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Everolimus for Treatment of Pseudomyogenic Hemangioendothelioma.
Ozeki, Michio; Nozawa, Akifumi; Kanda, Kaori; Hori, Tomohiro; Nagano, Akihito; Shimada, Akira; Miyazaki, Tatsuhiko; Fukao, Toshiyuki.
Afiliación
  • Ozeki M; Departments of *Pediatrics †Orthopedic Surgery §Pathology, Graduate School of Medicine, Gifu University, Gifu ‡Department of Pediatrics, Okayama University Graduate School of Medicine, Okayama, Japan.
J Pediatr Hematol Oncol ; 39(6): e328-e331, 2017 08.
Article en En | MEDLINE | ID: mdl-28121744
ABSTRACT
Pseudomyogenic hemangioendothelioma (PMH) is a recently described vascular neoplasm that occurs most commonly in the soft tissue of the distal extremities of young adults. Metastatic PMH can be fatal and there are no effective medications. We describe a case of a 15-year-old boy with metastatic PMH, who responded to treatment with everolimus, a mammalian target of rapamycin inhibitor. Immunohistochemistry showed that mammalian target of rapamycin was expressed in PMH biopsy specimens, which may explain the reduction in PMH tumor size following treatment.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Everolimus / Hemangioendotelioma Límite: Adolescent / Humans / Male Idioma: En Revista: J Pediatr Hematol Oncol Asunto de la revista: HEMATOLOGIA / NEOPLASIAS / PEDIATRIA Año: 2017 Tipo del documento: Article País de afiliación: Japón

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Everolimus / Hemangioendotelioma Límite: Adolescent / Humans / Male Idioma: En Revista: J Pediatr Hematol Oncol Asunto de la revista: HEMATOLOGIA / NEOPLASIAS / PEDIATRIA Año: 2017 Tipo del documento: Article País de afiliación: Japón