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新生儿坏死性筋膜炎:三例报告及文献复习

Neonatal necrotizing fasciitis: a report of three cases and review of the literature.

作者信息

Hsieh W S, Yang P H, Chao H C, Lai J Y

机构信息

Chang Gung Children's Hospital and Chang Gung University, Taiwan, Republic of China.

出版信息

Pediatrics. 1999 Apr;103(4):e53. doi: 10.1542/peds.103.4.e53.

Abstract

OBJECTIVE

Necrotizing fasciitis (NF) is a predominantly adult disorder, with bacterial infection of the soft tissue. In children, it is relatively rare and has a fulminant course with a high mortality rate. In the neonate, most cases of NF are attributable to secondary infection of omphalitis, balanitis, mammitis, postoperative complications, and fetal monitoring. The objective of this communication is to report 3 cases of neonatal NF and provide a literature review of this disorder.

RESULTS

This review yielded 66 cases of neonatal NF. Only 3 cases were premature. There was no sex predilection and the condition rarely recurred. Several underlying conditions were identified that might have contributed to the development of neonatal NF. These included omphalitis in 47, mammitis in 5, balanitis in 4, fetal scalp monitoring in 2, necrotizing enterocolitis, immunodeficiency, bullous impetigo, and maternal mastitis in 1 patient each. The most common site of the initial involvement was the abdominal wall (n = 53), followed by the thorax (n = 7), back (n = 2), scalp (n = 2), and extremity (n = 2). The initial skin presentation ranged from minimal rash to erythema, edema, induration or cellulitis. The lesions subsequently spread rapidly. The overlying skin might later develop a violaceous discoloration, peau d'orange appearance, bullae, or necrosis. Crepitus was uncommon. Fever and tachycardia were frequent but not uniformly present. The leukocyte count of the peripheral blood was usually elevated with a shift to the left. Thrombocytopenia was noted in half of the cases. Hypocalcemia was rarely reported. Of the 53 wound cultures available for bacteriologic evaluation, 39 were polymicrobial, 13 were monomicrobial, and 1 was sterile. Blood culture was positive in only 20 cases (50%). Treatment modalities included the use of antibiotics, supportive care, surgical debridement, and drainage of the affected fascial planes. Two of the 6 cases who received hyperbaric oxygen therapy died. The overall mortality rate was 59% (39/66). In 12 cases, skin grafting was required because of poor granulation formation or large postoperative skin defects among the survivors.

CONCLUSION

Neonatal NF is an uncommon but often fatal bacterial infection of the skin, subcutaneous fat, superficial fascia, and deep fascia. It is characterized by marked tissue edema, rapid spread of inflammation, and signs of systemic toxicity. The wound cultures are predominantly polymicrobial and the location of initial involvement depends on the underlying etiologic factor. High index of suspicion, prompt aggressive surgery, appropriate antibiotics, and supportive care are the mainstays of management in the newborn infant with NF.

摘要

目的

坏死性筋膜炎(NF)主要是一种成人疾病,为软组织的细菌感染。在儿童中相对少见,病情发展迅猛,死亡率高。在新生儿中,大多数NF病例归因于脐炎、龟头炎、乳腺炎、术后并发症及胎儿监护的继发感染。本文旨在报告3例新生儿NF病例并对该疾病进行文献综述。

结果

本综述共纳入66例新生儿NF病例。仅3例为早产儿。无性别倾向,且该病很少复发。确定了几种可能促使新生儿NF发生的潜在疾病。其中脐炎47例,乳腺炎5例,龟头炎4例,胎儿头皮监护2例,坏死性小肠结肠炎、免疫缺陷、大疱性脓疱疮及产妇乳腺炎各1例。最初受累的最常见部位是腹壁(n = 53),其次是胸部(n = 7)、背部(n = 2)、头皮(n = 2)及四肢(n = 2)。最初的皮肤表现从轻微皮疹到红斑、水肿、硬结或蜂窝织炎不等。随后病变迅速扩散。随后,覆盖的皮肤可能会出现紫红色变色、橘皮样外观、水疱或坏死。捻发音不常见。发热和心动过速很常见,但并非均有出现。外周血白细胞计数通常升高并伴有核左移。半数病例出现血小板减少。低钙血症很少有报道。在可用于细菌学评估的53份伤口培养物中,39份为混合菌感染,13份为单一细菌感染,1份无菌生长。血培养仅20例(50%)呈阳性。治疗方式包括使用抗生素、支持治疗、手术清创以及引流受累的筋膜平面。接受高压氧治疗的6例患者中有2例死亡。总死亡率为59%(39/66)。12例幸存者因肉芽组织形成不良或术后皮肤缺损较大而需要进行皮肤移植。

结论

新生儿NF是一种罕见但往往致命的皮肤、皮下脂肪、浅筋膜和深筋膜细菌感染。其特征为明显的组织水肿、炎症迅速扩散及全身中毒症状。伤口培养物大多为混合菌感染,最初受累部位取决于潜在病因。高度怀疑、及时积极手术、适当的抗生素及支持治疗是新生儿NF治疗的主要手段。

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