Genitogluteal porokeratosis - Case report*

نویسندگان

  • Flávia Regina Ferreira
  • Priscila Pacheco Lessa
  • Marcia Lanzoni de Alvarenga
چکیده

We report the case of a patient diagnosed with genitogluteal porokeratosis, a disorder of epidermal keratinization. The location described is extremely rare and very often late diagnosed or even misdiagnosed. Histopathology showed a typical cornoid lamella of great value to support this diagnosis. The importance of awareness of this entity by the specialist is emphasized as a differential diagnosis among genital diseases of chronic evolution and difficult treatment.

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Association of Porokeratosis, Vitiligo, Lichen Sclerosus et Atrophicus and Lichen Planus: A case report

Although lichen planus and vitiligo are common skin disorders, their association with two other uncommon diseases, i.e. lichen sclerosus et atrophicus and disseminated superficial actinic porokeratosis, seems to be a very rare occurrence. We report herein a 70-year-old man who developed all of these four skin disorders simultaneously.

متن کامل

Verrucous porokeratosis: A case report

Porokeratoses are uncommon hereditary or acquired keratinization disorders due to abnormal clones of keratinocytes in the epidermis. Porokeratoses have several clinical features which may occur simultaneously. A rare type is verrucous porokeratosis (VPK). Herein, we present a 47-year-old man with a 4-year history of perianal verrucous lesions and one year history of annular pruritic lesions on ...

متن کامل

Genital Porokeratosis: A Case Report of Rarely Involved Sites

Genital porokeratosis is a rare form of porokeratosis which can occur in two ways : in isolated form or as a part of disseminated porokeratosis. The former one is much rarer and less than 50 such cases of isolated involvement of genitalia in porokeratosis has been reported so far. Being a inherited disorder of keratinization, usual mode of heritance is autosomal dominant. The aim of present rep...

متن کامل

Unilateral punctate porokeratosis - Case report*

This case report involves a 20-year-old man with unilateral punctate porokeratosis. The patient presented an 8-year history of numerous asymptomatic keratotic papules and pits with linear distribution on his left pal-mar surface and fifth finger of the left hand. Histopathological examination of the keratotic plug revealed findings of distinct epidermal depressions containing cornoid lamellae. ...

متن کامل

A Case of Linear Porokeratosis: Dermoscopic and Immunofluorescence Findings

Observations: Porokeratosis is a dyskeratotic disorder of the skin characterized by hyperkeratotic papule or plaque with an annular appearance and usually diagnosed easily, both histopathologically and clinically. We present a case of linear porokeratosis which was most likely suggesting the linear epidermal nevus and linear lichen planus. We observed a tiny brown border in the dermoscopic exam...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:

دوره 88  شماره 

صفحات  -

تاریخ انتشار 2013