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免疫功能低下患者镰刀菌感染的临床模式。

Clinical patterns of Fusarium infections in immunocompromised patients.

作者信息

Martino P, Gastaldi R, Raccah R, Girmenia C

机构信息

Department of Human Biopathology, University La Sapienza, Rome, Italy.

出版信息

J Infect. 1994 May;28 Suppl 1:7-15. doi: 10.1016/s0163-4453(94)95911-0.

DOI:10.1016/s0163-4453(94)95911-0
PMID:8077692
Abstract

Fusarium is an ubiquitous fungus commonly found in soil and on plants. Human infection usually occurs as a result of inoculation of the organism through the body surface, thus causing skin infection, onychomycosis, keratitis, endophthalmitis and arthritis. Dissemination may occur in subjects with underlying immunodeficiency. Among immunocompromised hosts, Fusarium sp. is an emerging pathogen in neutropenic patients. To our knowledge, since 1973, when the first disseminated fusariosis in a child with acute leukemia was reported, about 80 new cases have been reported, mainly occurring in patients with haematologic malignancies. Specific portals of entry are not well understood, nevertheless the respiratory tract, colonised gastrointestinal tract, onychomycosis, disrupted skin barrier and central venous catheter have been reported as entry sites of deep seated Fusarium infections. Fever, positive blood cultures, severe myalgias, disseminated ecthyma gangrenosum-like skin lesions, ocular symptoms and multiple-organ-system involvement are distinctive features in most cases of disseminated fusariosis. The prognosis is very poor with death generally following despite antifungal therapy, unless an increase in the white blood cell count occurs. All available antifungal drugs show a low activity against the various species of Fusarium. Nevertheless, amphotericin B seems to have the highest in vitro activity and, even if it does not appear to be effective in persistently neutropenic patients, it should be currently considered to be the treatment of choice.

摘要

镰刀菌是一种普遍存在的真菌,常见于土壤和植物上。人类感染通常是由于该生物体通过体表接种所致,从而引起皮肤感染、甲癣、角膜炎、眼内炎和关节炎。在有潜在免疫缺陷的个体中可能会发生播散。在免疫功能低下的宿主中,镰刀菌属是中性粒细胞减少患者中一种新出现的病原体。据我们所知,自1973年首次报道一名急性白血病儿童发生播散性镰刀菌病以来,已报告了约80例新病例,主要发生在血液系统恶性肿瘤患者中。具体的侵入途径尚不完全清楚,不过呼吸道、定植的胃肠道、甲癣、受损的皮肤屏障和中心静脉导管已被报告为深部镰刀菌感染的侵入部位。发热、血培养阳性、严重肌痛、播散性坏疽性脓皮病样皮肤病变、眼部症状和多器官系统受累是大多数播散性镰刀菌病病例的显著特征。预后非常差,尽管进行了抗真菌治疗,除非白细胞计数增加,否则通常会死亡。所有可用的抗真菌药物对各种镰刀菌属的活性都很低。然而,两性霉素B似乎具有最高的体外活性,即使它对持续中性粒细胞减少的患者似乎无效,但目前仍应被视为首选治疗药物。

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