Tomezzoli Silvana, Juárez María del V, Rossi Santiago I, Lema Diego A, Barbaro Cristian R, Fiorini Sandra
Unidad 15, Clínica Quirúrgica, Hospital de Niños Dr. Ricardo Gutiérrez, Ciudad de Buenos Aires.
Arch Argent Pediatr. 2008 Jun;106(3):260-3. doi: 10.1590/S0325-00752008000300012.
Abdominal pain as an initial symptom of meningococcemia is an infrequent entity, rarely described in literature. We present a case of a 4 year-old, male, previously healthy child with a 24 hour history of fever and abdominal pain. He is admitted in a surgical unit with a diagnosis of acute abdomen for surgical resolution. The clinical course turns unfavorably, and patient presents signs of severe sepsis. Urgent laparotomy is performed, observing little brownish fluid and mesenteric adenitis. He then exhibits palpable purpuric rapidly progressive lesions in lower extremities, progressing to septic shock. Later, Neisseria meningitidis serogroup B is isolated from blood cultures. The aim of this article is drawing attention to a nontypical form of manifestation of meningococcemia, as a delayed diagnosis and treatment has an impact on morbidity and mortality among the pediatric population.
腹痛作为脑膜炎球菌血症的初始症状较为罕见,文献中鲜有描述。我们报告一例4岁男性患儿,既往健康,有24小时发热及腹痛病史。他因诊断为急腹症而入住外科病房,拟行手术治疗。临床病程恶化,患者出现严重脓毒症体征。紧急行剖腹探查术,术中见少量褐色液体及肠系膜腺炎。随后,他的下肢出现可触及的紫癜且迅速进展,进而发展为感染性休克。后来,血培养分离出B群脑膜炎奈瑟菌。本文旨在提醒注意脑膜炎球菌血症的一种非典型表现形式,因为延迟诊断和治疗会影响儿童人群的发病率和死亡率。