key: cord-0796735-ufwarfzk authors: Chen, Joshua C; Wong, Darren; Rabi, Sina; Worswick, Scott; DeClerck, Brittney; Jean, Gibb title: All That Coughs Is Not Covid-19: A Delayed Diagnosis of Disseminated Coccidioidomycosis Following SARS-CoV-2 date: 2021-05-19 journal: Open Forum Infect Dis DOI: 10.1093/ofid/ofab246 sha: a079b55fa1e7b4d6ec51609419cc7fd09bd8e92f doc_id: 796735 cord_uid: ufwarfzk Coccidioides immitis (and C. posadasii) are endemic fungi of the southwestern United States and northern Mexico. Uncomplicated, symptomatic Coccidioides infection most commonly causes a self-limited pneumonia; however, immunocompromised patients can manifest severe pneumonia with an additional risk of dissemination to bone, joints, soft tissues, and in the most severe the cases, the central nervous system. In the year 2020 clinicians are challenged with a previously unseen volume of acute respiratory complaints as a result of the severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) pandemic. We present a patient with respiratory failure secondary to SARS-CoV-2 who experienced prolonged hypoxia and neurologic deterioration, eventually leading to a diagnosis of occult disseminated coccidiomycosis involving meningitis, miliary-pattern pneumonia, and cutaneous lesions. Coccidioides is a dimorphic fungus that grows in mycelial form in the laboratory and in the soil, and produces characteristic spherule structures in tissue 1 . Arthroconidia sprouting from mycelial structures in the soil travel on hot, dusty summer winds until they are inhaled by human hosts 1, 2 . The majority of Coccidioides infections are subclinical and thus never come to medical attention; however, viable organism may remain as latent granulomas. When symptoms do occur, they are most often indolent and result in respiratory symptoms persisting for weeks to months. Less than 1% of cases progress to disseminated extrapulmonary disease. Patients with immune compromising conditions such as diabetes, human immunodeficiency virus (HIV), pregnancy, solid organ transplant, and exogeneous immune suppression (inclusive of long-term corticosteroid use) have an increased risk of reactivation and disseminated disease 2, 3 . Disseminated coccidioidomycosis has an estimated mortality of 50% when occurring in these high risk patient populations 3 . The novel severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) has resulted in a global pandemic and delivered a devastating burden of disease to the United States 4 . We present a case of acute SARS-CoV-2 which was treated with dexamethasone, subsequently precipitating the rapid development of disseminated Coccidioides disease. We hypothesize that as the SARS-CoV-2 pandemic continues, additional cases of reactivation of undiagnosed coinfections are likely to be unmasked. An underappreciated role for clinicians in the management of SARS-CoV-2, particularly with increasing utilization of immunomodulator therapies, will be risk stratification of patients in order to appropriately screen for latent disease conditions and guide rapid diagnostics in the case of reactivated disease. A 65-year-old male born in Mexico with a history of poorly controlled insulin-dependent diabetes was diagnosed with severe acute respiratory distress syndrome coronavirus-2 (SARS-CoV-2) at an outpatient clinic in Los Angeles in July 2020. At the time of this diagnosis, he was without hypoxia and received instructions to self-monitor at home. Over the next 7 days he developed progressive shortness of breath and presented to the emergency department with temperature 36.9 degrees Celsius (C), heart rate of 76, blood pressure 144/91 mmHg, respiratory rate 25 breaths/minute, an oxygen saturation of 70%. On physical exam he was awake, tachypneic, with decreased breath sounds bilaterally. Chest radiography showed diffuse, bilateral, patchy A c c e p t e d M a n u s c r i p t infiltrates. Laboratory studies were remarkable for mild lymphopenia (absolute lymphocyte count 1,000 cells/mm 3 ) . No fungal diagnostics were obtained. After 5 days of hospitalization, he was discharged in stable condition, afebrile with home oxygen at 2 liters per minute and prescription for dexamethasone 6 mg daily to complete a duration of 9 days. Three weeks later he developed fever to 38.3 C and continued to complain of shortness of breath while still requiring home oxygen at 2 liters per minute. Computed tomography (CT) of the chest demonstrated diffuse, nodular, ground-glass and consolidative air space opacities with interlobular septal thickening (Figure 1 ). Mediastinal and bilateral hilar lymphadenopathy was also noted. The radiographic findings were attributed to