Maxillary hemophilic pseudotumor in a patient with mild hemophilia A
Maxillary hemophilic pseudotumor in a patient with mild hemophilia A
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DOI：
10.1097/mph.0b013e3181758926
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发表时间：
2008-08-01
影响因子：
1.2
通讯作者：
Dias, Eliane Pedra
中科院分区：
文献类型：
--
作者：
Linia, Glauco Siqueira;Robaina, Tatiana Ferreira;Dias, Eliane Pedra
血友病性假瘤是罕见的，但众所周知的严重血友病A的并发症，最常见的是在股骨，胫骨，骨盆骨，髂骨，或很少在颅骨或颌骨。本报告描述了一例血友病假瘤的上颌牙槽嵴发生在一个男孩与轻度血友病A（14%因子VIII活性）。病变表现为肺泡粘膜肿胀，对眼球摘除、刮除和病灶内注射纤维蛋白胶反应良好。
Hemophilic pseudotumors are rare, but well known complications of severe hemophilia A, which most frequently develops at the femur, tibia, pelvic bones, iliac bones, or rarely in the cranium or gnathic bones. This report describes a case of hemophilic pseudotumor of the maxillary alveolar ridge that occurred in a boy with mild hemophilia A (14% factor VIII activity). The lesion, which presented as an alveolar mucosal swelling, responded well to enucleation, curettage, and intralesional fibrin glue injection.