1例伯特·霍格·杜布综合征患者的新冠肺炎并发症

A. Sunny, Varun B. Shah, T. Topacio, V. Voin
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引用次数: 0

摘要

BHD综合征是一种常染色体显性遗传病,以肺囊肿、自发性气胸、头颈部皮肤错构瘤和肾恶性肿瘤为特征。我们提出了一例BHD综合征患者继发于COVID - 19的并发症。55岁男性,以发热、寒战及左侧胸膜性胸部不适1天为临床表现。他最近因细菌性肺炎住院,大约5周前感染了新冠肺炎。几个月前,患者被诊断出患有肺大疱,正在等待择期手术切除。生命体征:血压135/91毫米汞柱,体温36.5摄氏度,心率74,呼吸率18。体检发现左下叶呼吸音减少。白细胞计数10.7 K/mcL, d -二聚体0.81 mcg/mL,乳酸0.7 mmol/L。SARS冠状病毒2 PCR阳性。胸部x线显示左下叶多分叶空洞性肿块。胸部CT血管造影显示左下叶原有的大多隔大泡内出现气液水平发展,左侧胸腔积液依赖分层(图1)。患者入院时开始使用万古霉素和哌拉西林-他唑巴坦。由于胸腔积液少,无法进行胸腔穿刺。患者在抗生素治疗和支持性护理下病情稳定,出院后给予哌拉西林-他唑巴坦治疗2周。BHD的诊断包括以下一项或多项:大于2个或2个以上的纤维滤泡瘤或毛癣,肺基底区多发双侧肺囊肿,双侧多灶性肾癌或肾嗜瘤性肿瘤,致病性FLCN基因变异或家族史[4]。这些患者的最初表现通常是自发性气胸。70%-80%的BHD患者出现大量双侧肺囊肿,多数肺功能正常或轻度阻塞性疾病[3,4]。在影像学上,这些薄壁,不规则形状的囊肿可见于肺基底区内侧。这与慢性阻塞性肺病(COPD)或原发性自发性气胸患者气胸的根尖区气泡形成对比。这名患者的独特之处在于,他最近患上了叠加细菌性肺炎的COVID - 19肺炎。患者先前已知的大疱感染随后形成脓肿。据我们所知,这是第一例伯特·霍格·杜布综合征并发肺囊肿感染和脓肿形成的病例。
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Complications of COVID 19 in a Patient with Birt Hogg Dube Syndrome
Birt Hogg Dube (BHD) syndrome is an autosomal dominant disease characterized by pulmonary cysts, spontaneous pneumothorax, skin hamartomas of the head/neck, and renal malignancies. We present a case of complications secondary to COVID 19 in a patient with BHD syndrome. A 55 year old male presented with fevers, chills and left sided pleuritic chest discomfort for 1 day. He was recently hospitalized for bacterial pneumonia and had COVID Pneumonia about 5 weeks ago. The patient was diagnosed with a lung bulla several months ago and is awaiting elective surgical resection. Vitals showed blood pressure 135/91 mmHg, temperature 36.5 Celsius, heart rate 74 and respiratory rate 18. Physical exam significant for decreased breath sounds of the left lower lobe. Labs showed white cell count 10.7 K/mcL, D-dimer 0.81 mcg/mL, lactic acid 0.7 mmol/L. SARS COV 2 PCR positive. Chest Xray showed left lower lobe multilobulated cavitary mass. CT Angiography Chest showed air-fluid level development within pre-existing large multiseptated bulla in the left lower lobe and dependently layering left pleural effusion (Figure 1). The patient was initiated on Vancomycin and Piperacillin-Tazobactam on admission. Thoracentesis was unable to be done due to low amount of pleural fluid. Patient stabilized with antibiotic treatment and supportive care, with subsequent discharge on a 2 week course of Piperacillin-Tazobactam. Diagnosis of BHD involves one or more of the following: greater than 2 or more fibrofolliculomas or trichodiscomas, multiple bilateral pulmonary cysts in the basilar lung regions, bilateral multifocal renal carcinomas or oncocytic renal tumors, pathogenic FLCN gene variant or family history of the disease [4]. Initial presentation of these patients is often via spontaneous pneumothorax. 70%-80% of BHD patients develop numerous, bilateral pulmonary cysts with majority having normal pulmonary function or mild obstructive disease [3,4]. On imaging, these thin-walled, irregularly shaped cysts are seen in the medial basilar lung regions. This is in contrast to the apical region air blebs seen in those patients with pneumothorax due to COPD or primary spontaneous pneumothorax. Our patient is unique in that he had recently developed COVID 19 Pneumonia with a superimposed bacterial pneumonia. The patient's previously known bullae became infected with subsequent abscess formation. To our knowledge, this is the first known case of Birt Hogg Dube Syndrome complicated by pulmonary cyst infection and abscess formation.
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