SARS-CoV-2 despite a negative nasopharyngeal polymerase chain reaction (PCR) at this time. The patient was hospitalized for 19 days and was treated with broad spectrum antibiotics for suspected post-viral bacterial pneumonia. Expectorated sputum testing for Mycobacterium tuberculosis (MTB) was negative by PCR as well as acid-fast smear and culture. No fungal serologic testing was obtained. The patient was again discharged on home oxygen. Ten days after discharge, the patient returned by ambulance due to altered mental status, recurrent fever, and continued hypoxia. At the time of presentation, the patient had a leukocytosis 18.6 x 10 3 leukocytes with neutrophil predominance of 87.2%. Additional pertinent laboratory studies included a D-dimer of 6.66 mcg/mL and procalcitonin of 0.7 ng/mL. Repeat MTB PCR testing was again negative on 2 expectorated sputum samples. Repeat CT of the chest with pulmonary angiography showed increase in bilateral ground-glass opacities and a miliary pattern with innumerable pulmonary nodules ( Figure 2 ). Despite maximal supportive care and treatment with broad spectrum antimicrobials the patient required intubation. Dexamethasone 6mg IV daily was added on hospital day 7, at the same time infectious disease consultation was sought. Due to altered mental status and persistent fevers a lumbar puncture was performed with an opening pressure of 13 mmH 2 O, 21 nucleated cells (72% neutrophils, 24% lymphocytes, 4% monocytes), glucose 39 mg/dL, protein 70 mg/dL, and 5 red blood cells. Serum beta-D-glucan returned > 500 pg/mL. Empiric IV liposomal amphotericin B was initiated. On hospital day 16, the patient developed 1-3mm, round, discrete, pink, purpuric macules along the anterior and posterior lower extremities. (Figure 3) . Two punch biopsy specimens of the skin were obtained for histologic examination and tissue culture. The patient's mental and respiratory status rapidly deteriorated and after discussion with his family, his care transitioned to prioritize comfort-oriented goals. Posthumously, tissue cultures from his punch biopsies isolated Coccidioides immitis and Candida albicans. Tissue histology revealed mixed inflammation in the upper dermis with many spherules morphologically consistent with coccidioidomycosis (Figure 4) . Cerebrospinal fluid Coccidioides A c c e p t e d M a n u s c r i p t antibody complement fixation titers returned at 1:16, and a serum Coccidioides antigen returned at greater than the upper limit of detection. Each year in respiratory virus season (historically spanning November to April when influenza and respiratory syncytial virus undergo widespread community transmission) pneumonia secondary to Coccidioides competes for recognition 5 . The emergence of SARS-CoV-2 creates a new respiratory virus timeline, prompting clinicians to consider it in the differential diagnosis of patients with respiratory symptoms regardless of location or season 4 . Clinician awareness is essential for the diagnosis of invasive Coccidioides disease and the increasing reported prevalence over the past 5 years suggests that awareness is improving 6 . Since 2015, 11,000 -15,000 cases of invasive Coccidioidal disease have been reported annually; the true prevalence is likely underestimated as many are asymptomatic 6 . Superimposed infection, acute coinfection of pulmonary Coccidioides and SARS-CoV-2, and disseminated Coccidioides temporally related to acute SARS-CoV-2 have all been reported 7-9 . In areas where Coccidioides is endemic, and in non-endemic areas for patients with prior exposure, the overlapping signs and symptoms of severe acute or reactivated Coccidioides pneumonia and viral pneumonia include fever, shortness of breath, cough, and hypoxia 2, 10 . Due to this overlap in clinical presentations, symptoms of severe pulmonary Coccidioidomycosis may be attributed to severe viral pneumonia when SARS-CoV-2 testing is positive. Our case highlights the challenge facing providers in the era of pandemic SARS-CoV-2 to distinguish respiratory complaints due to acute viral pneumonia and those of underlying more chronic pulmonary disease. As patients delay presentation for chronic symptoms in the context of the ongoing pandemic, concurrent SARS-CoV-2 may become the "tipping point" for patients to seek care 11 . In our case the history of SARS-CoV-2 served as a distractor from his progressive fungal disease as concern for persistent viral pneumonia prevailed; the progressive reticulonodular infiltrates on imaging and his protracted hypoxia, though atypical for a viral pneumonia, failed to alert providers to an alternative disease process. Patients may experience prolonged shortness of breath