Ferenz C C, Tozzi J M
Kings County Hospital, Brooklyn, New York.
Clin Orthop Relat Res. 1989 Jul(244):254-7.
A 42-year-old Factor-VIII-deficient hemophiliac developed an infected pseudocyst and subsequent clostridial sepsis. Wide surgical debridement and precise medical management provided for survival in this patient's case. The treatment of choice for this rarely encountered problem was radical excisional surgery along with antibiotics and replenishment of all necessary blood products.
一名42岁的VIII因子缺乏型血友病患者出现了感染性假性囊肿，随后发生梭菌败血症。广泛的手术清创和精确的药物治疗使该患者得以存活。针对这个罕见问题的治疗选择是根治性切除手术，同时使用抗生素并补充所有必要的血液制品。
