Rørvik Synne Dragesund, Larsen Kristoffer Stange, Helgeland Lars, Dale Håvard, Ivarsen Birgitta, Bruserud Øystein, Tvedt Tor Henrik Anderson
Department of Medicine, Haukeland University Hospital, Bergen, Norway.
Department of Medicine, Haraldsplass Deaconess Hospital, Bergen, Norway.
Case Rep Hematol. 2021 Dec 21;2021:8276937. doi: 10.1155/2021/8276937. eCollection 2021.
Necrotizing soft tissue infections are rapidly progressing infections associated with severe inflammation and cytokine release. Early recognition and surgical intervention are key factors to secure survival. The current case presents a patient with multifocal necrotizing soft tissue infection as the initial presentation of severe aplastic anaemia. . A man in his fifties was admitted with septic shock with multiorgan failure and severe pancytopenia, after two days of malaise with high fever and right flank pain. The diagnosis streptococcal necrotizing myositis was significantly delayed due to atypical clinical findings. After initial surgical exploration, the decision was made to defer from surgical debridement due to extensive involvement of several muscle groups, grave pancytopenia, and suspected dismal prognosis. Surprisingly, the patient stabilized after antibiotics and intensive care treatment. Based on severe pancytopenia and hypocellular bone marrow, with no evidence of other bone marrow disorders, the patient was diagnosed with aplastic anaemia. Treatment for aplastic anaemia with antithymocyte globulin, cyclosporine, and eltrombopaq was started, and 2 months later, a partial haematological recovery was observed. The patient could be discharged from hospital without antibiotic treatment.
This case illustrates the crucial role of a multidisciplinary approach on admission and further during the clinical course. Clinical improvement despite severe neutropenia and stabilization during immunosuppressive therapy suggest that immunological factors modulate clinical course in necrotizing soft tissue infections.
坏死性软组织感染是进展迅速的感染,与严重炎症和细胞因子释放相关。早期识别和手术干预是确保存活的关键因素。本病例介绍了一名以多灶性坏死性软组织感染为严重再生障碍性贫血首发表现的患者。一名五十多岁男性在出现两天的高热和右侧腰痛不适后,因感染性休克伴多器官功能衰竭和严重全血细胞减少入院。由于临床表现不典型,链球菌坏死性肌炎的诊断显著延迟。在初步手术探查后,由于多个肌肉群广泛受累、严重全血细胞减少以及怀疑预后不佳,决定推迟手术清创。令人惊讶的是,患者在接受抗生素和重症监护治疗后病情稳定。基于严重全血细胞减少和骨髓细胞减少,且无其他骨髓疾病证据,患者被诊断为再生障碍性贫血。开始使用抗胸腺细胞球蛋白、环孢素和艾曲泊帕治疗再生障碍性贫血,2个月后观察到部分血液学恢复。患者无需抗生素治疗即可出院。
本病例说明了多学科方法在入院时及临床过程中的关键作用。尽管存在严重中性粒细胞减少但临床症状改善以及免疫抑制治疗期间病情稳定,提示免疫因素在坏死性软组织感染中调节临床过程。