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        "resumen" => "<span id="abst0005" class="elsevierStyleSection elsevierViewall"><p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">Se presenta un caso de plasmocitoma &#243;seo solitario&#44; originado en el primer arco costal izquierdo en un paciente var&#243;n de 45 a&#241;os de edad&#44; que se inici&#243; como un s&#237;ndrome de Horner&#46; La radiograf&#237;a del t&#243;rax&#44; la gammagraf&#237;a&#44; la TAC y la arteriograf&#237;a mostraron una sombra de car&#225;cter tumoral en la pared costal izquierda&#46; Los estudios cl&#237;nicos y anal&#237;ticos de la extensi&#243;n no pusieron de manifiesto la existencia de enfermedad en ning&#250;n otro nivel&#46; El tratamiento consisti&#243; en la ex&#233;resis quir&#250;rgica y radioterapia postoperatoria&#46; El estudio histol&#243;gico de la tumoraci&#243;n fue compatible con un plasmocitoma costal&#46; Actualmente&#44; 2 a&#241;os despu&#233;s&#44; el paciente se encuentra asintom&#225;tico&#44; libre de recidiva y sin evidencia de enfermedad generalizada&#46;</p></span>"
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Journal Information
Vol. 30. Issue 8.
Pages 410-413 (October 1994)
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Vol. 30. Issue 8.
Pages 410-413 (October 1994)
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Síndrome de Horner asociado a plasmocitoma óseo solitario del primer arco costal
Horner's syndrome associated with solitary bone plasmacytoma in the first rib
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J.J. Carvajal Balaguera1
Servicio de Cirugía General. Hospital Universitario de Getafe. Madrid
S. Mallagray Casas*, A. Dancausa Monge**, J.J. Canto Romero***
* Departamento de Cirugía. Hospital Universitario de Getafe. Madrid
** Cirugía Torácica. Hospital Universitario de Getafe. Madrid
*** Servicio de Anatomía Patológica. Hospital General Cruz Roja. Madrid
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Se presenta un caso de plasmocitoma óseo solitario, originado en el primer arco costal izquierdo en un paciente varón de 45 años de edad, que se inició como un síndrome de Horner. La radiografía del tórax, la gammagrafía, la TAC y la arteriografía mostraron una sombra de carácter tumoral en la pared costal izquierda. Los estudios clínicos y analíticos de la extensión no pusieron de manifiesto la existencia de enfermedad en ningún otro nivel. El tratamiento consistió en la exéresis quirúrgica y radioterapia postoperatoria. El estudio histológico de la tumoración fue compatible con un plasmocitoma costal. Actualmente, 2 años después, el paciente se encuentra asintomático, libre de recidiva y sin evidencia de enfermedad generalizada.

A case of solitary plasmacytoma originated in the left first rib in a 45 year male is presented. The initial sintomatology was a Horner's syndrome. A chest X-ray, gammagraphy, TAC and arteriography showed a tumor shadow in the left chest wall; no evidence of plasmacytoma after clinical study found use where. The treatment was surgical excision and postsurgical radiotherapy. The histological investigation revealed a plasmacytoma of the rib. The patient have been followed for two years. The patient is asymptomatic, without evidence of local recurrence and systemic spread of the disease two years after treatment.

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