and cough following acute SARS-CoV-2; clinicians may distinguish patients who require further investigation by the presence of relevant comorbid conditions, which include poorly controlled diabetes, HIV, malignancy, exogeneous immune suppression, and the presence of radiographic findings inconsistent with resolving viral pneumonia 12 . Short-term glucocorticoids, such as the standard 10-day course of dexamethasone A c c e p t e d M a n u s c r i p t used to treat severe SARS-CoV-2 disease, are not typically regarded as deleterious in Coccidioides disease, but without concurrent antifungal therapy the inhibited T-cell function and associated hyperglycemia that accompanies high dose steroids may indeed worsen the disease 13, 14 . Poorly controlled diabetes, as in the case of our patient, is a well-recognized risk factor for disseminated disease; the contribution to development and progression of Coccidioides disease by his multiple exposures to high dose glucocorticoids is difficult to exclude 2, 13 . Our patient did not receive a biologic immunomodulator, but this is a significant concern as the utilization of these agents become widespread in the management of SARS-CoV-2 disease 15, 16 . When considering prolonged exogenous immune suppression in the context of SARS-CoV-2, recognition of patients at risk for reactivation and dissemination of latent diseases requires careful history taking. Patients with latent disease who develop impaired T-cell immunity, as in poorly controlled diabetes, uncontrolled HIV, recipients of cytotoxic chemotherapy, solid organ transplant recipients, or those receiving high dose corticosteroids, carry risk for reactivation and dissemination of granulomatous disease such as Coccidioides, Histoplasma, Blastomyces, and Mycobacterium tuberculosis 17, 18 . These patients can be identified by eliciting prior travel and residential history; long-term residence in areas endemic for these pathogens is generally enough to raise the suspicion for latent disease. For patients and providers in non-endemic areas, recognition of prior residency in endemic areas as a risk factor for latent Coccidioides disease is essential when considering initiation of immunosuppression. In the case of Coccidioides and Mycobacterium tuberculosis, screening tests (imperfect as they are) for latent disease are available in the form of antibody testing and the QuantiFERON-Gold assay, respectively. Imaging with evidence of calcified intra-thoracic lymph nodes, upper lobe scarring, and evidence of prior granulomatous disease are additional evidence that an individual may harbor viable, latent organisms with potential to reactivate in a setting of immune suppression. Consideration for latent disease testing, and at minimum vigilance for signs and symptoms of reactivated disease, is advisable when initiating exogenous immune suppression in these high-risk groups. Patients in these high-risk groups with protracted hypoxic respiratory failure and imaging findings with nodular infiltrates, round consolidations, or cavitating disease may require empiric treatment while diagnostics are pursued. A c c e p t e d M a n u s c r i p t In the era of the SARS-CoV-2 pandemic healthcare workers are challenged more than ever to rapidly triage and identify the cause of respiratory complaints. Distinguishing uncomplicated acute viral pneumonia from underlying chronic pulmonary disease requires attention to the duration of symptoms, epidemiologic risk for exposure to endemic pathogens with pulmonary involvement, and scrutiny of available imaging for evidence of prior exposure. Identification of patients at elevated risk for reactivation and dissemination of latent granulomatous fungal or mycobacterial disease is achieved with attention to the combination of epidemiologic risk factors and underlying impaired T-cell immunity. Patients who have this combination of risk factors may benefit from screening with serologic testing where reasonably good screening tests exist (i.e., Coccidioides and Mycobacterium tuberculosis), and clinical monitoring for signs and symptoms of reactivation otherwise. The authors have no conflicts of interest to disclose. Written informed consent was obtained from the patient's next of kin for publication of this case report and accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of this journal on request. A c c e p t e d M a n u s c r i p t This work did not receive any specific grant from funding agencies in the public, commercial, or not-for-profit sectors. The early history of coccidioidomycosis Risk Factors for Disseminated Coccidioidomycosis, United States. 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