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On-line version ISSN 1678-9849
Rev. Soc. Bras. Med. Trop. vol.36 no.4 Uberaba July/Aug. 2003
Estudo morfométrico da fibrose e do número de mastócitos na muscular circular do cólon de chagásicos crônicos com e sem megacólon
Simone Wanderley Pinheiro; Adilha Misson de Oliveira Rua; Renata Margarida Etchebehere; Cristiane Gobbo Cançado; Javier Emílio Lazo Chica; Edison Reis Lopes; Sheila Jorge Adad
Disciplina de Patologia Especial e Curso de Pós-Graduação em Patologia da Faculdade de Medicina do Triângulo Mineiro, Uberaba, MG
A morphometric study of the circular colon musculature was performed, in which the mast cell count was determined and the connective fibrous tissue in this layer was measured. The objective was to gain better understanding of Chagas megacolon morphology and contribute towards the knowledge of fibrosis pathogenesis in Chagas megas. An evaluation was made of 15 distal sigmoid rings from Chagas patients with megacolon (MCC), 15 without megacolon (CSMC) and 15 non-Chagas patients (NC). The rings were fixed in formol, embedded in paraffin, and 7mm thick sections were cut and stained using Azan-Heidenhain and Giemsa. The mast cell count and fibrosis were greater in the MCC group than in the CSMC and NC groups (p < 0.05; Kruskal-Wallis test) and there was no significant difference between the latter two. The fibrosis and increased mast cell count in the colon musculature of the MCC group possibly indicates that there is a relationship between mastocytosis and fibrosis, as has already been demonstrated in other pathologies.
Keywords: Megacolon. Mast cell. Fibrosis. Morphometry. Chagas' disease.
Com os objetivos de conhecer melhor a morfologia do megacólon chagásico e contribuir para o conhecimento da patogênese da fibrose dos megas, realizou-se estudo morfométrico na muscular circular do cólon, contando-se o número de mastócitos e medindo o conjuntivo fibroso nessa camada. Foram avaliados anéis do sigmóide distal de 15 chagásicos com megacólon (MCC), 15 sem megacólon (CSMC) e 15 não chagásicos (NC). Os anéis foram fixados em formol, incluídos em parafina, cortados com 7mm de espessura e corados por Azan-Heidenhain e Giemsa. O número de mastócitos e a fibrose foram maiores no grupo com MCC em relação ao CSMC e NC (p < 0,05; teste de Kruskal-Wallis); não houve diferença significante entre os dois últimos grupos. Diante destes achados, é possível, que haja relação entre mastocitose e fibrose no megacólon chagásico, como já se demonstrou em outras doenças.
Palavras-chaves: Megacólon. Mastócito. Fibrose. Morfometria. Doença de Chagas.
Muscle layer alterations such as myositis and fibrosis that could contribute to the pathogenesis of Chagas' disease megas are often found both in the esophagus1 3 16 and in the colon2 16. According to Tafuri and Raso16, fibrosis in Chagas megaesophagus sometimes is focal, possibly representing a sequel of myositis and thought to be associated with mast cell infiltrate, and sometimes is diffuse and interstitial without showing a topographic relationship with the inflammation. Andrade & Andrade8, analyzing myocardial fibrosis, also accepted that focal fibrosis could result from scarring of inflammatory foci related to the presence of mast cells. Nonetheless, Andrade & Andrade8 stressed that the pathogenesis of diffuse interstitial fibrosis had not been clarified.
Quantitative studies made on cardiopathic Chagas' disease patients7 and on the circular esophagus musculature of chronic Chagas patients without megaesophagus11, have reported a marked increase in the mast cell count in these organs. However, no statistical difference has been detected between the mast cell counts in the musculature of the esophagus5 and colon4 of chronic Chagas patients with and without megas, in relation to non-Chagas patients.
With regard to experimental Chagas' disease, there has been a report of increased mast cell count in areas of reinoculation with Trypanosoma cruzi on the skin of mice10. Increased mast cell count has also been found in the submucosa and especially the musculature of the small and large intestines of mice chronically infected with the ABC strain of T. cruzi14. Chapadeiro et al9 reported that, in albino Wistar rats infected experimentally with T. cruzi, mast cells were absent or rare in the infected animals in the acute phase. Pinheiro et al12 demonstrated in rats chronically infected with T. cruzi that there was an increased mast cell count in the myocardium, although no relationship with fibrosis could be shown.
