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Spindle Cell Rhabdomyosacoma of Uterus: A Case Study
Korean Journal of Pathology ; : 388-391, 2013.
Artículo en Inglés | WPRIM | ID: wpr-19718
ABSTRACT
Uterine rhabdomyosarcoma (RMS) typically presents as a mixed epithelial and mesenchymal tumors. Pure RMSs of the female genital tract are uncommon. Spindle cell variant of RMS is a rare morphologic subtype of embryonal RMS and mostly occurs in the paratesticular region of children. Here, we present a case of uterine spindle cell RMS in a 76-year-old woman. The tumor, 20x15x7 cm in size, was highly necrotic and adherent to the colon and rectum. Tumor cells were mostly spindle-shaped, and isolated rhabdomyoblasts were scattered. Immunohistochemical stains for myoglobin and myo-D1 showed diffuse positivity for tumor cells. The patient died only of disease three months after diagnosis.
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Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Recto / Rabdomiosarcoma / Útero / Colon / Colorantes / Mioglobina Límite: Niño / Femenino / Humanos Idioma: Inglés Revista: Korean Journal of Pathology Año: 2013 Tipo del documento: Artículo

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Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Recto / Rabdomiosarcoma / Útero / Colon / Colorantes / Mioglobina Límite: Niño / Femenino / Humanos Idioma: Inglés Revista: Korean Journal of Pathology Año: 2013 Tipo del documento: Artículo