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八.

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作者信息

Wu Juan, Su Jimei, Ye Xiaowei, Xu Weiqun

机构信息

Dept. of Stomatology, The Children's Hospital, Zhejiang University School of Medicine, National Clinical Research Center for Child Health, Hangzhou 310052, China.

Dept. of Hematology, The Children's Hospital, Zhejiang University School of Medicine, National Clinical Research Center for Child Health, Hangzhou 310052, China.

出版信息

Hua Xi Kou Qiang Yi Xue Za Zhi. 2022 Jul 25;40(4):489-493. doi: 10.7518/hxkq.2022.04.018.

DOI:10.7518/hxkq.2022.04.018
PMID:38596968
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9396434/
Abstract

Hemophilic pseudotumor is a rare but serious complication that occurs less frequently in the jaw, and it may lead to bleed uncontrollably and even death. This paper reported a case of hemophilic pseudotumor with extensive osteo-destruction in the right mandible, treated by factor Ⅷ replacement and with no recurrence after 10 years of follow-up.

摘要

血友病性假肿瘤是一种罕见但严重的并发症，较少发生于颌骨，可导致无法控制的出血甚至死亡。本文报道1例右下颌骨发生广泛骨质破坏的血友病性假肿瘤病例，经Ⅷ因子替代治疗，随访10年无复发。

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本文引用的文献

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