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Primary acquired melanosis (PAM) without atypia/WHO low-grade conjunctival melanocytic intraepithelial lesion over areas of oculodermal melanocytosis.
Bata, Bashar M; Salvi, Sachin M; Mudhar, Hardeep Singh.
Afiliación
  • Bata BM; Department of Oncology and Metabolism, The University of Sheffield, Sheffield, UK bbata@hotmail.com.
  • Salvi SM; Department of Ophthalmology, Sheffield Teaching Hospitals NHS Foundation Trust, Sheffield, UK.
  • Mudhar HS; Department of Oncology and Metabolism, The University of Sheffield, Sheffield, UK.
BMJ Case Rep ; 13(10)2020 Oct 22.
Article en En | MEDLINE | ID: mdl-33093059
An elderly white man with a history of left oculodermal melanocytosis presented with new onset brown pigmentation of the left bulbar and inferior tarsal conjunctiva. The bulbar conjunctival pigmentation was at the level of the conjunctival epithelium and was overlying areas of typical slate-grey scleral pigmentation characteristic of oculodermal melanocytosis. Both areas of new pigmentation were biopsied. The bulbar conjunctiva revealed primary acquired melanosis (PAM) without atypia with increased melanin production and the tarsal conjunctival biopsy showed PAM without atypia sine pigmentio overlying areas of substantia propria spindle-shaped heavily pigmented melanocytes of oculodermal melanocytosis. The case report examines the relationship between the epithelial and substantia propria melanocytes and correlates the findings with what is known about this association from the dermatopathology literature.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neoplasias Cutáneas / Nevo de Ota / Neoplasias de la Conjuntiva / Melanosis Límite: Aged80 / Humans / Male Idioma: En Revista: BMJ Case Rep Año: 2020 Tipo del documento: Article Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neoplasias Cutáneas / Nevo de Ota / Neoplasias de la Conjuntiva / Melanosis Límite: Aged80 / Humans / Male Idioma: En Revista: BMJ Case Rep Año: 2020 Tipo del documento: Article Pais de publicación: Reino Unido