|Year : 2002 | Volume
| Issue : 3 | Page : 178-179
Accessory auricles with ectopic digit a new association
RR Mittal , Sugam
Department of Skin and VD, Government Medical College/Rajindra Hospital, Patiala, India
97, New Lal Bagh, Patiala - 147 001, India
A 25- year -old male had accessory auricles at birth and developed ectopic digit since 1 year. As this association could not be traced in literature, it is being reported. Ectopic digit in the present case was differentiated from supernumerary digit because of late onset at the age of 24 years, ruccurence after surgery, unilateral appearance, had origin from central depression of a well defined, round plaque on the distal inter-phalangeal joint of left thumb and had curvature simulating cutaneous horn. X-ray thumb did not reveal any bone formation in this ectopic digit.
|How to cite this article:|
Mittal R R, Sugam. Accessory auricles with ectopic digit a new association. Indian J Dermatol Venereol Leprol 2002;68:178-9
| Introduction|| |
Ear develops from branchial arches and abnormalities of first and second bronchial arch may result in accessory auricles, congenital fistulae and other external ear malformations, transmitted as autosomal dominant trait. Accessory auricle may occur alone or in combination with other abnormalities such as those of middle and inner ear and other organ systems. Ear dysplasias were reported with developmental abnormalities of genitourinary tract. CT scan was found to be more useful than MRI in the delineation of these ear anomalies.
Supernumerary digit is also an autosomal dominant developmental malformation, present from birth, often bilaterally. It arises from the surface of a normal finger, mainly on the ulnar border of the hand or near the base of the fifth digit, as a pedunculated nodule and is capped by a vestigial nail.
Congenital ectopic nail of the fifth finger has been described in literature. But ectopic digit has not been reported so far.
| Case Report|| |
A 25-year-old man presented with a single, firm to hard, 2 cm, circular, well defined plaque covered with fine scales over the distal inter-phalangeal joint of left thumb and from its central depression protruded a firm digit, which was curved, 2.25 cm in length, with overlying normal skin and distal, which was curved, 2.25 cm in length, with overlying normal skin and distal nail formation [Figure - 1]. This digit was present since 1 year and patient got it removed surgically but it recurred 1 month back and slowly progressed to attain the present size. No history of injury was elicited and family history was also not contributory. Routine investigations were normal and X-ray examination of thumb revealed no bony growth.
Patient also had associated pre-auricular anomalies present in the form of two accessory auricles. Larger one was 2 x 0.5 cm, oval, skin coloured, firm nodule present just anterior to the tragus and another smaller one 0.3 cm, round, firm nodule present just above it [Figure - 1].
| Discussion|| |
Although ear malformations have been reported to be to associate with various organ abnormalities, association with ectopic digit has not been reported.
Clinical appearance, as confirmed from the photograph, clearly revealed that the left thumb lesion was an ectopic digit and had many differences from supernumerary digit such as appeared at the age of 24 years, recurred after surgical excision, was unilateral, was present on the distal interphalangeal joint of left thumb and protruded from central depression of an abnormal plaque present at its base rather than from the normal skin. Late onset of ectopic digit could be due to stimulation of ectopic germ cells by some unknown factors. Exact explanation for association of ectopic digit and accessory auricles cannot be given.
| References|| |
|1.||Tadini G, Cambiaghi S, Scarabelli G, et al. Familial occurrence of isolated accessory tragi. Pediatr Dermatol 1993;10:26-28. |
|2.||Melnick M. The etiology of external ear malformations and its relation to abnormalities of middle ear, inner ear and other organ systems. In: Birth Defects: Original Article Series, March of Dimes Birth Defects foundation, Vol XVI. New York: Alan R Liss 1980:303-331. |
|3.||Melnick M. Hereditary hearing loss and eardysplasia-renal dysplasia syndromes: syndrome delineation and possible pathogenesis. In: Levin LS ed, Birth Defects: Original Article Series, March of Dimes Birth Defects Foundation, Vol XVI. New York: Alan R Liss 1980:59 -72. |
|4.||Muckherji SK, Tart RP, Slattery WH, et al. Evaluation of first bronchial arch anomalies by CT and MRI. J Comput Assist Tomour 1993;17:576-581. |
|5.||Chung J, Nam IW, Ahn SK, et al. Rudimentary polydactyly. J Dermatol 1994;21:54-55. |
|6.||Katayama I, Maeda M, Nishioka K. Congenital ectopic nail of the fifth finger. Br J Dermatol 1984;111:231-233. |