Matsubara Kousaku, Omori Koichi, Baba Kunizo
Department of Pediatrics, Nishi-Kobe Medical Center, 5-7-1 Kojidai, Nishi-Ku, 651-2273, Kobe, Japan.
Int J Pediatr Otorhinolaryngol. 2002 Jan 11;62(1):63-7. doi: 10.1016/s0165-5876(01)00597-3.
We report a 2-month-old boy with severe congenital neutropenia (SCN), who developed acute necrotizing otitis media and coalescent mastoiditis due to methicillin-sensitive Staphylococcus aureus. The infection fulminantly progressed within a day to a subtotal perforation of the tympanic membrane, destructive bony changes of ossicles, lateral subperiosteal abscess, and suppurative labyrinthitis. Despite the combined treatment with intravenous antibiotics and granulocyte colony-stimulating factor, the infection resulted in mixed hearing impairment. Much attention should be given to prompt diagnosis of otomastoiditis in SCN, a rare congenital disorder, since resultant acoustic sequelae may affect subsequent speech development and intellectual ability.
我们报告了一名患有严重先天性中性粒细胞减少症(SCN)的2个月大男婴,他因对甲氧西林敏感的金黄色葡萄球菌感染而发展为急性坏死性中耳炎和融合性乳突炎。感染在一天内迅速进展,导致鼓膜大部分穿孔、听小骨骨质破坏、外侧骨膜下脓肿和化脓性迷路炎。尽管联合使用了静脉抗生素和粒细胞集落刺激因子进行治疗,但感染仍导致了混合性听力障碍。对于SCN这种罕见的先天性疾病中的耳乳突炎,应给予及时诊断高度重视,因为由此产生的听觉后遗症可能会影响后续的语言发育和智力。