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Warty Dyskeratoma

Visit:  Dermpath-India

High power view showing suprabasilar clefting with numerous acantholytic and dyskeratotic cells within the lacuna. Corps ronds and grains are well developed in this skin lesion.

Warty dyskeratoma of the oral mucosa. Correlated light and electron microscopic study.Oral Surg Oral Med Oral Pathol. 1984 Aug;58(2):176-83.

A warty dyskeratoma arising from the palatal mucosa of a 36-year-old man was studied by light and electron microscopy. The ultrastructural features of this lesion were compared with those of the lesions of Darier's disease. Histologic sections showed a keratin-filled depression of the epithelial surface, suprabasal clefting, and acantholytic, dyskeratotic grains and corps ronds. Electron microscopic examination revealed a decrease in the number of intact attachment sites on the surfaces of the epithelial cells adjacent to the suprabasal cleft. Acantholytic grains within the cleft contained dense bands of tonofilaments and were devoid of attachment sites. Corps ronds within the stratum granulosum appeared as dyskeratotic vacuolated cells. Warty dyskeratomas and the lesions of Darier's disease are clinically distinct, but the acantholytic and dyskeratotic cells characteristic of both show many ultrastructural similarities.

Warty dyskeratoma of the vulva. Int J Gynecol Pathol. 1983;2(3):286-93.

Suprabasal acantholysis of the epidermis is a histopathologic common denominator of diverse conditions such as pemphigus vulgaris, benign familial pemphigus (Hailey-Hailey), transient acantholytic dermatosis (Grover's disease), some actinic keratoses and cutaneous squamous carcinomas, keratosis follicularis (Darier's disease [DD]), and warty dyskeratoma (WD). Of these, WD rarely occurs in the vulva and is indistinguishable histologically from DD. However, DD is an inherited dermatosis (autosomal dominant) consisting of multiple keratotic papules on the face, trunk, and extremities, while WD occurs as an isolated, noninherited, single keratotic nodule mainly confined to the head and neck. We had the opportunity to study three patients who presented with isolated WD in the vulva. These patients had no other skin lesions and had no family history of DD or multiple dermatologic papulonodules. Histologically, all three vulvar lesions were indistinguishable from classic head and neck WD. WD must be clinically and histologically differentiated from vulvar dysplasia, bowenoid papulosis, squamous carcinoma, condyloma, and other viral-induced squamous lesions. WD should be added to the list of recognizable vulvar squamous lesions.

 
August 2009 

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