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一名急性淋巴细胞白血病患者因侵袭性曲霉病导致硬腭穿孔。

Hard palate perforation due to invasive aspergillosis in a patient with acute lymphoblastic leukemia.

作者信息

Karabulut Aylin Bilgin, Kabakas Fatih, Berköz Omer, Karakas Zeynep, Kesim Sinan Nur

机构信息

Istanbul Medical Faculty, Department of Plastic and Reconstructive Surgery, Istanbul, Turkey.

出版信息

Int J Pediatr Otorhinolaryngol. 2005 Oct;69(10):1395-8. doi: 10.1016/j.ijporl.2005.03.035.

Abstract

Invasive aspergillosis (IA) is a major cause of morbidity and mortality in immunosuppressed patients. Primary oral invasive aspergillosis is a rare condition. We present an acute lymphoblastic leukemia (ALL) patient with hard palate perforation due to invasive aspergillosis. Two months after the appearance of the fungal lesions, perforation of the hard palate was seen despite amphotericin-b and itracanazole therapy. After debridement of necrotic tissue the patient was followed for spontaneous closure for 6 months but it was seen that the fistula persisted despite the disappearance of the infection. The patient was operated for closure of the palatal fistula and there was no recurrence in 6 months of follow up. Surgical and medical management was performed successfully. Invasive oral aspergillosis is a potentially lethal disease and it should be considered in immunosuppressed patients with oral lesions.

摘要

侵袭性曲霉病(IA)是免疫抑制患者发病和死亡的主要原因。原发性口腔侵袭性曲霉病是一种罕见疾病。我们报告一例急性淋巴细胞白血病(ALL)患者因侵袭性曲霉病导致硬腭穿孔。真菌病变出现两个月后,尽管使用了两性霉素B和伊曲康唑治疗,仍可见硬腭穿孔。在清除坏死组织后,对患者进行了6个月的随访观察其自行愈合情况,但尽管感染已消失,瘘管仍持续存在。患者接受了腭瘘闭合手术,随访6个月无复发。手术和药物治疗均取得成功。侵袭性口腔曲霉病是一种潜在致命性疾病,对于有口腔病变的免疫抑制患者应予以考虑。

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