大流行期间的多灶性肺炎

L. Ramírez, A. Mahgoub, U. Naqvi, A. Thota, J. Meharg
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引用次数: 0

摘要

在晚期黑色素瘤患者中,与细胞毒性化疗相比,免疫检查点抑制剂(icpi)已显示出实质性的优势。通过使用这些药物增强免疫反应,可能会发生与免疫相关的不良反应,通常包括皮肤毒性、肝毒性、内分泌病变,以及更罕见的肺炎。病例介绍:一名80岁的患者,既往有支气管哮喘、高血压病史,20多年前停止吸烟30年,并于2020年9月在新辅助纳沃单抗治疗下出现转移性黑色素瘤(MM),伴有5天呼吸急促加重。他否认有发热、咳嗽、胸部不适、心悸、恶心、呕吐、上腹痛、腿痛或心悸。他于2020年3月被诊断为IIIc期MM,接受了左拇切除术,并完成了5个周期的尼武单抗免疫治疗。入院时,患者窦性心动过速为115,呼吸频率为18次/分钟,血压正常,室内空气氧饱和度为80%,使用4L鼻插管后改善至94%。实验室研究表明,急性肾损伤的肌酐为1.7mg/dl(1.1基线),降钙素原低于0.05 ng/dl, d -二聚体升高至2.6mg/L,全血细胞计数和综合代谢组无显著差异。病毒血清学和痰培养结果为阴性。胸部x线显示广泛的双侧多灶空域。CTPA显示严重的弥漫性双侧空域疾病,与感染性肺炎或非感染性肺炎或肿瘤过程有关。随后,他接受了支气管镜检查,检查了RLL/LLL的BAL和RLL刷活检,结果显示恶性肿瘤和感染性病因(包括COVID-19)呈阴性。患者被诊断为3级纳武单抗引起的肺炎,并接受大剂量类固醇和经验性抗生素治疗。他的病情好转,类固醇逐渐减少,并于第13天出院。讨论:肺炎是接受纳武单抗治疗的患者中一种罕见的危及生命的并发症。当出现严重症状并需要住院治疗和补充氧气时,治疗包括停止免疫治疗剂、大剂量类固醇、预防性抗生素和如果对无反应的额外免疫抑制治疗。在全球大流行期间,多灶性肺炎的发现被推定为SARS-CoV-2,除非另有证明。尽管许多医生在COVID-19大流行期间面临着负担,但在做出诊断以进行准确治疗之前,仍要保持广泛的鉴别。
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Multifocal Pneumonia During a Pandemic
Intro: In patients with advanced melanoma, immune checkpoint inhibitors (ICPIs) have demonstrated a substantial advantage when compared to cytotoxic chemotherapies. By augmenting the immune response with these medications, immune-related adverse effects can occur, and often include dermatological toxicity, hepatotoxicity, endocrinopathies, and much more rarely, pneumonitis. Case Presentation: An 80-year-old with past medical history of bronchial asthma, hypertension, 30 pack year smoking history discontinued over 2 decades ago, and metastatic melanoma (MM) on neoadjuvant nivolumab presented to our hospital in September of 2020 with 5 days of worsening shortness of breath. He denied any fever, cough, chest discomfort, palpitation, nausea, vomiting, epigastric/abdominal pain, leg pain, or palpitations. He had been diagnosed with stage IIIc MM in March of 2020 and underwent surgical resection of his left hallux and had completed 5 cycles of immunotherapy with Nivolumab. On admission, the patient had sinus tachycardia to 115, respiratory rate of 18 bpm, normotensive, oxygen saturation 80% on room air, improved to 94% on 4L nasal cannula. Laboratory studies were remarkable for acute kidney injury with Creatinine 1.7mg/dl (1.1 baseline), procalcitonin less than 0.05 ng/dl, elevated D-Dimer to 2.6mg/L, complete blood count, and comprehensive metabolic panel unremarkable. Viral serologies and sputum cultures resulted negative. Chest x-ray demonstrated extensive multifocal bilateral airspace. CTPA revealed severe diffuse bilateral airspace disease concerning for infectious, versus noninfectious pneumonia or a neoplastic process. He subsequently underwent bronchoscopy with BAL of RLL/LLL and RLL brush biopsy, which was negative for malignancy and infectious etiologies, including COVID-19. The patient was diagnosed with grade 3 nivolumab induced pneumonitis, and treated with high dose steroids, and empiric antibiotics. His condition improved, steroids were tapered, and he was discharged on day 13. Discussion: Pneumonitis is a rare, life-threatening complication in patients being treated with nivolumab. When severe symptoms are present and hospitalization and oxygen supplementation are indicated, treatment includes discontinuation of the immunotherapy agent, high dose steroids, prophylactic antibiotics, and additional immunosuppressive therapy if no response to During the midst of a global pandemic, findings of multifocal pneumonia are presumed to be SARS-CoV-2 until proven otherwise. Despite the burden many physicians have faced amid the COVID-19 pandemic, maintaining a broad differential until the diagnosis is made for accurate treatment.
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