Hori Hideyuki, Sato Yoshitake, Shitara Tosiji
Department of Pediatrics, Ota Memorial Hospital, Gumma, Japan.
Pediatr Int. 2015 Apr;57(2):299-301. doi: 10.1111/ped.12417.
We report a rare case of congenital syphilis (CS) presenting as Jarisch-Herxheimer reaction (JHR) at birth. The mother (primigravida) presented in labor and had not received antenatal care. She was given prophylactic ampicillin 2 g i.v. on admission and delivered shortly thereafter. The male infant (2899 g) had normal vital signs, conjunctival congestion, splenohepatomegaly, and maculopapular rash with small blisters over the entire body. Serological tests on the infant and mother confirmed CS. The infant was given i.v. ampicillin for 14 days (50 mg/kg per day until day 3, 100 mg/kg per day thereafter). One hour after the first injection, the infant developed fever (39°C), tachycardia and tachypnea without worsening of rash. Vital signs improved gradually. The rash reduced markedly at postnatal day 1, and disappeared without pigmentation at day 3. This was considered a JHR following ampicillin injection given to the mother before delivery and to the infant after birth.
我们报告了一例罕见的先天性梅毒(CS)病例,该病例在出生时表现为赫氏反应(JHR)。母亲(初产妇)分娩时前来就诊,未接受过产前护理。入院时给予其静脉注射2克预防性氨苄西林,随后不久分娩。男婴(体重2899克)生命体征正常,有结膜充血、肝脾肿大,全身出现伴有小水泡的斑丘疹。对婴儿和母亲的血清学检测确诊为先天性梅毒。给婴儿静脉注射氨苄西林14天(第1至3天每天50毫克/千克,之后每天100毫克/千克)。首次注射后1小时,婴儿出现发热(39°C)、心动过速和呼吸急促,皮疹未加重。生命体征逐渐改善。皮疹在出生后第1天明显减轻,第3天消退且无色素沉着。这被认为是在分娩前给母亲及出生后给婴儿注射氨苄西林后发生的赫氏反应。