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Complement C9 expression is associated with damaged myocardial cells in pediatric sudden death cases of fulminant myocarditis



Because disease progression is so fast in sudden death of acute fulminant myocarditis, damage of myocardial cells is not evident in routine hematoxylin and eosin staining. To understand damage to myocardial cells and the mechanism of sudden death, immunohistochemical staining was performed for two forensic autopsy cases.

Case presentation

The patients were a healthy 5-year-old girl and 8-year-old boy. They suddenly died within 2 days of appearance of flu-like symptoms. An autopsy showed accumulation of yellowish-clear pericardial fluid containing fibrin deposits, fluid blood in the heart, and congestion of visceral organs. Histologically, minor necrosis or degeneration of myocardial cells with mainly lymphocytic infiltration was observed sometimes in tissue sections. Immunohistochemically, positive complement C9 staining and negative sirtuin 1 staining were found. These findings suggested wide damage of myocardial cells, even in regions with no marked changes in myocardial cells with hematoxylin and eosin staining. These areas corresponded to those with strong accumulation of lymphocytes.


Immunohistochemistry for complement C9 and sirtuin 1 might become a new tool for evaluating damage of myocardial cells of fulminant acute myocarditis.


Acute myocarditis and fulminant myocarditis are relatively rare inflammatory diseases and can become a cause of sudden death (Matsuura et al. 2016). The mortality rate of fatal myocarditis is 0.46 per 10 million patients (Kamiyama 2016). Because the symptoms of myocarditis are widely distributed from mild flu-like symptoms to fatality, clinical diagnosis is difficult owing to its prompt progression (Fuse et al. 2000; Dancea 2001). Clinically, some cases lead to unexpected sudden death and are subsequently diagnosed at forensic autopsy. Diagnosis of myocarditis is based on histological evidence of an inflammatory infiltrate of myocardial cells with necrosis and/or degeneration of adjacent myocytes that is not typical for ischemic damage associated with coronary artery disease (Aretz et al. 1987). However, especially for fulminant cases, damage to myocardial cells is not evident in routine hematoxylin and eosin (HE) staining in some cases because progression of disease is so rapid. Therefore, understanding the mechanism of sudden cardiac death is difficult for these cases.

We report two sudden deaths of children with acute fulminant myocarditis. Novel immunohistochemical methods clearly showed damaged myocardial cells. Our findings will help to understand progression of acute fulminant myocarditis in children.

Case presentation

Case 1

A healthy 5-year-old girl had suffered from mild abdominal pain with a body temperature of 38 °C. The evening after her symptoms appeared, her appetite was lost and general fatigue increased. One day after the appearance of symptoms, she was transferred to a hospital because she was vomiting frequently. At arrival to the hospital, a blood examination showed a white blood cell count of 21,800/μl (normal range 4100–15,000/μl), platelet count of 27.2 × 104/μl (18.0–51.0×104/μl), creatine kinase level of 135 U/I (46–230 U/I), and C-reactive protein level of 3.2 mg/dl (> 1.29 mg/dl). A volume of 1000 ml of fluid infusion with 10 mg of metoclopramide improved her general condition, and she returned home. However, her general condition worsened again and frequent vomiting and abdominal pain appeared. Therefore, she was transferred to the hospital again. Before arriving at the hospital, she was in cardiopulmonary arrest. In spite of resuscitation attempts, she was pronounced dead 2 days after appearance of the initial symptoms. A forensic autopsy was performed the next day. Her height was 114 cm and weight was 18.6 kg. No marked abnormalities were found externally. The heart weighed 104.3 g and contained blood, with 15 ml in the right atrium and 5 ml in the left atrium. A volume of 50 ml of yellowish-clear pericardial fluid containing fibrin deposits was also found. Other organs showed marked congestion without any abnormalities. A histological examination was performed, and the bottom and outlet of the right ventricle, anterior wall, posterior wall, septum, and outlet of the left ventricle were examined. Minor necrosis and degeneration of myocardial cells were observed sometimes in tissue sections, with a lot of lymphocytic infiltration and a few areas of neutrophilic infiltration in the interstitial spaces in each location. However, these findings were marked, especially in four locations in the left ventricle (Figure 1a). No bacteria were detected by a blood culture. Toxicologically, neither alcohol nor other illicit drugs were found in the blood or urine. A viral examination was not performed because of the limited amount of blood. Finally, she was diagnosed as dying from acute fulminant myocarditis.

