaraki, Japan
*
Address for correspondence: Dr Hiroko Monobe, Department of Otolaryngology, NTT Medical Center Tokyo, 5-9-22, Higashigotanda, Shinagawa, Tokyo, 141-8625, Japan Fax: +81 3 3448 6582 E-mail: [email protected]
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Abstract

Objective:

We report a case of progressive facial hemiatrophy with cervical sympathetic hyperactivity as a possible underlying aetiology, based on clinical findings, three-dimensional computed tomography and thermographic imaging.

Methods:

We present a case report in which we describe the investigation and clinical course of progressive facial hemiatrophy, and we also review the world literature on this condition.

Results:

To our knowledge, this is the first report in the world literature of progressive facial hemiatrophy with cervical sympathetic hyperactivity indicated as a possible underlying aetiology, based on clinical findings, three-dimensional computed tomography and thermographic imaging.

Conclusion:

This syndrome may lead to atrophy of the subcutaneous adipose tissue with hyperfunction of the vegetative system. Although this is a rare syndrome, otolaryngologists should be aware of its symptoms, aetiology and treatment.

Keywords

Progressive Facial HemiatrophyParry-Romberg DiseaseSympathetic Nervous SystemSympathectomyThermography
Type
Clinical Records
Information
The Journal of Laryngology & Otology , Volume 126 , Issue 7 , July 2012 , pp. 725 - 728
Copyright
Copyright © JLO (1984) Limited 2012

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References

1Singh, G, Bajpai, HS. Progressive facial hemiatrophy. Dermatologica 1969;138:288–91CrossRefGoogle ScholarPubMed
2Pensler, JM, Murphy, GF, Mulliken, JB. Clinical and ultrastructural studies of Romberg's hemifacial atrophy. Plast Reconstr Surg 1990;85:669–76CrossRefGoogle ScholarPubMed
3Mazzeo, N, Fisher, JG, Mayer, MH, Mathieu, GP. Progressive hemifacial atrophy (Parry-Romberg syndrome). Case report. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 1995;79:30–5CrossRefGoogle ScholarPubMed
4Abele, DC, Bedingfield, RB, Chandler, FW, Given, KS. Progressive facial hemiatrophy (Parry-Romberg syndrome) and borreliosis. J Am Acad Dermatol 1990;22:531–3CrossRefGoogle ScholarPubMed
5Moss, ML, Crikelair, GF. Progressive facial hemiatrophy following cervical sympathectomy in the rat. Arch Oral Biol 1960;1:254–8CrossRefGoogle ScholarPubMed
6Scope, A, Barzilai, A, Trau, H, Orenstein, A, Winkler, E, Haik, J. Parry-Romberg syndrome and sympathectomy – a coincidence? Cutis 2004;73:343–4, 346Google ScholarPubMed
7Carreno, M, Donaire, A, Barcelo, MI, Rumia, J, Falip, M, Agudo, R et al. Parry Romberg syndrome and linear scleroderma in coup de sabre mimicking Rasmussen encephalitis. Neurology 2007;68:1308–10CrossRefGoogle ScholarPubMed
8Sakuraoka, K, Tajima, S, Nishikawa, T. Progressive facial hemiatrophy: report of five cases and biochemical analysis of connective tissue. Dermatology 1992;185:196–201CrossRefGoogle ScholarPubMed
9Moore, MH, Wong, KS, Proudman, TW, David, DJ. Progressive hemifacial atrophy (Romberg's disease): skeletal involvement and treatment. Br J Plast Surg 1993;46:39–44CrossRefGoogle ScholarPubMed
10Guerrerosantos, J, Guerrerosantos, F, Orozco, J. Classification and treatment of facial tissue atrophy in Parry-Romberg disease. Aesthetic Plast Surg 2007;31:424–34CrossRefGoogle ScholarPubMed
11Rees, TD. Facial, atrophy. Clin Plast Surg 1976;3:637–46CrossRefGoogle Scholar
12Jablonska, S. Facial hemiatrophy and its relation to localized scleroderma. In: Jablonska, S, ed. Scleroderma and Pseudoscleroderma, 2nd edn.Warsaw: Polish Med, 1975;537–48Google Scholar
13Wartenberg, R. Progressive facial hemiatrophy. Arch Neurol Psychiatry 1945;54:75–96CrossRefGoogle Scholar
14Togari, A, Arai, M. Pharmacological topics of bone metabolism: the physiological function of the sympathetic nervous system in modulating bone resorption. J Pharmacol Sci 2008;106:542–6CrossRefGoogle Scholar
15Kawano, Y, Araki, E, Arakawa, K, Matsumono, S, Yamada, T, Kira, J. A case of progressive hemifacial atrophy with Pourfourde Petit syndrome which was successfully treated by stellate ganglion block [in Japanese]. Rinsho Shinkeigaku 1999;39:731–4Google ScholarPubMed
16Aouba, A, Der Agopian, P, Genty-Le Goff, I, Mutschler, C, Janin, N, Patri, B. Pourfour du Petit syndrome: a rare aetiology of unilateral exophthalmos with mydriasis and lid retraction. Rev Med Interne 2003;24:261–5CrossRefGoogle ScholarPubMed
17Ségura, P, Speeg-Schatz, C, Wagner, JM, Kern, O. Claude Bernard-Horner syndrome and its opposite, Pourfour du Petit syndrome, in anesthesia and intensive care [in French]. Ann Fr Anesth Reanim 1998;17:709–24CrossRefGoogle ScholarPubMed
18Yokoyama, K, Sugiyama, K. Temporomandibular joint pain analgesia by linearly polarized near-infrared irradiation. Clin J Pain 2001;17:41–5CrossRefGoogle ScholarPubMed
19Wajima, Z, Shitara, T, Inoue, T, Ogawa, R. Linear polarized light irradiation around the stellate ganglion area increases skin temperature and blood flows [in Japanese]. Masui 1996;45:433–8Google Scholar