Disseminated Cryptococcal Disease with Diffuse Pulmonary Infiltrates in a Non-HIV Host.

M Hughes, K Trivedi, M Rudrappa
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Abstract

Introduction: We present a case of disseminated Cryptococcus in a non-HIV host, where the primary manifestation was pulmonary with diffuse pulmonary infiltrates. This patient was on high dose corticosteroids for autoimmune hemolytic anemia.

Case: A 79 year old Caucasian man with a history of autoimmune hemolytic anemia on 100 mg of prednisone daily, coronary artery disease s/p bypass surgery, ischemic cardiomyopathy, chronic obstructive pulmonary disease, sleep apnea, chronic kidney disease, and history of bilateral pulmonary emboli presented to Hematology/Oncology clinic with symptoms of productive cough, worsening shortness of breath, hemoptysis. Anticoagulation had been stopped due to symptoms. The patient was referred to the emergency department from clinic where a chest CT demonstrated numerous calcified lymph nodes and diffuses grand glass opacities worse on the right and new compared to imaging from 6 months prior. The patient was placed on empiric antibiotics for treatment of pneumonia after blood and sputum cultures were obtained. Initial blood cultures grew Cryptococcus neoformans in both sets. CSF obtained by Lumbar puncture was negative for Cryptococcal. Serum Cryptococcal antigen titer was 1:2560. Infectious disease was consulted and the patient was started on induction therapy with liposomal Amphotericin B, followed by Fluconazole consolidation therapy. Hematology/ Oncology reduced the patient's prednisone dose gradually but further complications attributed to corticosteroids eventually necessitated the need to transition to Rituximab therapy. Follow up imaging on return to pulmonary clinic demonstrated marked improvement in the bilateral infiltrates.

Discussion: This patient was unique in that he demonstrated disseminated Cryptococcus but lacked neurologic complications, which is often how disseminated disease is clinically suspected. Blood cultures resulted positive for Cryptococcus and appropriate antifungal therapy was initiated before other sites were affected. The patient was HIV negative and not a post-transplant patient but was on high dose chronic prednisone for his AIHA, and therefore immunosuppressed. Opportunistic and atypical infections should be considered in all immunosuppressed patients to aid in earlier diagnosis and prevention of further dissemination of disease and further complications.

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非hiv宿主弥漫性肺浸润的播散性隐球菌病
我们报告一例播散性隐球菌感染非hiv宿主,其主要表现为肺部弥漫性浸润。本例患者因自身免疫性溶血性贫血接受大剂量皮质类固醇治疗。病例:一名79岁白人男性,有自身免疫性溶血性贫血史,每日100mg强的松,冠状动脉疾病s/p搭桥手术,缺血性心肌病,慢性阻塞性肺病,睡眠呼吸暂停,慢性肾脏疾病,双侧肺栓塞史,到血液/肿瘤诊所就诊,症状为咳咳,呼吸急促加重,咯血。因症状停用抗凝治疗。患者从诊所转至急诊科,胸部CT显示大量钙化淋巴结和弥漫性大玻璃浊影,与6个月前的影像相比,右侧更糟,而且新的。经血、痰培养后给予经验性抗生素治疗肺炎。两组患者的初始血培养均培养出新型隐球菌。腰椎穿刺脑脊液隐球菌阴性。血清隐球菌抗原滴度为1:2560。会诊感染性疾病后,患者开始用两性霉素B脂质体诱导治疗,随后用氟康唑巩固治疗。血液学/肿瘤学逐渐减少患者的泼尼松剂量,但由于皮质类固醇引起的进一步并发症最终需要过渡到利妥昔单抗治疗。返回肺部诊所的随访影像显示双侧浸润明显改善。讨论:该患者的独特之处在于他表现出播散性隐球菌,但没有神经系统并发症,这通常是临床上怀疑播散性疾病的原因。血液培养结果隐球菌阳性,在其他部位受到影响之前开始适当的抗真菌治疗。该患者为HIV阴性,并非移植后患者,但因其AIHA而接受大剂量慢性强的松治疗,因此免疫抑制。在所有免疫抑制患者中应考虑机会性和非典型感染,以帮助早期诊断和预防疾病的进一步传播和进一步并发症。
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Where are we going? Refractory anemia. Urinary diversion. Schneiderian papilloma. Recurrent respiratory papillomatosis.
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