Fig. 1
figure 1

Histopathological findings of the left ventricle in case 1 (a) and case 2 (b). In myocardial cells of both cases, myocardial cells with minor necrosis and degeneration were observed sometimes in tissue sections, with a lot of lymphocytic infiltration and a few areas of neutrophilic infiltration in the interstitial spaces (magnification, × 400)

Case 2

A healthy 8-year-old boy had suffered from general fatigue with a body temperature of 39.6 °C. The next day after appearance of these symptoms, his general condition did not improve and a temperature of 38.6 °C persisted. At noon, he suddenly deteriorated and was immediately transferred to the hospital. At arrival to the hospital, he suffered from ventricular tachycardia. Although a resuscitation attempt was performed, he was soon pronounced dead. A forensic autopsy was performed the next day. His height was 122 cm and body weight was 22.4 kg. No external abnormalities were found. The pericardial cavity contained 12 ml of yellowish-clear fluid with fibrin deposits. A volume of 100 ml of dark red blood was found in the heart cavities. The heart weighted 134.5 g and showed petechial hemorrhage on the surface of the visceral pericardium, but it was otherwise normal. Histologically, myocardial cells with minor necrosis and degeneration were observed sometimes in tissue sections. There was also a lot of lymphocytic infiltration and a few areas of neutrophilic infiltration in the interstitial spaces of the bottom and outlet of the right ventricle, anterior wall, posterior wall, septum, and outlet of the left ventricle (Fig. 1b). The histological features were similar for six locations. A serological examination did not show adenovirus, influenza A or B, coxsackie A, rotavirus, or respiratory syncytial viruses. Toxicologically, except for acetaminophen and lidocaine, which were used for medical intervention, no drugs and alcohol were detected from the blood. Finally, he was diagnosed with acute fulminant myocarditis.


Immunohistochemical staining for complement C9 (CC9) and sirtuin 1 (SIRT1) was performed. We prepared 5-μm paraffin sections of the heart in the two patients by dewaxing, rehydrating, and treating with 0.3% H2O2 for 30 min to block endogenous peroxidase. For antigen retrieval, the sections were autoclave-treated in citrate buffer at pH 6.0 for 10 min and allowed to cool for 30 min. The sections were incubated at room temperature with 10% normal rabbit serum or 10% normal goat serum (Nichirei Co., Ltd., Tokyo, Japan) for 10 min. A mouse monoclonal antibody against CC9 (clone 10A6, 1:2000 dilution; MAB9622; Abnova, Taipei City, Taiwan) or a rabbit monoclonal antibody against SIRT1 (clone E104, 1:2000 dilution; NB110-57573; Novus Biologicals, CO, USA) was then applied with incubation overnight at 4 °C. Indirect immunostaining was achieved using the streptavidin-biotin-peroxidase technique. Peroxidase was developed using a diaminobenzidine kit (Peroxidase Stain DAB Kit [Brown Stain]; Nacalai Tesque, Kyoto, Japan). As a negative control, the heart of a child who died in a traffic accident was used. The sections were also lightly counterstained with hematoxylin.

For the six locations of the heart, CC9-positive staining was observed in the cytoplasm. However, these stained regions did not correspond to abnormalities of HE staining. The positive areas corresponded to those of strong accumulation of lymphocytes. SIRT1-positive regions were found for most of the cytoplasm of myocardial cells, but SIRT1 staining was negative in CC9-positive regions (Fig. 2). The CC9-positive regions were more marked observed in case 2 than in case 1. In case 1, the CC9-positive region was marked in the septum and outlet of the left ventricle; in case 2, marked in the septum and posterior wall of the left ventricle.

Fig. 2
figure 2

Images of immunohistochemical staining in myocardial cells in case 1 (a–c) and case 2 (d–f). a, d Hematoxylin and eosin staining. b, e Immunohistochemistry for Complement C9. c, f Immunohistochemistry for Sirtuin I (magnification, × 200)


In our two cases, the patients suddenly died with short clinical courses. The cause of death was determined by forensic autopsies. Myocarditis is found as a potential cause of death in 3.7% of sudden infant death syndrome cases (Grasmeyer and Madea 2015). As shown in our cases, performing forensic autopsies for unexpected death in children is important (Weber et al. 2008).

