RESUMEN
ABSTRACT: The presence of neoplastic melanocytes within the eccrine apparatus into the reticular dermis and/or subcutaneous tissue is extremely rare. The staging of syringotropic melanomas and their biological behavior are still controversial. We present 6 new cases of syringotropic melanoma and their main histopathologic features; review the previous literature; and discuss about the origin, staging, and prognosis of this rare variant of melanoma.
Asunto(s)
Melanocitos/patología , Melanoma/patología , Neoplasias Cutáneas/patología , Glándulas Sudoríparas/patología , Anciano , Anciano de 80 o más Años , Biomarcadores de Tumor/análisis , Biopsia , Diagnóstico Diferencial , Femenino , Humanos , Inmunohistoquímica , Masculino , Melanocitos/química , Melanoma/química , Melanoma/cirugía , Persona de Mediana Edad , Valor Predictivo de las Pruebas , Neoplasias Cutáneas/química , Neoplasias Cutáneas/cirugía , Glándulas Sudoríparas/química , Glándulas Sudoríparas/cirugía , Resultado del TratamientoRESUMEN
Toker cells (TCs) are sometimes present in the nipple epidermis as oval cells with pale cytoplasm and roundish nuclei. In most cases, TCs may be easily distinguished from cancerous cells of Paget disease of the nipple (PCs). Especially in TC hyperplasia, in which mild-to-moderate atypia may be present, it may be challenging to distinguish between TCs and PCs. The combination of chronic inflammatory changes in the nipple, in the context of Zuska disease, and TC hyperplasia, may easily lead to an erroneous diagnosis of mammary Paget disease.
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Absceso/diagnóstico , Absceso/patología , Enfermedades de la Mama/diagnóstico , Enfermedades de la Mama/patología , Fístula/diagnóstico , Fístula/patología , Pezones/patología , Adulto , Neoplasias de la Mama/patología , Diagnóstico Diferencial , Femenino , Humanos , Hiperplasia/diagnóstico , Hiperplasia/patología , Enfermedad de Paget Mamaria/patología , Fumar/efectos adversosAsunto(s)
Eosinofilia/diagnóstico , Exantema/diagnóstico , Leucemia Mieloide Aguda/complicaciones , Síndromes Paraneoplásicos/diagnóstico , Prurito/diagnóstico , Administración Cutánea , Administración Oral , Biopsia , Eosinofilia/tratamiento farmacológico , Eosinofilia/inmunología , Eosinofilia/patología , Exantema/tratamiento farmacológico , Exantema/inmunología , Exantema/patología , Femenino , Glucocorticoides/administración & dosificación , Humanos , Leucemia Mieloide Aguda/inmunología , Persona de Mediana Edad , Síndromes Paraneoplásicos/tratamiento farmacológico , Síndromes Paraneoplásicos/inmunología , Síndromes Paraneoplásicos/patología , Prurito/tratamiento farmacológico , Prurito/inmunología , Prurito/patología , Piel/inmunología , Piel/patología , Resultado del TratamientoRESUMEN
BACKGROUND: Non-neural granular cell tumor (NNGCT) is an uncommon neoplasm of controversial histogenesis and its histopathologic differential diagnosis includes, in addition to conventional GCT, other dermal tumors that may exhibit granular cell change. METHODS: Three patients with a diagnosis of NNGCT were identified in the authors' files. Hematoxylin and eosin-stained sections and immunohistochemical studies were performed. RESULTS: Histopathological study of the three lesions showed dermal proliferation of granular cells arranged in thick fascicles between collagen bundles. The lesions showed positivity for Factor XIIIa, CD163, CD68, NKIC3, vimentin, ALK, fascin, and cyclin D1. CONCLUSION: To our knowledge, positivity for cyclin D1 has not been reported to date in NNGCT. In borderline cases, where the diagnosis is unclear despite histopathologic and immunohistochemical findings, positivity for cyclin D1 may favor the diagnosis of NNGCT. Further investigations to assess the differentiation of this rare neoplasm are needed.