Teijido John, Drendel Amy L
Medical College of Wisconsin, Milwaukee, Wisconsin.
Medical College of Wisconsin, Milwaukee, Wisconsin; Children's Hospital of Wisconsin, Milwaukee, Wisconsin.
J Emerg Med. 2019 Mar;56(3):e23-e26. doi: 10.1016/j.jemermed.2018.12.035. Epub 2019 Jan 25.
Blastomycosis is caused by a fungus endemic to states and providences bordering the Lawrence Rivers and the Great Lakes. It can lead to significant pathology in both immunocompetent and immunocompromised hosts. This case report describes disseminated blastomycosis in an otherwise healthy 16-year-old patient.
A 16-year-old male presented with a chief complaint of flank pain. In the Emergency Department he described additional symptoms of emesis, cough, and weight loss. His vitals were appropriate; however, he had absent lung sounds in the left lower lung field, splenomegaly, a left thigh abscess, and lower-extremity edema. Imaging studies showed a left pleural effusion, mediastinal shift to the right, splenomegaly, a left psoas abscess, and undifferentiated bony involvement of L1 transverse process and the left 12th rib. Abscess cultures grew Blastomyces dermatitides. He was treated with amphotericin B, demonstrated clinical improvement, and was discharged on itraconazole. WHY SHOULD AN EMERGENCY PHYSICIAN BE AWARE OF THIS?: The case fatality rate of blastomycosis is estimated at between 4.3% and 6.4%. Patients with solid organ transplant and associated immune suppression had a mortality of 33-38%. Given the nonspecific nature of this condition, a high level of suspicion is required for diagnosis, and early diagnosis is essential, as end organ damage in disseminated disease can include high-severity illness, including acute respiratory distress syndrome and central nervous system dysfunction. If any patient presents with symptomatology involving both skin and pulmonary systems, blastomycosis must be entertained as a possible diagnosis. Prompt diagnosis and treatment will significantly improve morbidity and mortality.
芽生菌病由一种真菌引起,这种真菌在与劳伦斯河和五大湖接壤的州和省份呈地方性流行。它可在免疫功能正常和免疫功能低下的宿主中导致严重病变。本病例报告描述了一名原本健康的16岁患者的播散性芽生菌病。
一名16岁男性因侧腹痛为主诉就诊。在急诊科,他描述了呕吐、咳嗽和体重减轻等其他症状。他的生命体征正常;然而,他左下肺野呼吸音消失,脾肿大,左大腿有脓肿,下肢水肿。影像学检查显示左侧胸腔积液,纵隔向右移位,脾肿大,左腰大肌脓肿,L1横突和左第12肋有未分化的骨质受累。脓肿培养物培养出皮炎芽生菌。他接受了两性霉素B治疗,临床症状改善,出院时服用伊曲康唑。急诊科医生为何应了解此病?:芽生菌病的病死率估计在4.3%至6.4%之间。实体器官移植及相关免疫抑制患者的死亡率为33% - 38%。鉴于此病的非特异性,诊断需要高度怀疑,早期诊断至关重要,因为播散性疾病的终末器官损害可包括严重疾病,如急性呼吸窘迫综合征和中枢神经系统功能障碍。如果任何患者出现涉及皮肤和肺部系统的症状,必须考虑芽生菌病作为可能的诊断。及时诊断和治疗将显著改善发病率和死亡率。