The data regarding the increase in mast cell count is controversial and there is a lack of morphometric studies on fibrosis in the musculature of the digestive tract of chronic Chagas patients. In view of this, we have made a morphometric evaluation of the fibrosis and mast cell count in the circular colon musculature of chronic Chagas patients with and without megas. Our objective was to gain better understanding of Chagas megacolon morphology and contribute towards the knowledge of fibrosis pathogenesis in megas.
MATERIAL AND METHODS
It was necessary that two of the three following tests were positive in the serum or in the pericardial fluid for the diagnostic of infection with Trypanosoma cruzi: ELISA (Enzyme-Linked-Immunosorbent-Assay), passive hemagglutination and indirect immunofluorescence to T. cruzi. The individuals of the control groups had the three tests negative.
Forty-five segments of large intestine were obtained via surgery and/or necropsy performed in the Pathology Service of the University Hospital of FMTM, Uberaba, Minas Gerais. Of these 45 cases, 30 individuals were chronic Chagas patients and 15 were non-Chagas patients without any intestinal pathology, who served as controls. The 30 Chagas patients were subdivided into two groups: with megacolon, consisting of 15 individuals, and without megacolon, also consisting of 15 cases.
In each case, a ring of around 0.5cm in height was removed from the rectosigmoid transition. The rings were fixed in 4% formol and, after fixing, dehydrated, diaphanized and embedded in paraffin to form blocks measuring up to 5x5cm for microtomy. Histological sections with 7mm in thickness were cut and stained using hematoxylin-eosin, Azan-Heidenhain and Giemsa techniques. The sections stained using the hematoxylin-eosin were only utilized for a general analysis of the rings. Following this, a quantitative analysis of the fibrosis was made on the sections stained using the Azan-Heidenhain technique and an counting of the mast cells on sections stained using the Giemsa technique.
The count of mast cells in the circular musculature was done using an standard optical microscope coupled to a video camera linked to a high-resolution monitor. The image obtained on the monitor was integrated with a cursor that could move across a graphical measuring grid connected to an automatic image analysis system of Leica Q 500MC brand. The count was done manually, while the area that was being evaluated was standardized.
The histological sections were previously marked at eight locations that were approximately equidistant from each other. The mast cells were counted in 40 consecutive fields of each subdivision, making a total of 320 microscope fields with the 10x eyepiece and 40x objective lens, corresponding to a total area of 4mm².
For the analysis of the fibrosis, the histological sections were again previously marked at eight locations that were approximately equidistant between each other. The fibrosis was measured in 10 alternate fields in each subdivision, making a total of 80 microscope fields covering a total area of 1mm². This analysis was also done with the 10x eyepiece and 40x objective lens. The same morphometry apparatus was utilized as described for the mast cell analysis (Figures 1A, 1B and 1C).
The variables analyzed were submitted to statistical analysis via the Kruskal-Wallis and Dunn tests. The significance level considered for the tests was 5% (p < 0.05). To evaluate whether there was a relationship between the fibrosis percentage and the mast cell count, the Spearman test was utilized.
This research was approved by the Research Ethics Committee of Faculdade de Medicina do Triângulo Mineiro (FMTM), Uberaba, Minas Gerais.
The mast cells were found to be dispersed over the whole muscle tunica in all groups, generally without forming accumulations (Figures 2A and 2B). In the megacolon group there were mast cells both at the myositis foci (Figure 2D) and dispersed over the remainder of the musculature (Figure 2C).
In the non-Chagas group, no myositis was identified. In the Chagas group without megacolon, discrete myositis was found in four cases (30.1%) (nos. 17, 20, 22 and 23). In the megacolon group there was myositis in 14 of the 15 cases (93.3%), which was discrete in one case (no 39), moderate in 6 cases (Nos 31, 38, 42, 43, 44 and 45) and severe in 7 cases (nos 32, 33, 34, 35, 36, 37 and 40).
