Authors

  • К. Chartaqov
    Andijan State Medical Institute
  • Х. Chartaqova
    Andijan State Medical Institute
  • А. Chartaqov
    Andijan State Medical Institute

DOI:

https://doi.org/10.71337/inlibrary.uz.ijms.76188

Abstract

Morphological and histochemical structural changes of the wall and its lymphatic bed were studied in 104 dogs after gastric resection, after surgery there was also an increase in the diameter of lymphatic catillaries and vessels. There are lateral dilatations and dislocations in the walls of the capillaries, new anastomoses of all the membranes are formed, for the most part they break out in the mucous membrane. Pathohistological changes in the wall of the small intestine will appear in the form of edema of the mucous membrane, vascular fullness, lymphatic infiltration and changes in the shape of the villi.

 

 

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CERTAIN PATTERNS OF CHANGES IN THE LYMPHOCIRCULATORY

NETWORK OF THE INTESTINE AFTER GASTRECTOMY

Chartaqov К.Ch., Chartaqova Х.Х., Chartaqov А.К.

Andijan State Medical Institute

Annotation:

Morphological and histochemical structural changes of the wall and its

lymphatic bed were studied in 104 dogs after gastric resection, after surgery there was also

an increase in the diameter of lymphatic catillaries and vessels. There are lateral dilatations

and dislocations in the walls of the capillaries, new anastomoses of all the membranes are

formed, for the most part they break out in the mucous membrane. Pathohistological

changes in the wall of the small intestine will appear in the form of edema of the mucous

membrane, vascular fullness, lymphatic infiltration and changes in the shape of the villi.

Key words:

stomach, lymphatic system, resection, duodenum, pathomorphological changes.

Despite the significant number of studies devoted to the investigation of the lymphatic

system of the gastrointestinal tract under various pathological conditions, certain questions

remain unresolved. This is especially true regarding changes in the lymphatic network of the

small intestine after different types of gastrectomy procedures [2,3,5]. Gastrectomy,

regardless of the method used, is accompanied not only by the removal of a significant

portion of the organ but also by damage to nerves and blood vessels. This undoubtedly

affects the morphological condition of the lymphatic network, not only of the stomach itself

but also of other abdominal organs. Therefore, the issues related to lymphatic system

pathology associated with damage to the digestive tract—particularly due to gastrectomy—

remain highly relevant [1,4].

Objective of the Study:

To investigate the morphological and functional changes in the

intestinal wall and its lymphatic network after various types of gastrectomy.

Materials and Methods:

The study was conducted on 122 mongrel dogs. Of these, 104

animals underwent gastrectomy using the following techniques: Billroth I, Kupriyanov-

Zakharov, Hofmeister–Finsterer, and Polya–Reichel. The remaining 18 animals served as

the control group.

To study the structural changes in the lymphatic vessels of the small intestine, animals were

euthanized at 3, 7, 15 days; 1, 1.5, 2, 3, and 6 months; and 1 year after gastrectomy. At the

end of each experimental period, animals were euthanized via overdose of narcotic agents

(hexenal or thiopental sodium). Intra-organ lymphatic vessels were examined using an

isolated segment of the small intestine, 12–15 cm in length, taken 35–40 cm from the

duodenojejunal flexure. These vessels were filled with Gerota’s mass via interstitial

injection. Then, clarified specimens were prepared and studied under an MBS-2 binocular

microscope.

In the examination of 492 specimens

obtained from 82 dogs, attention was paid to the

external structure, orientation of the lymphatic vessels and their loops, the presence of

anastomoses, and the density of the vascular pattern. The diameters of lymphatic loops,


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capillaries, and vessels, as well as the protrusions and lateral bulges on their walls, were

measured — a total of 37,520 measurements were performed.

To study the pathohistological and histochemical structures of the small intestine walls,

samples were taken from 2 dogs in each group at 3, 7, 15, and 30 days after gastrectomy (a

total of 32 animals). Histological and histochemical examinations of the intestinal wall were

conducted. For microscopic examination, tissue samples were taken from the initial section

of the small intestine. The samples were fixed in a 10% solution of neutral formalin, passed

through a series of alcohols, and embedded in paraffin. The resulting 6–8 μm thick sections

were stained with hematoxylin-eosin and by Van Gieson's method, and PAS (Periodic Acid–

Schiff) reaction was applied.

Quantitative indicators were statistically analyzed using the “ES-1020” computer system.

Significance was accepted at levels of P < 0.05, P < 0.01, and P < 0.001.

