Literature DB >> 34345323

Simultaneous spontaneous pneumomediastinum and pneumopericardium in a critically ill patient with COVID-19.

Mohammad Javad Behzadnia1, Abbas Samim2, Fatemeh Saboori1, Mosa Asadi3, Mohammad Javanbakht3.   

Abstract

Case in the paper is of a 24-year-old woman presenting to Baqiyatallah hospital, Tehran, Iran with the occasional fever, weakness, myalgia, fatigue, body aches, and headache who was diagnosed with Coronavirus disease-19 (COVID-19) PCR test. Chest computed tomography (CT) showed spontaneous pneumomediastinum (SPM) and pneumopericardium (SPP). Here, we described SPM, and SPP in a patient with COVID-19, presenting a severe course of the disease.
© 2021 The Authors. Published by Elsevier Inc. on behalf of University of Washington.

Entities:  

Keywords:  COVID-19; CT; Lung; Pneumomediastinum; Pneumopericardium

Year:  2021        PMID: 34345323      PMCID: PMC8321708          DOI: 10.1016/j.radcr.2021.07.062

Source DB:  PubMed          Journal:  Radiol Case Rep        ISSN: 1930-0433


Introduction

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) poses crucial health challenges for medical and public health systems worldwide [1,2]. Clinical manifestation of Coronavirus disease 2019 (COVID-19) vary from asymptomatic to severe disease [3], [4], [5], [6], [7]. Rare reports described complications such as spontaneous pneumomediastinum (SPM), and pneumopericardium (SPP), as well as pneumothorax, and subcutaneous emphysema in patients suffered from COVID-19 [8], [9], [10], [11]. We reported a rare finding of SPM and SPP complications in COVID-19 patient receiving non–invasive ventilation (NIV). Here, we presented clinical manifestation, outcome and management of a COVID-19 case with SPM, and SPP.

Case presentation

We present a case of a 24-year-old woman presenting to hospital ward with the complaint of occasional fever, myalgia, fatigue, body aches, and headache. At admission, her examination revealed a progressive dyspnea that had gradually worsened. The patient did not exhibit some of the COVID-19 infection symptoms including nausea, diarrhea, and vomiting, as well as loss of smell and taste. At the time of referral, vital signs were as follows BP: 125/70; PR: 110/Min; RR: 25/Min; O2Sat: 85% (without supplemental O2), O2Sat: 94% (by using mask); T: 37.2C (Fig. 1).
Fig. 1

First day of admission. The CT scan showed only diffused lung consolidations.

First day of admission. The CT scan showed only diffused lung consolidations. Nothing special was found in examination except for respiratory distress, tachypnea, and scattered crackles on the surface of the lungs. The patient was admitted to the hospital ward on January 26, 2021. The patient was diagnosed with COVID-19 by RT-PCR. She transferred to the ICU 42 hours after hospitalization due to severe dyspnea. Scheduled medications included dexamethasone 8 mg (twice a day), melatonin 6 mg daily, enoxaparin 6000 IU twice daily (60 mg), famotidine 40 mg twice daily, and vitamin D3 (50,000-100,000 IU/week). Reserve-bag oxygen therapy was also performed for patient. Three days later, the patient dyspnea was worsened. The pulmonary CT scan showed progression of lung lesions, presenting typical finding of COVID 19 infection (Fig. 2).
Fig. 2

CT scan of the lungs showed the progression of lung lesions and were highly recommend of COVID-19 pneumonia within 72 hours later.

