Topographical Evaluation of Penile Lichen Sclerosus Reveals a Lymphocytic Depleted Variant, Preferentially Associated With Neoplasia: A Report of 200 Cases.


Journal

International journal of surgical pathology
ISSN: 1940-2465
Titre abrégé: Int J Surg Pathol
Pays: United States
ID NLM: 9314927

Informations de publication

Date de publication:
Aug 2020
Historique:
pubmed: 24 1 2020
medline: 7 4 2021
entrez: 24 1 2020
Statut: ppublish

Résumé

Since the seminal study of Hart and Helwig in 1975, there are few detailed pathological studies of lichen sclerosus (LS). The aims of this study were to provide a detailed histopathological description of penile LS, as well as to explore its relationship with penile intraepithelial neoplasia (PeIN) or invasive carcinoma. We evaluated 200 patients and designed a topographical approach for the histological evaluation focusing in alterations of the following anatomical layers: squamous epithelium, lamina propria, dartos, and corpus spongiosum. We documented the quantity and topographical location of stromal lymphocytes. The prevalent lesions found were epithelial hyperplasia, atrophy, PeIN, basal cell vacuolization, lamina propria sclerosis, and variable patterns of lymphocytic infiltration. Various unique patterns of stromal sclerosis were described: perivascular, globular, linear, and solid fibrosis/hyalinization; any of them were found to be diagnostic for LS. The variation in the topography and density of lymphocytes was determinant for the identification of LS morphological variants: lichenoid, band-like, lymphocytic depleted, and mixed. A major finding was the identification of the variant designated as lymphocytic depleted LS, which we considered as the morphological prototype of LS associated with penile neoplasia. The detailed description of this complex lesion presented in this study may help pathologists in practice to identify and better define LS. The identification of the special variants suggests a role of the stromal lymphocytes in the process of carcinogenesis. Confirmation of the observations with more studies is necessary to determine the significance of these findings.

Identifiants

pubmed: 31969038
doi: 10.1177/1066896920901333
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

468-476

Auteurs

Adriano Piris (A)

Brigham and Women Hospital, Boston, MA, USA.
Harvard University, Cambridge, MA, USA.

Diego F Sanchez (DF)

Instituto de Patología e Investigación, Asunción, Paraguay.
Universidad Nacional de Asunción, Asunción, Paraguay.

Maria José Fernandez-Nestosa (MJ)

Instituto de Patología e Investigación, Asunción, Paraguay.
Universidad Nacional de Asunción, Asunción, Paraguay.

Sofía Cañete-Portillo (S)

Instituto de Patología e Investigación, Asunción, Paraguay.

Tania Campagnoli (T)

Instituto de Patología e Investigación, Asunción, Paraguay.

Lorena Gonzalez Stark (L)

Instituto de Patología e Investigación, Asunción, Paraguay.

Patricia Zarza (P)

Instituto de Patología e Investigación, Asunción, Paraguay.

Sabrina Oneto (S)

Instituto de Patología e Investigación, Asunción, Paraguay.

Cecilia Lezcano (C)

Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Ingrid Rodriguez (I)

Instituto de Patología e Investigación, Asunción, Paraguay.
Universidad Nacional de Asunción, Asunción, Paraguay.

Elsa F Velazquez (EF)

Miraca Life Sciences, Irving, TX, USA.
Tufts University, Boston, MA, USA.

Martin Mihm (M)

Brigham and Women Hospital, Boston, MA, USA.
Harvard University, Cambridge, MA, USA.

Antonio L Cubilla (AL)

Instituto de Patología e Investigación, Asunción, Paraguay.
Universidad Nacional de Asunción, Asunción, Paraguay.

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Classifications MeSH