Morales P, Ros J A, Blanes M, Pérez-Enguix D, Saiz V, Santos M
Unidad de Trasplante Pulmonar, Hospital Universitario la Fe, Valencia, Spain.
Transplant Proc. 2007 Sep;39(7):2413-5. doi: 10.1016/j.transproceed.2007.07.053.
Mycobacterium abscessus infection following lung transplantation (LT) has been described in a few cases. It is characterized by a variable initial location and subsequent course in this special risk group of patients, particularly those with cystic fibrosis (CF). Herein we have presented the case of a patient subjected to LT due to CF, who 1 year after transplantation developed a subcutaneous nodule produced by M abscessus, with subsequent hematogenous spread as well as bronchial and bone marrow involvement. Antecedents prior to LT included Staphylococcus aureus colonization and sputum positivity for Aspergillus fumigatus and Scedosporium apioespermum. Treatment with ciprofloxacin and linezolid was started on the basis of the antibiogram findings. The latter antibiotic was replaced by clarithromycin for 6 months. Two years later, the patient remains asymptomatic with respiratory function parameters in the normal range. The infected patient described herein was our only case with sepsis and multisystemic spread. The important mortality among such cases reported in the literature makes early diagnosis and treatment essential.
肺移植(LT)后脓肿分枝杆菌感染已有少数病例报道。在这一特殊风险患者群体中,尤其是囊性纤维化(CF)患者,其特点是初始感染部位和后续病程各不相同。在此,我们报告了1例因CF接受LT的患者,该患者在移植后1年出现由脓肿分枝杆菌引起的皮下结节,随后发生血行播散以及支气管和骨髓受累。LT前的病史包括金黄色葡萄球菌定植以及烟曲霉和阿萨希毛孢子菌痰检阳性。根据药敏结果开始使用环丙沙星和利奈唑胺治疗。后者抗生素被克拉霉素替代,疗程6个月。两年后,患者仍无症状,呼吸功能参数在正常范围内。本文所述的感染患者是我们唯一1例发生脓毒症和多系统播散的病例。文献报道的此类病例中死亡率较高,因此早期诊断和治疗至关重要。