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Órgano Oficial de la Sociedad Mexicana de Angiología y Cirugía Vascular

2015, Number 3

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Rev Mex Angiol 2015; 43 (3)

Síndrome de Gorham-Stout

Campero-Urcullo A, Córdova-Quintal P, Lecuona-Huet N, Santillán-Aguayo E

Language: Spanish
References: 12
Page: 116-120
PDF size: 179.72 Kb.


ABSTRACT

Background. Is a malformation characterized by non-neoplastic lymphoid proliferation, affecting soft tissues and bone. There may be disseminated affeccion or a progressive bone lysis by lymphocytic infiltration. It is more common in young people, and it has not been reported more than 200 cases in the world.
Objective. To present a patient with Gorham-Stout syndrome with left pelvic limb affection.
Case report. We present a 32 years old female, with gradual increase in left pelvic limb volume and deformity starting in adolescence.
Conclusion. We should consider the disease in the presence of generalized osteolysis without apparent cause, especially in children or adolescents, and after excluding other causes of osteolysis. Early detection and monitoring should be directed to find immediately its complications, to offer patients the best therapeutic and rehabilitative option as the disease progress and affect the patient in its unpredictable way.


REFERENCES

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