A Case of Pediatric Unprovoked Deep Vein Thrombosis due to Combined Hereditary Thrombophilia of Antithrombin III and Protein S Deficiency / 임상소아혈액종양
Clinical Pediatric Hematology-Oncology
;
: 185-190, 2018.
Artículo
en Inglés
| WPRIM
| ID: wpr-717635
ABSTRACT
Unprovoked deep vein thrombosis (DVT) is uncommon in pediatric patients and, among those, combined hereditary thrombophilia is particularly rare. We present a 9-year-old Korean boy who developed lower extremity pain with swelling, and was diagnosed with unprovoked DVT due to hereditary (combined hereditary thrombophilia). Coagulation test revealed antithrombin III and protein S deficiency. The genetic work up confirmed the first case of combined antithrombin III deficiency and protein S deficiency by SERPINC1 heterozygous termination mutation [c.685C>T (p.Arg229*)] and PROS1 heterozygous missense mutation [c.1597G>A (p.Val533Met)]. He was treated with continuous heparin and catheter intervention but those were ineffective or transiently effective. His DVT gradually improved only after prolonged anticoagulation.
Texto completo:
Disponible
Índice:
WPRIM (Pacífico Occidental)
Asunto principal:
Heparina
/
Antitrombina III
/
Proteína S
/
Deficiencia de Proteína S
/
Trombofilia
/
Trombosis de la Vena
/
Deficiencia de Antitrombina III
/
Mutación Missense
/
Extremidad Inferior
/
Catéteres
Límite:
Niño
/
Humanos
/
Masculino
Idioma:
Inglés
Revista:
Clinical Pediatric Hematology-Oncology
Año:
2018
Tipo del documento:
Artículo
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