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Boletín Clínico de la Asociación Médica del Hospital Infantil del Estado de Sonora

2017, Number 1

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Bol Clin Hosp Infant Edo Son 2017; 34 (1)

Cordoma condroide presentación de un caso

Contreras AR

Language: Spanish
References: 17
Page: 55-60
PDF size: 457.12 Kb.


ABSTRACT

The chondroid chordoma is a low to intermediate level of malignancy tumor that is extremely rare in patients under 20-years. It originates from the remnants of the primitive notochord. When this tumor appears in childhood there is not certain age prevalence, even though is well known that the most common localization is coccygeal sacrum. In the following paperwork is presented a clinical case of a two years old female patient with a history of subacute flaccid paralysis that turned out to be a tumor originated in the primitive notochord, which got a favorable clinical course after the intervention of a multidisciplinary team, this case required surgical treatment and chemotherapy. Currently she has overcome successfully the surveillance stage and nowadays she is considered a complete healed patient.


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