Cardiac rhabdomyoma in a slaughtered pig/Rabdomioma cardiaco em um suino de abate.
Cardiac rhabdomyoma is characterized by large glycogen containing vacuolated cells and is also referred to as rhabdomyomatosis, congenital glycogen tumor, circumscribed glycogen storage disease, nodular glycogen degeneration, nodular glycogen, and nodular glycogen infiltration (KIZAWA et al., 2002). Cardiac rhabdomyoma must be differentiated from glycogen storage disease (WALVOORT, 1983) and other differential cardiac tumors as lymphoma, hemangiosarcoma and hemangioma (LOYNACHAN, 2012). This report describes the histopathological and immunohistochemical findings of a case of cardiac rhabdomyoma in a slaughter pig.
A male pig of commercial lineage and slaughter age (165-170 days) was shipped to the slaughterhouse and found dead in the transport truck during pre-slaughter handling. The pig was submitted to routine necropsy examination, and macroscopically the heart was moderately globose, there was stomach ulcer and cranioventral pulmonary consolidation, all other organs had no significant gross lesions. On the cut surface of the ventricular walls, a nodule of 2.0x1.5cm was observed in the right ventricle, extending from the myocardium to the ventricular chamber (Figure 1A). The nodule was circumscribed, well demarcated, apparently encapsulated, yellowish-white, and firm. Multiple nodules, varying from 0.3 to 0.5 cm in diameter and similar in appearance to the right ventricular nodule, were also observed in the left ventricular myocardium and the interventricular septum. Representative samples of all organs were fixed in 10% formalin, and the tissues were processed routinely and embedded in paraffin. Three micrometer sections of the paraffin blocks were made and stained with hematoxylin and eosin (HE) and Schiff's periodic acid (PAS). Serial sections were subjected to immunohistochemistry (IHC), with the following antibodies, according to previously described protocols (PEREIRA et al., 2017): vimentin (clone V9; 1:200; Zymed), pan-cytokeratin (clone AE1/AE3; 1:80; DakoCytomation) and neuron specific enolase (NSE) (1:200; DakoCytomation). Antibodies of desmin and atrial natriuretic peptide (ANP) according to described protocols (CRUZ, 2017): desmin (1:300; DakoCytomation) and ANP (1:50; Abcam). The detection method and chromogen, used for all antibodies were the Labelled Streptavidin-Biotin System-Horseradish Peroxidase (DakoCytomation) and 3,3'-diaminobenzidine (DAB) (DakoCytomation), respectively.
Microscopically, a neoplastic proliferation well circumscribed but not encapsulated, composed by polyhedral cells was observed, arranged in cohesive bundles interspersed with scarce fibrovascular stroma. Cells had distinct borders with ample eosinophilic cytoplasm that often contained multiple vacuoles. Some cells had a centrally-located nucleus, with lacy cytoplasm, giving the appearance of a "spider cell". The nuclei were oval with finely dotted chromatin and unique nucleoli. There was moderate anisocytosis and anisokaryosis. Mitotic figures were not observed (Figure 1B). Areas of pulmonary consolidation corresponded microscopically to necrotizing bronchiolitis compatible with Influenza pneumonia.
On PAS staining, glycogen granules were detected in the cytoplasm of the neoplastic cells. Neoplastic cells were also positive for desmin (Figure 1C), NSE (Figure 1D), ANP (Figure 1E), and vimentin (Figure 1F) by IHC to varying degrees. Discrete immunoreactivity was observed for vimentin, moderate for ANP, and accentuated for desmin and NSE, whereas there was no immunolabeling for pan-cytokeratin.
The diagnosis of cardiac rhabdomyoma in this study was based on the pathological and immunohistochemical findings. Neoplasm was observed in a slaughter pig, generally is considered an incidental slaughter lesion (COOPER & VALENTINE (2017), but in this case, the neoplasm associated with stomach ulcer and the Influenza lesions observed in the lung contributes to the pig death. Sudden death may occur due to the interference in the myocardial conduction that these tumors can potentially cause, as suggested by MCE WEN (1994). Mortality in transported pigs may still occur due to stress, mainly caused by ambient temperature and transport distance (VOSLAROVA et al., 2017).
The present report describes a multifocal distribution of neoplastic nodules, the largest of which was in the right ventricle; however, MCEWEN (1994) reported that rhabdomyoma is more common in the left ventricle, but also it can be observed in the interventricular septum and the right ventricle (TANIMOTO & OHTSUKI, 1995). On gross examination nodules, 0.3 to 2.0cm in diameter, were observed and were well delimited, firm, and yellowish-white, similar to those previously described (OMAR, 1969; TANIMOTO & OHTSUKI, 1995; KIZAWA et al., 2002; KOLLY et al., 2004; JACOBSEN et al., 2010; KRAFSUR et al., 2014). When the nodules project into the chamber, they are very susceptible to hemorrhage and necrosis and may become cystic (ROBINSON & ROBINSON, 2016); however, cyst formation, hemorrhage and necrosis were not observed in this case.
Histologically, neoplastic cells had markedly distended cytoplasm that was eosinophilic and often vacuolated, as is described in cases of other species (OMAR, 1969; JACOBSEN et al., 2010; KRAFSUR et al., 2014). The described "spider cells" were also observed in other reports (OMAR, 1969; TANIMOTO & OHTSUKI, 1995; KOLLY et al., 2004; JACOBSEN et al., 2010) and, this aspect occur after routine processing, which causes the loss of glycogen (TANIMOTO & OHTSUKI, 1995; RADI & METZ, 2009). ROBINSON & ROBINSON (2016) also described areas of fibrosis, however they were not observed in this case.
