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Bilateral type of nevus of Ota presenting as agminated lentigines


European Journal of Dermatology. Volume 13, Number 2, 205-6, March - April 2003, Cas cliniques


Summary  

Author(s) : Hee Young KANG, Won Hyoung KANG, Department of Dermatology, Ajou University School of Medicine, 5 Wonchon-dong, Paldal-ku, Suwon 442-721, Korea.

Summary : We report a 30-year-old female patient with a history of hyperpigmented macules of the face since the age of 7 years. The clinical appearance, brown macules in multiple segmental or grouped patterns, was suggested to be agminated lentigines. However, histologic examination of the pigmented macule revealed scattered melanocytes within the dermis. We diagnosed this lesion as a bilateral type of nevus of Ota presenting as agminated lentigines. The differential diagnosis from acquired bilateral nevus of Ota-like macules was made.

Keywords : nevus of Ota, agminated lentigines

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ARTICLE

Agminated lentigines are a pigmentary disorder characterized by multiple lentigines that are grouped within an area of normal appearing skin [1]. Segmental lentiginosis, partial unilateral lentiginosis, and lentiginous mosaicism are other terms used to describe this disorder. Histologically, the pigmented macules are characterized by prominent rete ridges of the epidermis and an increase in the melanin content of the basal layer.


The patient reported here was suggested to have agminated lentigines from the clinical appearance. However, histopathological examination revealed the presence of dermal melanocytes. This report draws attention to the careful diagnosis of segmental brown pigmented lesions of the face.


Case report


A 30-year-old Korean woman had a history of hyperpigmented macules of the face since the age of 7 years. There was no family history of similar pigmented lesions. The cutaneous examination revealed multiple brown macules measuring 2 to 3 mm in diameter on the left side of face, primarily in a V1 and V2 distribution, and right cheek (Fig. 1). The lesions were grouped within an area of normal appearing skin. Ocular and mucosal involvement was not noted. This clinical appearance, brown macules in multiple segmental or grouped patterns, was suggested to be agminated lentigines. A 2 mm punch biopsy was obtained from a macule on the forehead. The histopathological examination of the pigmented macule revealed scattered melanocytes within the dermis (Fig. 2). There was no elongation of the rete ridges or increased pigmentation of the basal layer of the epidermis. These findings were against the diagnosis of agminated lentigines. The patient was diagnosed as bilateral type of nevus of Ota.


Discussion


Nevus of Ota is a dermal melanocytic disease presenting as mottled blue-black or slate-gray macules occurring in the skin innervated by the first and second branches of the trigeminal nerve [2]. It is usually unilateral but may appear bilaterally. When nevus of Ota occurs bilaterally like in our patient, it can be confused with an acquired bilateral nevus of Ota-like macules (ABNOM). ABNOM may differ from the bilateral nevus of Ota in several points [3-5]. The acquired nature with an onset in the fourth or fifth decades is one of the fundamental characteristics of the ABNOM. This condition usually does not become apparent until the second decade of life [4], while the nevus of Ota is congenital or has an onset in the teens [5]. Thus, the early age of onset (7-year-old) in our case favors the nevus of Ota. In addition, the asymmetric distribution of pigmentation in our patient argues against the diagnosis of ABNOM. This nevus shows symmetric distribution, principally in the zygomatic region [5]. Lack of ocular pigmentation in the presented case is against the diagnosis of nevus of Ota. However, abnormalities of ocular pigmentation occur in 49 % to 65 % of patients with nevus of Ota [2]. We therefore made the diagnosis of a bilateral type of nevus of Ota because of its definite asymmetric distribution and the early age of onset in our case.

CONCLUSION

This report draws attention to the careful diagnosis of segmental brown pigmented lesions of face. When the distribution of dermal melanocytes is superficial as in the present case, the nevus of Ota can be seen as having a brownish color [6]. Dermal melanocytic disease is not improved by the application of liquid nitrogen or conventional carbon dioxide laser therapy, which could be useful for lentiginosis. In our experience, selective photothermolysis with the Q-switched alexandrite laser was safe and effective for nevus of Ota [7].


Article accepted on 13/01/03

REFERENCES

1 - Micali G, Nasca MR, Innocenzi D, Lembo D. Agminated lentiginosis; a case report and review of the literature. Pediatr Dermatol 1994; 11(3): 241-5.


2 - Urabe K, Nakayama J, Hori Y, Mallory SB, Foley SA, Park YK, Hann SK, Im S. Nevus of Ota. In: Nordlund JJ, Boissy RE, Hearing VJ, King RA, Ortonne JP, eds. The pigmentary system. Oxford, 1998: 898-902.


3 - Hori Y, Kawashima M, Oohara K. Acquired, bilateral nevus of Ota-like macules. J Am Acad Dermatol 1984; 10: 961-4.


4 - Sun CC, Lu YC, Lee EF, Nakagawa H. Naevus fusco-caeruleus zygomaticus. Br J Dermatol 1987; 117: 545-53.


5 - Hidano A. Acquired, bilateral nevus of Ota-like macules J Am Acad Dermatol 1985; 12: 368-9.


6 - Hirayama T, Suzuki T. A new classification of Ota's nevus based on histopathological features. Dermatologica 1991; 183: 169-72.


7 - Kang WH, Lee ES, Choi GS. Treatment of Ota's nevus by Q-switched alexandrite laser: therapeutic outcome in relation to clinical and histopathological findings.


 

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