As indicated in Table 1, the mast cell count found in the circular colon musculature was significantly greater in the Chagas group with megacolon than in the other groups. When pairs of groups were analyzed together, it was noted that the mast cell count was greater in the Chagas group with megacolon in comparison with the Chagas group without megacolon (p < 0.01) and the non-Chagas group (p < 0.01). However, there was no significant difference between the non-Chagas group and the Chagas group without megacolon (p > 0.05).
With regard to fibrosis, fibrous connective tissue in the muscle tunica was rare in the non-Chagas group and was represented by thin bands between the myocells (endomysial connective tissue) and between the muscle bundles (perimysial connective tissue) (Figure 3A).
In the Chagas group without megacolon, the appearance of the connective tissue in the muscle tunica was similar to that described for the non-Chagas individuals (Figure 3B). In the Chagas group with megacolon, there was an evident diffuse increase in endomysial and perimysial connective tissue and frequent substitution fibrosis foci (Figures 3C and 3D).
As can be seen in Table 2, there was a statistically significant difference between the groups. The percentage of fibrous connective tissue was greater in the megacolon group, in comparison with the Chagas group without megacolon (p <0.001) and the non-Chagas group (p < 0.001). However, there was no statistically significant difference between the non-Chagas group and the Chagas group without megacolon (p > 0.05).
The value for the Spearman correlation coefficient between the mast cell count and the percentage of fibrous connective tissue for the Chagas group with megacolon was -0.2, which was not statistically significant (p > 0.05). However, when we analyzed the Chagas groups with and without megacolon together, the value for the correlation coefficient between the mast cell count and the percentage of fibrous connective tissue was 0.215, which was statistically significant (p < 0.05), (table 3, 4 and 5).
Our data are in agreement with quantitative studies of mast cells in the human myocardium7 and in the myocardium of rats with chronic Chagas' disease via experimental infection12. The data also agree with the description of increased mast cell counts in the circular musculature of the small and large intestines in mice with chronic Trypanosoma cruzi infection14.
Our data disagree with the quantitative studies made by Adad et al4 5 on the circular musculature of the esophagus and colon of chronic Chagas cases with or without megas. It is possible that these authors did not find significant differences between the groups because they analyzed a lesser number of microscope fields and cases.
With regard to the results from counting mast cells in the musculature of the esophagus of chronic Chagas cases obtained by Pereira et al11, they appear at first to agree with those obtained in our study. However, those authors only evaluated the esophagus of Chagas cases without megas. In our material, we only observed a statistically significant difference in the group with megacolon, while the Chagas cases without megacolon did not present any significant difference when compared with the non-Chagas patients. We must stress that those authors worked with a greater number of cases and, in addition to this, there may be differences between how the esophagus and colon musculatures are compromised. It has already been demonstrated that myositis occurs more frequently and severely in the esophagus than in the colon of chronic Chagas cases6.
With regard to the morphometric analysis of fibrosis that was done in this study, we demonstrated that in the colon musculature there was a greater percentage of fibrous connective tissue in the Chagas group with megacolon, in comparison with the Chagas group without megacolon and the non-Chagas group. We did not find in the literature any morphometric studies of fibrosis in the colon of Chagas cases. Nonetheless, our findings are in agreement with the observations of Adad2, who described fibrosis in the muscle tunica of Chagas megacolon that was often moderate to severe, and also with the ultrastructural megaesophagus data of Tafuri et al15 and Tafuri13.
Our results appear to support the hypothesis that interstitial fibrosis is related to the mastocytosis present in experimental and human Chagas' disease, since we found greater mast cell counts in the muscle tunica of the group with megacolon, in relation to the others. Nevertheless, when we analyzed each group of Chagas cases separately, it was not possible to demonstrate a relationship between mast cells and fibrosis, perhaps because of the small number of cases. However, when we analyzed the Chagas groups with and without megacolon together, we observed a significant relationship between the mast cell count and the percentage of fibrous connective tissue.
In conclusion, the analysis of the findings of this study and the data in the literature demonstrate that there is a greater mast cell count and more fibrosis in Chagas cases with megacolon. However, it was not possible to demonstrate whether there is a relationship between the fibrosis and the mast cell count, as suggested by some data in the literature, perhaps because of the sample size.
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Dra Sheila Jorge Adad
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Recebido para publicação em 25/10/2002
Aceito em 6/6/2003
Financial support: FAPEMIG (project no. CDS 2835/98) and CNPq