RESUMEN
The development of deep vein thrombosis in an osteoarticular infection in children is rare. We report the case of two siblings with an osteoarticular infection in the hip and in the knee, respectively, who developed deep vein thrombosis and, in one sibling, pulmonary thromboembolism. The only hematological alteration found was reduction of anti-thrombin III in both patients. This reduction was acquired and secondary to sepsis due to Staphylococcus aureus. Anti-thrombin III levels recovered after 2 weeks of treatment. The association of deep vein thrombosis and osteoarticular infection with sepsis should lead to suspicion of hematological deficiencies, including acquired anti-thrombin III deficiency.
Asunto(s)
Deficiencia de Antitrombina III/complicaciones , Enfermedades Óseas Infecciosas/etiología , Articulación de la Cadera , Articulación de la Rodilla , Infecciones Estafilocócicas/etiología , Trombosis de la Vena/etiología , Adolescente , Deficiencia de Antitrombina III/genética , Niño , Femenino , Humanos , MasculinoRESUMEN
El déficit congénico de antitrombina III (AT III) es una patología de escasa prevalencia que se manifiesta clínicamente por fenómenos tromboembólicos que ocurren principalmente en territorio venoso, especialmente de las extremidades inferiores. En estos pacientes la incidencia de trombosis venosa aumenta con la edad, al igual que al someter a los pacientes a factores disponibles como son cirugía, parto, trauma, reposo prolongado, etc. Por esta razón la terapia profiláctica-anticoagulante en estos enfermos es necesaria cuando debe someterse a una cirugía. La administración de AT III exógenal, sola o junto a heparina, aparece como el tratamiento profiláctico más efectivo en prevenir los eventos trombólicos. En el presente trabajo se describe la evolución y manejo terapéutico de una paciente portadora de un déficit congénito de AT III, en relación a su segundo parto y cirugía de terceros molares
Asunto(s)
Humanos , Femenino , Adulto , Embarazo , Deficiencia de Antitrombina III/complicaciones , Cuidados Intraoperatorios , Procedimientos Quirúrgicos Orales/métodos , Anticoagulantes/administración & dosificación , Deficiencia de Antitrombina III/congénito , Complicaciones Hematológicas del Embarazo/tratamiento farmacológico , Premedicación/métodosRESUMEN
We report 10 patients with congenital deficiencies of the natural anticoagulant proteins S, C and antithrombin III. Thirteen of a total of 30 pregnancies were managed at the perinatal branch of our department. We discuss the mechanism of action of these proteins and their role in thrombotic events. We analyze the most frequent thrombotic complications and we discuss the general guidelines for the investigation of a patient with a suspected congenital thrombophilia with special regard to its management during pregnancy, delivery and perinatal outcome.
Asunto(s)
Deficiencia de Antitrombina III/congénito , Complicaciones Cardiovasculares del Embarazo/etiología , Complicaciones Cardiovasculares del Embarazo/prevención & control , Deficiencia de Proteína C/congénito , Deficiencia de Proteína S/congénito , Trombosis/etiología , Trombosis/prevención & control , Adulto , Deficiencia de Antitrombina III/complicaciones , Femenino , Humanos , Recién Nacido , Embarazo , Deficiencia de Proteína C/complicaciones , Deficiencia de Proteína S/complicaciones , Estudios Retrospectivos , Factores de RiesgoRESUMEN
We report a 24 years old female with a Superior Mesenteric and Portal Vein Thrombosis due to an Antithrombin III factor deficiency, associated to oral contraceptive use and smoking. She presented with severe abdominal pain and the diagnosis was reached after surgery with a CT scan. The patient was treated with intravenous heparin and oral anticoagulation, with a good clinical and Doppler endo-sonographic response. One month after the onset, she developed an intestinal occlusion caused by two concentric jejunal stenoses, measuring 2 and 0.7 cm in length and demonstrated with a barium jejunogram. A 35 cm intestinal resection was done and the patient recovered uneventfully. The pathological study showed granulation tissue on both stenotic zones with an ulcer near to the distal stricture, that reached the internal muscularis propria, with subserosal fibrosis. The development of segmental stenosis is a rare complication superior mesenteric vein thrombosis, that must be bore in mind.