Mohd-Razali S, Ahmad-Affandi K, Ibrahim S, Abdul-Rashid A H, Abdul-Shukor N
Department of Orthopaedics and Traumatology, Universiti Kebangsaan Malaysia, Kuala Lumpur, Malaysia.
Department of Pathology, Universiti Kebangsaan Malaysia, Kuala Lumpur, Malaysia.
Malays Orthop J. 2023 Mar;17(1):180-183. doi: 10.5704/MOJ.2303.021.
Purpura fulminans (PF) is a severe clinical manifestation of infection that is associated with high mortality rates in children. Survivors are frequently left with debilitating musculoskeletal sequelae. There is a paucity of reports on the musculoskeletal pathology of purpura fulminans. We report on a 2-year-old boy with purpura fulminans due to meningococcemia. The child developed distal gangrene in both the upper and lower limbs. Amputations were done for both lower limbs. Histological examination of the amputated specimens showed an inflammatory process and features of osteonecrosis. The latest follow-up at the age of 6 years showed a right knee valgus due to asymmetrical growth arrest of the proximal tibia. PF and its complications are challenging to treat and may require a multidisciplinary approach to improve patient's functional ability.
暴发性紫癜(PF)是一种严重的感染临床表现,与儿童的高死亡率相关。幸存者常伴有使人衰弱的肌肉骨骼后遗症。关于暴发性紫癜肌肉骨骼病理学的报道很少。我们报告一例因脑膜炎球菌血症导致暴发性紫癜的2岁男孩。该患儿双上肢和双下肢均出现远端坏疽。双下肢均进行了截肢手术。对截肢标本的组织学检查显示有炎症过程和骨坏死特征。6岁时的最新随访显示,由于胫骨近端不对称生长停滞,出现右膝外翻。暴发性紫癜及其并发症治疗具有挑战性,可能需要多学科方法来提高患者的功能能力。