Gow Kenneth W, Hayes-Jordan Andrea A, Billups Catherine A, Shenep Jerry L, Hoffer Frederic A, Davidoff Andrew M, Rao Bhaskar N, Schropp Kurt P, Shochat Stephen J
Department of Surgery, St Jude Children's Research Hospital, Memphis, TN 38105-2794, USA.
J Pediatr Surg. 2003 Sep;38(9):1354-60. doi: 10.1016/s0022-3468(03)00395-6.
The aim of this study was to evaluate the outcome of children undergoing treatment for malignancy and immunodeficiency syndromes in whom invasive pulmonary aspergillosis (IPA) developed.
The authors reviewed the medical records of all patients treated at their institution from January 1990 to August 1999 for culture-proven pulmonary aspergillus infection.
Among the 43 patients studied, the median age at the time of diagnosis of IPA was 13.1 years. The most common primary diagnoses were acute myelogenous leukemia (n = 18) and acute lymphoblastic leukemia (n = 14); 27 patients (63%) had received a bone marrow transplant (BMT). Of the 18 patients who underwent surgical intervention for IPA, 14 (78%) had one operation, whereas the remaining 4 patients had 2. The 4 patients alive at the time this report was written had undergone surgical intervention 2, 10, 23, and 44 months previously respectively. Surgical resection of the involved lung parenchyma was significantly prognostic for survival (P <.001). Other factors that influenced outcome were the extent of pulmonary invasion, steroid use, and the timing of bone marrow transplantation (BMT) in regard to the diagnosis of IPA.
The overall mortality rate of children treated for malignancies and immunodeficiency syndromes in who IPA develops remains high, and antifungal therapy alone may not be curative. Surgical resection may provide a small but possibly the only chance for survival. Therefore, we would advocate for resection of all involved tissue, even if it requires reoperation.
本研究旨在评估患有恶性肿瘤和免疫缺陷综合征且发生侵袭性肺曲霉病(IPA)的儿童的治疗结果。
作者回顾了1990年1月至1999年8月在其机构接受治疗且经培养证实为肺部曲霉菌感染的所有患者的病历。
在研究的43例患者中,IPA诊断时的中位年龄为13.1岁。最常见的原发性诊断为急性髓性白血病(n = 18)和急性淋巴细胞白血病(n = 14);27例患者(63%)接受了骨髓移植(BMT)。在18例因IPA接受手术干预的患者中,14例(78%)接受了一次手术,其余4例患者接受了2次手术。在撰写本报告时存活的4例患者分别在2、10、23和44个月前接受了手术干预。受累肺实质的手术切除对生存具有显著的预后意义(P <.001)。影响预后的其他因素包括肺部侵袭程度、类固醇使用以及骨髓移植(BMT)相对于IPA诊断的时间。
患有恶性肿瘤和免疫缺陷综合征且发生IPA的儿童的总体死亡率仍然很高,仅抗真菌治疗可能无法治愈。手术切除可能提供一个小但可能是唯一的生存机会。因此,我们主张切除所有受累组织,即使需要再次手术。