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Congenital cutaneous lymphadenoma.
Fernandez-Flores, Angel; Nicklaus-Wollenteit, Ina; Sathishkumar, Dharshini; Diba, Vicky; Richard, Bruce; Carr, Richard; Moss, Celia; Nagy, Anita; Ogboli, Malobi; Colmenero, Isabel.
Afiliação
  • Fernandez-Flores A; Department of Cellular Pathology, HospitalEl Bierzo, Ponferrada, Spain.
  • Nicklaus-Wollenteit I; Biomedical Investigation Institute of A Coruña, CellCOM-ST Group, A Coruña, Spain.
  • Sathishkumar D; Department of Cellular Pathology, Hospital de la Reina, Ponferrada, Spain.
  • Diba V; Histopathology Department, Birmingham Children's Hospital, Birmingham, UK.
  • Richard B; Dermatology Department, Birmingham Children's Hospital, Birmingham, UK.
  • Carr R; Dermatology Department, Birmingham Children's Hospital, Birmingham, UK.
  • Moss C; Plastic Surgery Department, Birmingham Children's Hospital, Birmingham, UK.
  • Nagy A; Histopathology Department, Warwick Hospital, Warwick, UK.
  • Ogboli M; Dermatology Department, Birmingham Children's Hospital, Birmingham, UK.
  • Colmenero I; Histopathology Department, Birmingham Children's Hospital, Birmingham, UK.
J Cutan Pathol ; 44(11): 954-957, 2017 Nov.
Article em En | MEDLINE | ID: mdl-28796320
ABSTRACT
Cutaneous lymphadenoma is an uncommon benign neoplasm often considered to be an adamantinoid variant of trichoblastoma. Lesions present in both sexes, between 14 and 87 years of age, and are mainly located on the head and neck. Cases in children are rare and there is only 1 previous case of a congenital lymphadenoma. An 8-year-old Asian girl presented with a congenital lesion on her forehead comprising 4 pink papules, the largest 5 mm in diameter. Microscopy revealed a well-circumscribed tumor within the dermis and subcutis comprising well-demarcated epithelial lobules of basaloid and clear cells with subtle peripheral palisading, growing in a collagenous stroma but lacking retraction artefact. A relatively dense accompanying predominantly lymphocytic inflammatory cell infiltrate including both T-cells (CD3+) and B-cells (CD20+) permeated the nodules and spilled into the stroma. CD68+ histiocytes and CD1a+ Langerhans cells were moderately numerous. This is the second case of congenital lymphadenoma which-in spite of its rarity in childhood-widens the diagnostic possibilities of cutaneous lymphoepithelial tumors in children.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Cutâneas / Folículo Piloso / Doenças do Cabelo Limite: Child / Female / Humans Idioma: En Revista: J Cutan Pathol Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Espanha

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Cutâneas / Folículo Piloso / Doenças do Cabelo Limite: Child / Female / Humans Idioma: En Revista: J Cutan Pathol Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Espanha