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Acral Mycosis Fungoides With Epidermal Microvesiculation Mucinosis. [caso clínico]

Por: Riveiro Falkenbach, Erica [Instituto de Investigación i+12] | Ruano Domínguez, Yolanda [Instituto de Investigación i+12] | Garrido Ruiz, María Concepción [Anatomía Patológica] | Ortiz Romero, Pablo Luis [Dermatología Médico-Quirúrgica y Venereología] | Rodríguez Peralto, José Luis [Anatomía Patológica].
Colaborador(es): Servicio de Anatomía Patológica | Instituto de Investigación imas12 | Servicio de Dermatología Médico-Quirúrgica y Venereología.
Tipo de material: materialTypeLabelArtículoEditor: The American Journal of dermatopathology, 2015Descripción: 37(8):632-4.Recursos en línea: Solicitar documento Resumen: Mycosis fungoides (MF) is the most common type of primary cutaneous T-cell lymphoma. This entity may present with a wide spectrum of clinicopathological manifestations and mimic different dermatoses. Among its histopathological variants, spongiosis is an infrequent finding, and spongiotic microvesiculation is particularly rare. Mucinous deposition is a common event in folliculosebaceous units of folliculotropic MF but rarely described within the epidermis. Herein, we report a patient with eczematous palmoplantar lesions whereby the histological, immunohistochemical, and molecular studies confirmed to be a unique case of MF showing epidermal microvesiculation mucinosis.
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Formato Vancouver:
Riveiro Falkenbach E, Ruano Y, Garrido M, Ortiz Romero PL, Rodríguez Peralto JL. Acral Mycosis Fungoides With Epidermal Microvesiculation Mucinosis. Am J Dermatopathol. 2015 Aug;37(8):632-4.

PMID: 25051106

Contiene 7 referencias

Mycosis fungoides (MF) is the most common type of primary cutaneous T-cell lymphoma. This entity may present with a wide spectrum of clinicopathological manifestations and mimic different dermatoses. Among its histopathological variants, spongiosis is an infrequent finding, and spongiotic microvesiculation is particularly rare. Mucinous deposition is a common event in folliculosebaceous units of folliculotropic MF but rarely described within the epidermis. Herein, we report a patient with eczematous palmoplantar lesions whereby the histological, immunohistochemical, and molecular studies confirmed to be a unique case of MF showing epidermal microvesiculation mucinosis.

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