Research results and discussion:

It was found that, at various intervals after gastrectomy,

the restructuring of the lymphatic network is characterized by an increase in the density of

the network across all layers of the intestinal wall. The most significant changes occurred in

the lymphatic network of the mucous membrane. These capillaries were dilated and

convoluted. In some areas, they were swollen and formed anastomoses at different levels.

The loops varied in shape, with the following average dimensions: length — 61.0 ± 3.0 μm

(P < 0.001), width — 39.0 ± 1.0 μm (P < 0.001).

In the muscular layer, a distinct capillary network was present. The capillary diameter was

29.0 ± 4.0 μm (P < 0.001). The loops they formed had an oval-elongated shape, with a length

of 12.0 ± 3.0 μm (P < 0.001) and a width of 6.0 ± 2.0 μm (P < 0.001); their orientation

matched the alignment of muscle fibers. Compared to the loops of the muscular layer in

control animals, an increase in size was observed, which was associated with an increased

diameter of the capillaries themselves.

Lymphatic capillaries and vessels forming networks and plexuses in the serous membrane

had varying contours and were dilated. The capillaries reached a diameter of 3.0 ± 3.0 μm (P

< 0.001) and formed small oval-shaped loops with the following dimensions: length —

98.0 ± 3.0 μm (P < 0.001), width — 61.0 ± 2.0 μm (P < 0.001). Wide lacunae of various

shapes were frequently observed. The lymphatic vessels were dilated, with a diameter of

41.0 ± 1.0 μm (P < 0.001), and the distance between valves in their lumen decreased to

247.0 ± 3.0 μm (P < 0.001).

At later time points, further remodeling of the lymphatic capillaries and vessels of all layers

of

the

small

intestine

was

observed

(see

Fig.

1,

0).

In the mucosal layer, the caliber of lymphatic capillaries and vessels decreased, but the

network became denser. Outgrowths on their walls were more frequently detected, and the

loops had a polygonal shape with the following dimensions: length — 111.0 ± 2.0 μm (P <

0.001), width — 49.0 ± 2.0 μm (P < 0.001).

In the submucosal layer, lymphatic capillaries formed a dense network with smooth walls

and no outgrowths. Capillary lacunae were reduced and had irregular or oval shapes. The


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loops formed by these capillaries were more commonly oval and had dimensions

approaching those observed in the control group of animals.

The efferent lymphatic vessels anastomosed with one another, forming plexuses that were

located in the same plane as the capillary network. The anastomoses between the efferent

vessels were well developed, with a diameter of 38.0 ± 2.0 μm (P < 0.001).

In the muscular layer, lymphatic capillaries formed a single-layered network. The loops of

the capillaries and the collecting vessels were oriented toward the mesenteric edge of the

intestinal wall. The lacunae formed by these vessels had a triangular shape. The contours of

the efferent vessels, now reduced in diameter, were smooth, and the distances between

valves in their lumens were elongated.

In the serous membrane, lymphatic capillaries formed small oval-shaped loops, whose

internal dimensions were increased. The lacunae had an irregular star-shaped form. The

efferent lymphatic vessels of the 1st, 2nd, and 3rd order, compared to earlier postoperative

periods, were reduced in diameter. The anastomoses between these vessels were fairly large

(4.0 ± 2.0 μm, P < 0.001), and some of them even exceeded the diameter of the main vessels.

One to six months after gastrectomy

, due to the proliferation of vessels through the

formation of numerous anastomoses and lateral finger-like and other protrusions, an

extensive network of lymphatic capillaries and vessels is formed. Under these conditions,

the vessels of the mucosal and submucosal layers — and less frequently, those of the serous

and subserous layers — noticeably lose their orderly arrangement and directional orientation.

A clearer orientation is retained by the larger second- and third-order vessels, which help

determine the direction of lymphatic outflow.

In the early stages following gastrectomy performed using the Billroth I method and its

modifications, pathomorphological changes of the small intestinal wall are observed in the

form of mucosal edema, deformation of villi and crypts (see Fig. 2, a, b).

Hypertrophy of individual mucosal villi is accompanied by a reduction in their overall

number per unit area. The surface epithelium of the villi contains numerous goblet cells, and

the crypts are shortened and dilated.

In the stroma of the villi and crypts, diffuse infiltration is observed, predominantly

lymphocytic in nature. The apical part of the cytoplasm in the columnar cells of many crypts

and some villi shows a strongly positive PAS reaction. In the hypertrophied villi, high

activity of alkaline phosphatase is noted in the apical parts of the cells and in the brush

border zone.