CT scan of the lungs showed the progression of lung lesions and were highly recommend of COVID-19 pneumonia within 72 hours later. Therefore, the patient was administered 250 mg methylprednisolone pulse for 3 days and 2 sessions with CytoSorb were performed within the following 24 hours. She rapidly developed exacerbation of dyspnea and a decrease in oxygen saturation, requiring non–invasive ventilation (PS: 18-20, PEEP: 10-12) due to O2Sat of 70% on January 30, 2021, leading to improved O2Sat to some extent (80%). Fur fays after being on non–invasive ventilation. She developed pneumomediastinum and pneumopericardium, as well as a decrease in O2Sat (decreased from 80% to 58%). The O2Sat improved relatively with the increase of positive end expiratory pressure (PEEP) and pressure support (PS), reaching 91%. Fortunately, her echocardiography revealed no signs of cardiac tamponade (Figs. 3 A and B). Based on the symptoms, the patient alternately received NIV nasal mask. Twelve days later, achieving O2S at greater than 93% was found to improve her clinical condition. Two days later, the pulmonary CT scan revealed improvement of pneumomediastinum and pneumopericardium. During this time, medical management consisted of dexamethasone 8 mg daily, meropenem (1 g every 8 hours), Targocid 400 mg daily, 3 g/day vitamin C, ASA 80 mg daily, and atorvastatin 40 mg daily.
Fig. 3

Bilateral lung involved by Covid-19 infection, massive air is seen around the heart, and bilateral soft tissue emphysema. (A and B). Ground glass opacities combined with consolidation are seen 10 days later after the air resorption (C and D).

Bilateral lung involved by Covid-19 infection, massive air is seen around the heart, and bilateral soft tissue emphysema. (A and B). Ground glass opacities combined with consolidation are seen 10 days later after the air resorption (C and D). Following these significant findings, the NIV procedure was discontinued. Laboratory findings showed melena, hematochezia, and a decrease of hemoglobin within the following 2 days, while emergency endoscopy was found to be normal. Two days later, our patient exhibited delirium and restlessness, and psychiatric counseling was initiated due to refusing treatment. Therefore, she received haloperidol, and sertraline. At this time, nasogastric (NG) Tube was implanted for our patient, followed by gavage of medicine and food. Given worsening O2Sat level, the patient was commenced on NIV for 6 days until her mental condition returned to normal. Then, oral feeding was started and her NIV was discontinued. Seven days later, her clinical condition started improving. Her dexamethasone administration was gradually reduced and then transferred to the hospital ward. With the above treatment, her O2Sat kept improving, and patient was then discharged home along with nasal oxygen (Figs. 3 C and D). She was closely followed up and he continued having CT scan. Her last lung CT after 2 months revealed a complete resorption of air. She is now in a stable condition without any supplemental oxygen (Fig. 4).
Fig. 4

The lung CT Scan 2 month after recover at home. The lesions are resolved and there is no evidence of pnemomediastinum and pnemopericardium.

The lung CT Scan 2 month after recover at home. The lesions are resolved and there is no evidence of pnemomediastinum and pnemopericardium.

Discussion

Air leakage via diffuse alveolar damage (DAD) into the interstitium of the lung results in pneumomediastinum and its travel into the pleural or pericardial space has been described to be associated with pneumothorax and pneumopericardium [12], [13], [14]. Rare complications such as SPM, SPP, and pneumothorax have been reported in relation to COVID-19 [[8], [9], [10],15,16]. Diffuse alveolar damage has been revealed to be predominate pattern of pulmonary injury in patients suffered from COVID-19 as reported by pulmonary post-mortem findings [17]. Herein, the authors report SPM and SPP in a case of COVID-19 in association with a severe course of the disease, suggesting their association with poor prognosis, further investigations may be capable of clarifying the association of spontaneous alveolar air leakage with outcomes of COVID-19 patients, eg, poor prognosis. The presented case was a critically ill covid-19 patient with a poor outcome that survived with critical ICU care and continuous follow up. Accordingly, SPM, and SPP are rarely occurred without any positive pressure ventilation. Surprisingly, the patient started to recovery during 2 days after receiving the medical treatments without any invasive intervention. This case also showed one of the rare covid 19 complications and reasons of deterioration in such cases.

Patient consent

The authors obtained written informed consent from the patient for submission of this manuscript for publication.
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