Generally, postmortem diagnosis of myocarditis is based on necrosis and/or degeneration of myocytes and adjacent inflammatory infiltrates (Aretz et al. 1987; Aretz 1987). However, histopathological diagnosis by routine HE staining remains difficult for some sudden death cases, especially for fulminant cases with short clinical courses. Our two patients showed remarkably similar clinical presentations. The pathological findings with HE staining also showed similar results of degeneration and necrosis of myocytes with dense lymphocytic infiltration in the interstitial spaces.

For sudden death by fulminant myocarditis, necrosis/degeneration of myocardial cells is not obvious in HE-stained specimens. Several types of immunohistochemical staining are applied to acute myocarditis for detecting changes in . Expression of tumor necrosis factor-α (TNF-α) has been examined in the myocardium in human myocarditis (Jibiki et al. 2000). TNF-α is mainly localized in cardiac myocytes and blood vessels and not in infiltrated mononuclear cells. Although TNF-α has multiple actions that mediate the pathogenic processes of cancer, septic shock, and inflammation, the authors speculate that expression of TNF-α in fatal human myocarditis may act as a myocardial depressant. Additionally, immunostaining of tenascin-C has been applied for human acute myocarditis cases (Morimoto et al. 2005; Imanaka-Yoshida et al. 2002). Positive staining for tenascin-C is localized in the vicinity of damaged myocardial cells and it reflects disease activity. The authors consider that although expression of tenascin-C is not a specific finding for myocarditis, it is associated with injury and inflammation caused by various pathogeneses.

Recently, immunohistochemical staining of the heart has been applied for sudden death cases and morphological changes in acute death have been evaluated. CC9 is useful for detecting acute myocardial damage. When abnormalities are not detected in HE staining in acute myocardial infarction within 6 h of onset, positive findings of CC9 are observed (Jasra et al. 2012). Furthermore, SIRT1, which modulates cellular adaptation to hypoxia by targeting hypoxia-inducible factor α, is also useful for detecting damaged myocytes. SIRT1 is highly expressed in the normal heart and regulates a wide array of cellular process and cardiac electrical activity, and plays a major role in progression of heart failure (Vikram et al. 2017; Tanno et al. 2012). With regard to sudden death due to ischemic heart disease, we barely had obtained typical pathological changes because of the short survival period. However, CC9-positive and SIRT1-negative findings show acute damage of myocardial cells (Morita et al. 2015a; Morita et al. 2015b). In this study, we confirmed that this immunohistochemical approach is useful for detecting damaged myocytes, even for sudden death by myocarditis. In this approach, because damaged myocardial cells are more obvious than with other immunohistochemical stains in acute myocarditis, we can easily understand the reason for sudden cardiac arrest. Although CC9 or SIRT1 expression is not a specific finding for myocarditis, immunohistochemistry for CC9 and SIRT1 might become a new tool for evaluating damage of myocardial cells of fulminant acute myocarditis. As a limitation, number of cases was not enough to recommend these immunohistochemical stains for fulminant myocarditis. However, authors believe this study was a potentially important prelude to further studies of the utility of these immunohistochemical stains. In the future, this immunohistochemical approach should be performed for other sudden death cases of myocarditis to validate our findings.

Availability of data and materials

The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.



Hematoxylin and eosin


Complement C9


Sirtuin 1


Tumor necrosis factor-α


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Author information




ATU and MH performed the autopsies and drafted the manuscript; TM and YH examined the clinical course of patients; ATU performed pathological examination; MH reviewed the work critically for important intellectual content; MN performed histological analysis; TN drafted the figures and the manuscript; TM and YH acquired and analyzed the data. The authors read and approved the final manuscript.

Corresponding author

Correspondence to Masahito Hitosugi.

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This study was approved as reference number R2014-010 by Shiga University of Medical Science Research Ethics Committee.

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Uno, A.T., Hitosugi, M., Nakamura, M. et al. Complement C9 expression is associated with damaged myocardial cells in pediatric sudden death cases of fulminant myocarditis. Egypt J Forensic Sci 10, 37 (2020).

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  • Autopsy
  • Case report
  • Child
  • Complement C9
  • Immunohistochemistry
  • Myocarditis
  • Sirtuin 1
  • Sudden death