During this period, microstructural changes in the intestinal mucosa after gastrectomy using

the Billroth II method and its Hofmeister–Finsterer modifications are manifested by

pronounced edema and infiltration of the villous stroma by lymphocytes. A large number of

lymphocytes are found among the epithelial cells. Villi deformation, lymphocytic infiltration,

and destruction of some crypts are observed (see Fig. 2, b). The submucosal layer is

markedly sclerotic. Due to compression of the lymphatic vessels, phenomena of

lymphostasis occur, and the lacteals of the villi are also dilated. The lamina propria of the


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crypts and villi is infiltrated by lymphoid and plasma cells. Between the crypts, small areas

of fibrous tissue can be seen, which may replace isolated groups of crypts. In these areas,

villi are either absent or appear severely shortened.

In the muscular layer, dystrophic changes are observed, with small foci of round-cell

infiltration and dilated blood vessels.

At later stages after the operation (using the Billroth I method and its modifications), signs

of mucosal inflammation persist (edema, some hemodynamic disorders, as well as epithelial

destruction). However, during this time, an increase in the size of villi and crypts is noted,

the number of goblet cells decreases, the height of the columnar cells increases, and the

brush border becomes thickened and distinctly outlined, especially in the surface epithelium.

The submucosal layer is slightly edematous and shows focal infiltration by plasma cells. The

ganglion cells of the nerve plexuses located in the submucosa and muscular layer are

edematous, and their cytoplasm appears vacuolated.

After gastrectomy using the Hofmeister–Finsterer method, and especially the Polya–Reichel

method, atrophy of the small intestinal mucosa is observed. The villi become noticeably

shortened, and their tips become almost flat. Some villus tips appear deformed with club-

shaped swellings. Certain villi are fused together, mainly in the apical region. Between the

fused villi, peculiar pockets form that contain mucus in which neutral glycosaminoglycans

are detected. The number of goblet cells in the epithelium increases significantly, and they

become larger. Focal hyperemia of the vessels persists, while cellular infiltration decreases.

Conclusion:

Thus, the morphological remodeling of the lymphatic vessels in the intestinal

wall is compensatory in nature and is aimed at maintaining hemostasis and microcirculation,

as well as facilitating the transport of increased lymph production under conditions of

venous stasis and interstitial edema of the intestinal wall — a condition that develops

following acute trauma to the main vascular and neural structures of the stomach.

References

1.

Aminova G.G. On the issue of functional morphology of the roots of the lymphatic

systems.

Archives

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Anatomy

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Borodin Yu.I., Bikbulatov Z.T., and Kolesnikov S.I. Chronic venous stasis as a

factor in the morphological remodeling of the lymphatic network.

Archives of Anatomy

,

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Voronich M.V., Polozhinits M.N., and Ganich O.N. The impact of Billroth II

gastrectomy on the digestive function of the small intestine.

Herald of Surgery

, 1983, No. 1,

pp. 67–71.

4.

Vyrenkov Yu.E. Current issues in lymphology. In the book:

Current Issues in

Lymphology and Angiology

, Moscow, Medicina, 1981, pp. 5–10.

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Pestereva N.A. Ultrastructure of lymphatic capillaries in the wall of the small

intestine.

Archives of Anatomy

, 1981, Vol. 81, Issue 7, pp. 35–40.

References

Aminova G.G. On the issue of functional morphology of the roots of the lymphatic systems. Archives of Anatomy, 1972, Vol. 63, Issue 9, pp. 33–40.

ISSN 2414-9918, Modern Science, No. 9, Vol. I

Borodin Yu.I., Bikbulatov Z.T., and Kolesnikov S.I. Chronic venous stasis as a factor in the morphological remodeling of the lymphatic network. Archives of Anatomy, 1975, Vol. 68, Issue 1, pp. 102–107.

Voronich M.V., Polozhinits M.N., and Ganich O.N. The impact of Billroth II gastrectomy on the digestive function of the small intestine. Herald of Surgery, 1983, No. 1, pp. 67–71.

Vyrenkov Yu.E. Current issues in lymphology. In the book: Current Issues in Lymphology and Angiology, Moscow, Medicina, 1981, pp. 5–10.

Pestereva N.A. Ultrastructure of lymphatic capillaries in the wall of the small intestine. Archives of Anatomy, 1981, Vol. 81, Issue 7, pp. 35–40.