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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. |