Department of Pediatric, Qassim University, Unizah College of Medicine and Medical Sciences, Unizah, Saudi Arabia.
Department of Pediatric, Prince Sultan Military Medical City (PSMMC), Riyadh, Saudi Arabia.
Am J Case Rep. 2022 Jun 5;23:e935971. doi: 10.12659/AJCR.935971.
BACKGROUND Invasive pulmonary aspergillosis (IPA) is the major cause of mortality and morbidity in immunocompromised patients with prolonged neutropenia and is associated with poor prognosis. Multiple factors are associated with an increased risk of invasive aspergillosis, including persistent neutropenia, impaired lymphocyte engraftment following bone marrow transplantation, cytomegalovirus disease, respiratory virus infection, cytotoxic chemotherapy, and Aspergillus colonization. Unfortunately, attempts at fungal isolation are often unsuccessful. CASE REPORT We describe a 15-year-old girl with a known case of acute myeloid leukemia (AML) with unusual cause of chest infection accompanied with a persistent radiological finding that worsened with time despite multiple levels of intervention. The optimal treatment was unclear, given that all cultures were negatives and the condition did not improve. Very interesting radiological findings will be elaborated in this case. Despite the typical radiological findings, we struggled to confirm the underlying cause of lung infection, which was demonstrated to be Aspergillus fumigatus by thoracoscopy and lavage. Eventually, when the patient started to improve, catastrophic bleeding occurred, confirming the angio-invasive nature of this organism. CONCLUSIONS IPA is still associated with very high morbidity and mortality. A high index of suspicion is needed for such cases. We recommend lavage on the third or fourth day of febrile neutropenia illness in patients who did not show clear improvement with the standard neutropenia protocol, and we suggest considering combined antifungal therapies at an earlier time point. IPA is angio-invasive and can lead to catastrophic bleeding. Earlier surgical intervention might be considered, especially in refractory localized Aspergillus.
侵袭性肺曲霉病(IPA)是中性粒细胞减少时间延长的免疫功能低下患者死亡和发病的主要原因,且预后不良。多种因素与侵袭性曲霉病的风险增加相关,包括持续中性粒细胞减少、骨髓移植后淋巴细胞植入受损、巨细胞病毒病、呼吸道病毒感染、细胞毒性化疗和曲霉菌定植。不幸的是,真菌分离的尝试往往不成功。
我们描述了一名 15 岁女孩,患有已知的急性髓细胞白血病(AML),伴有不常见的胸部感染原因,伴有持续的影像学发现,尽管进行了多次干预,病情仍随着时间恶化。由于所有培养物均为阴性且病情没有改善,因此最佳治疗方案并不明确。本病例将详细阐述非常有趣的影像学发现。尽管存在典型的影像学表现,但我们难以确认肺部感染的根本原因,通过胸腔镜和灌洗证实为烟曲霉。最终,当患者开始好转时,发生灾难性出血,证实了该病原体的血管侵袭性。
IPA 仍然与非常高的发病率和死亡率相关。对于此类病例,需要高度怀疑。我们建议在发热性中性粒细胞减少症发病的第 3 或第 4 天对未显示出标准中性粒细胞减少症方案明显改善的患者进行灌洗,如果患者病情进展,建议更早考虑联合抗真菌治疗。IPA 是血管侵袭性的,可导致灾难性出血。早期手术干预可能是必要的,特别是在难治性局部曲霉菌感染的情况下。