key: cord-0031161-hcn5lj9u
authors: Mahler, Lily; McCleskey, Brandi
title: Lymphocytic Myocarditis
date: 2021-11-05
journal: Am J Forensic Med Pathol
DOI: 10.1097/paf.0000000000000730
sha: 269fd238880accd19fed0bad41cd001b429956b8
doc_id: 31161
cord_uid: hcn5lj9u

nan

Myocarditis is an inflammatory disease of the myocardium that is an established cause of sudden death for both adult and pediatric populations alike. The clinical presentation of myocarditis varies drastically from asymptomatic to cardiogenic shock and sudden death. Myocarditis can present as nonspecific symptoms, such as shortness of breath, nausea/vomiting, and tachycardia, but it can also mimic acute coronary syndrome. 2 The clinical outcomes for myocarditis are also broad: a portion of patients have a full recovery, some require circulatory support or cardiac transplantation, and some develop long term sequelae such a dilated cardiomyopathy. The most common causes of death due to myocarditis are heart failure and dysrhythmia.

Because of the heterogeneous nature of myocarditis, diagnosis can prove difficult and the true incidence of the disease is likely to be higher than reported cases. The rate of histologically proven myocarditis in 1516 pediatric cases sent to autopsy over 10 years was higher at 2%; this cohort of patients also had a sudden death rate of 57%. 3 Given that the clinical presentations of myocarditis are heterogeneous and often overlap with other cardiac diseases, this type of case is quite challenging for both the forensic pathologist and the clinician. Outside of autopsy, the criterion standard for clinical diagnosis of myocarditis is the endomyocardial biopsy (EMB). The diagnostic power of EMB has been strengthened by using PCR in the detection of viral genomes within biopsy samples. 4 The most common etiology of myocarditis in the United States is viral infection. Commonly identified viruses implicated are enteroviruses (specifically Coxsackie B serotype), parvovirus B19, human herpesvirus 6, and adenovirus. In total, approximately 20 different cardiotropic viruses have been associated with myocarditis. 4 Other etiologies of myocarditis include bacterial infection, drug-induced hypersensitivity or toxicity, and autoimmune forms. Since late 2019, the SARS-CoV-2 has spread worldwide, and although most manifestations of the infection are respi-ratory in nature, a number of case series have been associated with severe cardiac sequalae as well. Numerous case reports have described clinical presentations of acute myocarditis in association with COVID-19. [5] [6] [7] [8] Unfortunately, few of the current case reports on COVID-19-related myocarditis have histological confirmation. According to a Journal of American College of Cardiology review in January 2021, EMB was performed in 9 cases of COVID-19-positive patients, 2 of which met diagnostic criteria for myocarditis; all 9 cases lacked evidence of SARS-CoV-2 within cardiomyocytes. 9 In a systematic review performed in September 2020 analyzing cardiac autopsy findings of COVID-19-positive decedents, few cases revealed myocarditis upon postmortem examination. 10 The majority of cardiac pathology included cardiac dilatation, ischemia, or thrombosis, whereas only 1.5% of cases demonstrated myocarditis. 10 This case highlights a spectacular example of lymphocytic myocarditis with associated ischemic gastric ulcers, which have not been described in the literature and occur because of severe myocardial dysfunction and resultant cardiogenic shock. A decrease in myocardial contractility leads to diminished cardiac output and subsequent poor perfusion of peripheral tissues. In an attempt to compensate for the decreased circulation, peripheral vasoconstriction transiently improves cardiac function and increases stroke volume until the burgeoning afterload overwhelms the damaged myocardial tissue resulting in end-organ damage and ischemia. Ischemic changes disproportionately affect the gastrointestinal system due to prioritization of systemic over mesenteric circulation. The gastric tissue is further subjected to damage mediated by gastric acid following the compromise of the gastric mucosa. This results in mucosal necrosis/ulceration and loss of glandular architecture, with severe ischemic damage extending into the lamina propria and beyond. 11 This case effectively illustrates the pathophysiology of gastric ischemic ulceration secondary to myocarditis-induced cardiogenic shock, as well as the diagnostic challenges in a clinically diverse disease process, such as myocarditis, especially in the unprecedented setting of the 2019 SARS-CoV-2 epidemic.

Handbook of Pediatric Autopsy Pathology

Pediatric Patients Hospitalized with Myocarditis: A Multi-Institutional Analysis

Clinicopathological features of paediatric deaths due to myocarditis: an autopsy series

Diagnosis of myocarditis: current state and future perspectives

Clinical characteristics of 138 hospitalized patients with 2019 novel coronavirus-infected pneumonia in Wuhan, China

Cardiovascular implications of fatal outcomes of patients with coronavirus disease 2019 (COVID-19)

Coronavirus-induced myocarditis: a metasummary of cases

Cardiac injury, arrhythmia, and sudden death in a COVID-19 patient

Pathological evidence for SARS-CoV-2 as a cause of myocarditis: JACC review topic of the week

A case of viral myocarditis presenting with acute asthma attack

The fundamental hemodynamic mechanism underlying gastric "stress ulceration" in cardiogenic shock