Cardiac rhabdomyoma must be differentiated from glycogen storage disease, which is characterized by accumulation of glycogen in the heart, skeletal muscle, liver, kidneys, or muscle layer of the esophagus (WALVOORT, 1983), in this case we did not observe lesions in other organs. Other differential cardiac tumors are lymphoma, hemangiosarcoma and hemangioma (LOYNACHAN, 2012).
On PAS staining, glycogen granules were detected in the cytoplasm of the neoplastic cells, confirming glycogen content similar to that observed in several studies (OMAR, 1969; TANIMOTO & OHTSUKI, 1995; KIZAWA et al., 2002; KOLLY et al., 2004; RADI & METZ, 2009; JACOBSEN et al., 2010; KOBAYASHI et al., 2010). Immunoreactivity was observed in the cytoplasm of the neoplastic cells for desmin, NSE, ANP, and vimentin, as described by other authors (JACOBSEN et al., 2010; EL SHARABY et al., 2001). Discrete immunoreactivity for vimentin and accentuated for desmin and NSE was also describe by JACOBSEN et al. (2010). As reported by TANIMOTO & OHTSUKI (1995), there was no immunolabeling for cytokeratin.
The histogenesis of rhabdomyoma is still uncertain, some authors suggest that they are hamartomas (ROBINSON & ROBINSON, 2016), while others have investigated whether the cells are derived from the striated myocardium (COOPER & VALENTINE, 2017) or Purkinje fibers (TANIMOTO & OHTSUKI, 1995). To confirm the origin, studies have been performed, in which ANP immunolabeling has already been observed in the Purkinje fibers of different species (HANSSON et al., 1997). BIONDO et al. (2003) demonstrated ANP immunoreactivity was restricted to the atria, no marked in ventricular cardiomyocytes of healthy cats. TANIMOTO & OHTSUKI (1995) demonstrated that immunoreactivity for vimentin may reflect the development of Purkinje fibers from multipotent cardiomyocyte precursors during embryogenesis. Based on the immunohistochemical findings in this case that are, very similar to those observed by JACOBSEN et al. (2010), with immunoreactivity in the neoplastic cells for desmin, NSE, ANP, and vimentin, suggested that the tumor in this case originated from the Purkinje fibers.
The authors are grateful to Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq) and Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior (CAPES).
BIOETHICS AND BIOSSECURITY COMMITTEE APPROVAL
We authors of the article entitled "Cardiac rhabdomyoma in a slaughter pig" declared, for all due purposes, the project that gave rise to the present data of the same has not been submitted for evaluation to the Ethics Committee of the Universidade Federal do Rio Grande do Sul (UFRGS), but we are aware of the content of the Brazilian resolutions of the Conselho Nacional de Controle de Experimentacao Animal (CONCEA) <http://www.mct.gov.br/ index.php/content/view/310553.html> if it involves animals. Thus, the authors assume full responsibility for the presented data and are available for possible questions, should they be required by the competent authorities.
DECLARATION OF CONFLICTING INTERESTS
The authors declare no conflict of interest. The founding sponsors had no role in the design of the study; in the collection, analyses, or interpretation of data; in the writing of the manuscript, and in the decision to publish the results.
The authors contributed equally to the manuscript.
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Paula Reis Pereira (1) * Raquel Aparecida Sales da Cruz (2) Luciane Maria Juhlich (3) Luciana Sonne (1) David Emilio Santos Neves de Barcellos (3) David Driemeier (1)
(1) Setor de Patologia Veterinaria, Faculdade de Veterinaria, Universidade Federal do Rio Grande do Sul (UFRGS), 91540-000, Porto Alegre, RS, Brasil. E-mail: firstname.lastname@example.org. Corresponding author.
(2) Laboratorio de Patologia Veterinaria, Hospital Veterinario, Universidade de Cuiaba (UNIC), Cuiaba, MT, Brasil.
(3) Setor de Suinos, Faculdade de Veterinaria, Universidade Federal do Rio Grande do Sul (UFRGS), Porto Alegre, RS, Brasil.
Caption: Figure 1-Cardiac rhabdomyoma in a slaughter pig. (A) Nodule of 2.0x1.5cm observed in the wall of the right ventricle (arrow). Inset: nodule was circumscribed and yellowishwhite. Bar: 2.0cm. (B) Neoplasm composed of polyhedral cells with ample eosinophilic cytoplasm that is often vacuolated, with some cells presenting "spider cell" appearance. HE, Bar: 200 [micro]m. (C) Neoplastic cells positive for desmin, with some cells presenting "spider cell" appearance (arrow). Chromogen DAB, Bar: 100 [micro]m. (D) Accentuated immunoreactivity for NSE in the neoplastic cells. Chromogen DAB, Bar: 100 [micro]m. (E) Moderate immunoreactivity for ANP in the neoplastic cells. Chromogen DAB, Bar: 100 [micro]m. (F) Discrete immunoreactivity for vimentin in the neoplastic cells. Chromogen DAB, Bar: 100 [micro]m.
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|Author:||Pereira, Paula Reis; da Cruz, Raquel Aparecida Sales; Juhlich, Luciane Maria; Sonne, Luciana; de Bar|
|Date:||Oct 1, 2018|
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