Transition from lichen sclerosus to squamous cell carcinoma in a single tissue section.

نویسندگان

  • Joung Soo Kim
  • Min Won Lee
  • Jun Oh Paek
  • Ho Song Kang
  • Hee Joon Yu
چکیده

E6 CUTIS WWW.CUTIS.COM To the Editor: Lichen sclerosus (LS) is a chronic inflammatory disorder of unknown etiology that most commonly affects the anogenital region. Progressive sclerosis results in scarring with distortion of the normal epithelial architecture.1,2 The lifetime risk for developing squamous cell carcinoma (SCC) as a complication of long-standing LS has been estimated as 4% to 6%.3,4 However, there is no general agreement concerning the exact relationship between anogenital LS and SCC.1 The coexistence of histologic findings of LS, vulvar intraepithelial neoplasia (VIN), and SCC in the same tissue is rare. We report a case of VIN and SCC developing in a region of preexisting LS. A 76-year-old woman presented with a 7-mm nodule on the clitoris that was surrounded by a pearly white, smooth, glistening area (Figure 1). The patient reported pain and tenderness associated with the nodule. No regional lymphadenopathy was evident. We performed an excisional biopsy of the entire nodule and a small part of the whitish patch (Figure 2A). On histologic examination, Transition From Lichen Sclerosus to Squamous Cell Carcinoma in a Single Tissue Section

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عنوان ژورنال:
  • Cutis

دوره 97 4  شماره 

صفحات  -

تاریخ انتشار 2016