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Indian Journal of Dermatology
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Year : 2017  |  Volume : 62  |  Issue : 2  |  Page : 216-217
Hemifacial microsomia and accessory auricles in an adolescent boy


Department of Dermatology, Government Villupuram Medical College, Villupuram, Tamil Nadu, India

Date of Web Publication9-Mar-2017

Correspondence Address:
C Chandrakala
Department of Dermatology, Government Villupuram Medical College, Villupuram, Tamil Nadu
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/ijd.IJD_621_16

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How to cite this article:
Chandrakala C, Kumar P, Karpagam B. Hemifacial microsomia and accessory auricles in an adolescent boy. Indian J Dermatol 2017;62:216-7

How to cite this URL:
Chandrakala C, Kumar P, Karpagam B. Hemifacial microsomia and accessory auricles in an adolescent boy. Indian J Dermatol [serial online] 2017 [cited 2017 Nov 24];62:216-7. Available from: http://www.e-ijd.org/text.asp?2017/62/2/216/201766


Sir,

Goldenhar syndrome is a rare disorder with developmental defects involving the first and second branchial arches being named in the Online Mendelian Inheritance of Man (OMIM) as “hemifacial microsomia” also known as “oculoauriculovertebral syndrome or spectrum.”

A 17-year-old boy presented with multiple bilateral preauricular nodules since birth and swelling in the left eye since childhood which was progressively increasing in size, obscuring the vision. His hearing was normal. There was no maternal illness during pregnancy. On examination, he had epibulbar dermoid in the left eye [Figure 1]a and showed high-arched palate [Figure 1]b and multiple accessory auricles [Figure 1]c and [Figure 1]d. Linear and rectangular atrophic macules were seen over cheeks [Figure 1]c and [Figure 1]d. The atrophic macules appeared spontaneously without any history of inflammation or trauma. Flattening of the face was noted on the left side with micrognathia and macrostomia [Figure 2]. Audiogram was normal. X-ray and computed tomography scan of the cervical spine showed block vertebra between C5, C6 level [Figure 3]a.
Figure 1: (a) Epibulbar dermoid in the left eye. (b) High-arched palate. (c) Accessory auricles around left ear with atrophic macules over the cheek (black arrows). (d) Accessory auricles around the right ear, atrophic macules over the cheek (black arrows), and micrognathia

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Figure 2: Hemifacial microsomia on the left side with micrognathia and macrostomia

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Figure 3: (a) Computed tomography of the cervical spine showing block vertebra at C5, C6 level. (b) X-ray of the thoracolumbar spine showing hemivertebra at L5 level

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X-ray of the thoracolumbar spine showed hemivertebra at L5 level with left-sided lumbar scoliosis [Figure 3]b. There were no cardiac anomalies, and ultrasonogram of the abdomen was normal.

”Oculoauriculovertebral spectrum” was described by Goldenhar in 1952 with the triad of ear defects, epibulbar dermoids, and vertebral anomalies.[1]

 Goldenhar-Gorlin syndrome More Details is an expanded form of Goldenhar syndrome associated with facial clefting, mental retardation, vertebral abnormalities, cardiac or pulmonary anomalies, hemifacial microsomia involving hypoplasia of the maxilla, mandible, zygomatic bones, muscles of mastication, and facial expression.[2] Most cases of Goldenhar syndrome are sporadic.

The etiology is multifactorial with interaction between genetic and environmental factors such as exposure to chemicals or viruses during pregnancy and nutritional factors which may interfere with the development of vertebral and branchial systems.[3],[4] Other manifestations of this syndrome include microtia, accessory auricles, preauricular pits or sinuses, lipodermoids, coloboma, microphthalmia, strabismus, failure of segmentation of vertebra, hemivertebra, cuneiform vertebra, and occipitalization of  Atlas More Details.[5]

Other reported anomalies are club foot, congenital dislocation of the hip, Sprengel's deformity, radial limb defects, rib abnormalities, mandibular hypoplasia, cleft palate, occult spinal dysraphism, conductive or sensory neural hearing loss,[6] atrial or ventricular septal defects, coarctation of aorta, patent ductus arteriosus, and tetralogy of Fallot.[7]

The other syndromes resulting from defective development of the first and second branchial arches are  Treacher Collins syndrome More Details and Hallermann–Streiff syndrome.

The differential diagnoses for cystic eye lesions are Delleman syndrome and sebaceous nevus, central nervous system malformations, aplasia cutis congenita, limbal dermoid, and pigmented giant nevus with neurocutaneous melanosis syndrome.

Accessory auricles and preauricular sinuses occur with Treacher Collins, Goldenhar, Nager's acrofacial dysostosis, 4p-, oculocerebrocutaneous, Kabuki's, Townes-Brocks, Haberland, and branchio-oto-renal syndromes.

Our patient presented with classical features of Goldenhar syndrome, for whom multidisciplinary surgical corrections and regular follow-up are being planned. There are about 3% chances of passing it on to the off springs. Goldenhar syndrome support system can help patients and parents. Atrophic macules in Goldenhar syndrome have not been reported in the literature so far.

Whether the atrophic macules over the face were due to atrophia maculosa varioliformis cutis or an association with Goldenhar syndrome is not known.

Declaration of patient consent

The authors certify that they have obtained all appropriate patient consent forms. In the form the patient(s) has/have given his/her/their consent for his/her/their images and other clinical information to be reported in the journal. The patients understand that their names and initials will not be published and due efforts will be made to conceal their identity, but anonymity cannot be guaranteed.

Financial support and sponsorship

Nil.

Conflicts of interest

There are no conflicts of interest.

 
   References Top

1.
Vinay C, Reddy RS, Uloopi KS, Madhuri V, Sekhar RC. Craniofacial features in Goldenhar syndrome. J Indian Soc Pedod Prev Dent 2009;27:121-4.  Back to cited text no. 1
[PUBMED]  [Full text]  
2.
Gorlin RJ, Cohen MM Jr., Levin LS. Oculoauriculovertebral spectrum. In: Syndromes of the Head and Neck. 3rd ed. New York: Oxford University Press; 1990. p. 641-9.  Back to cited text no. 2
    
3.
Mahore A, Dange N, Nama S, Goel A. Facio-auriculo-vertebro-cephalic spectrum of Goldenhar syndrome. Neurol India 2010;58:141-4.  Back to cited text no. 3
[PUBMED]  [Full text]  
4.
McKenzie J. The first arch syndrome. Arch Dis Child 1958;33:477-86.  Back to cited text no. 4
    
5.
Gibson JN, Sillence DO, Taylor TK. Abnormalities of the spine in Goldenhar's syndrome. J Pediatr Orthop 1996;16:344-9.  Back to cited text no. 5
    
6.
Scholtz AW, Fish JH 3rd, Kammen-Jolly K, Ichiki H, Hussl B, Kreczy A, et al. Goldenhar's syndrome: Congenital hearing deficit of conductive or sensorineural origin? Temporal bone histopathologic study. Otol Neurotol 2001;22:501-5.  Back to cited text no. 6
    
7.
Kumar A, Friedman JM, Taylor GP, Patterson MW. Pattern of cardiac malformation in oculoauriculovertebral spectrum. Am J Med Genet 1993;46:423-6.  Back to cited text no. 7
    


    Figures

  [Figure 1], [Figure 2], [Figure 3]



 

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