Authors

  • Д.Я. Хожиев
    кандидат медицинских наук, доцент, заведующий кафедрой анатомии и клинической анатомии Термезского филиала Ташкентской медицинской академии, Узбекистан
  • Т.В. Татун
    магистр педагогических наук, ассистент кафедры нормальной анатомии Гродненского Государственного медицинского университета, Беларусь
  • С. В. Аплевич,
    врач, заведующий кабинетом рентгеновской компьютерной диагностики УЗ «Гродненская университетская клиника», Беларусь
  • К. П. Астапенко,
    врач кабинета рентгеновской компьютерной диагностики УЗ «Гродненская университетская клиника», Беларусь

DOI:

https://doi.org/10.71337/inlibrary.uz.mpttp.76354

Keywords:

бронхиальное дерево врожденная аномалия трахеи трахеальный бронх компьютерная реконструкции КТ-изображений.

Abstract

Представлен клинический случай наличия добавочного бронха, отходящего из латеральной стенки трахеи, направленного к верхней доле легкого и участвующего в ее вентиляции. Установлено наличие частичного аномального дренажа легочных вен, дефект межпредсердной перегородки и гипоплазией правой подключичной вены. Рассмотрены рентгенологические особенности строения бронхиального дерева.


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УДК 616-007-053.1

АНАТОМИЧЕСКИЕ ОСОБЕННОСТИ ТРАХЕАЛЬНОГО БРОНХА И

ЧАСТИЧНЫЙ АНОМАЛЬНЫЙ ДРЕНАЖ ЛЕГОЧНЫХ ВЕН

(клинический случай)

Д.Я. Хожиев,

кандидат медицинских наук, доцент, заведующий

кафедрой анатомии и клинической анатомии Термезского филиала

Ташкентской медицинской академии, Узбекистан

Т.В. Татун,

магистр педагогических наук, ассистент кафедры нормальной

анатомии Гродненского Государственного медицинского университета,

Беларусь

С. В.

Аплевич,

врач, заведующий кабинетом рентгеновской компьютерной

диагностики УЗ «Гродненская университетская клиника», Беларусь

К. П. Астапенко,

врач кабинета рентгеновской компьютерной диагностики

УЗ «Гродненская университетская клиника», Беларусь

Аннотация:

Представлен клинический случай наличия добавочного бронха,

отходящего из латеральной стенки трахеи, направленного к верхней доле легкого
и участвующего в ее вентиляции. Установлено наличие частичного аномального
дренажа легочных вен, дефект межпредсердной перегородки и гипоплазией
правой подключичной вены. Рассмотрены рентгенологические особенности
строения бронхиального дерева.


Ключевые слова:

бронхиальное дерево, врожденная аномалия трахеи,

трахеальный

бронх,

компьютерная

томография,

мультипланарные

реконструкции КТ-изображений.

УДК 616-007-053.1

ANATOMICAL FEATURES OF THE TRACHEAL BRONCHUS AND

PARTIAL ANOMALOUS DRAINAGE OF THE PULMONARY VEINS:

A

Case Report

Khojiev DY

1

, Tatun TV

2

, Astapenka KP

3

, Aplevich SV

4


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1 Department of Anatomy and clinical anatomy, Termez branch of the Tashkent

Medical

Academy, Uzbekistan

2 Department of Normal Anatomy, Grodno State Medical University, Belarus

3,4 Department of X-ray computer diagnostics, Grodno University Clinic, Belarus

Сorresponding author: Khojiev DY, Associate Professor, 132000, Termiz city,

Islam Karimov

street 64 – House, e-mail dkhojiev@gmail.com

Abstract:

A clinical case of an anomaly in the development of the bronchial tree is

described. A case is characterized by the presence of an additional bronchial branch,
directed to the upper lobe of the lung and participating in its ventilation, and associated
with a partial anomalous pulmonary venous drainage, with an atrial septal defect and
hypoplasia of the right subclavian vein. Morphometric, topographic, and X-ray
anatomical characteristics of the bronchial tree and lung parenchyma were established.

Keywords:

bronchial tree, congenital tracheal anomaly, tracheal bronchus, partial

anomalous pulmonary venous drainage computed tomography, multiplanar
reconstructions of CT images.

Introduction

Tracheal bronchus is a rare congenital anomaly of the bronchial tree, occurring in

1% of the world population, characterized by the presence of a bronchial branch
extending from the lateral wall of the trachea, directed to the upper lobe of the lung
and participating in its ventilation. Usually, the accessory bronchial branch is located
on the right side of the trachea, at the level of the carina or 2 cm above it, but in other
cases, tracheal bronchi can arise from the cricoid cartilage [2].

The tracheal bronchus in most cases is located on the border of the middle and distal

thirds of the right side wall of the trachea, is more common in males and may be
associated with stenosis of the right main bronchus [3].

In numerous studies conducted among children, the tracheal bronchus was present

in 0.9–3%, in most cases arising from the right side wall. The prevalence of the right-
sided accessory bronchus of the trachea ranged from 0.1 to 2%, and the prevalence of
the left-sided bronchus was from 0.3 to 1% [6].


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The reasons for the development of the tracheal bronchus can be local disorders of

morphogenesis, the result of the reposition of a previously developed bronchus, or
combined with various dysontogenesis. Some researchers argue that this anomaly may
be associated with other congenital anomalies such as Down syndrome,
tracheoesophageal fistulas, esophageal, larynx, and duodenal atresia, spinal fusion
defects, congenital heart defects, and pulmonary hypoplasia [6]. In other cases, a rare
congenital anomaly of the bronchial tree can be associated with pathologies of
congenital heart diseases (valvular heart disease, tetralogy of Fallot, and aortic
coarctation) stenosis of the bilateral pulmonary arteries, stenosis or hypoplasia of the
main bronchus, anomalous pulmonary venous connection, stenosis of the trachea [7].

There are several classifications of this rare pathological condition. According to

one classification, there are three types of anatomical location of the tracheal bronchi:
type I - the tracheal bronchus is more than 2 cm away from the the carina and there is
a distal narrowing of the trachea; type II - the tracheal bronchus is more than 2 cm from
the the carina, but there is no distal narrowing of the trachea; type III - the tracheal
bronchus is 2 cm below the level of the the carina [4].

According to another classification, the tracheal bronchus is divided into three

types: type I - the tracheal bronchus is a bronchial diverticulum and its diameter is
almost equal to the diameter of the trachea; located above the carina (the bifurcation of
the trachea) ; type II - the bronchus begins above the carina (the bifurcation of the
trachea) and ventilates the upper lobe of the lung; and type III - the tracheal bronchus
is fully developed and located at the level the carina (the bifurcation of the trachea)
[1,6].

In most cases, the tracheal bronchus is discovered by chance, more often they are

asymptomatic, but sometimes it can be manifested by cough, chronic bronchitis,
recurrent right-sided pneumonia.

Partial anomalous pulmonary venous drainage is characterized by the absence of

connection of one or more veins with the left atrium and drainage of the pulmonary
veins into the right atrium or vena cava, which accounts for 0.3% of all congenital heart
defects. In 25% of cases, it is associated with an atrial or ventricular septal defect and
anomalies in the structure of the trachea and bronchial tree.



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Case presentation

We observed a 40-year-old man, who underwent multispiral computed tomography

(MSCT) of the thoracic cavity in 2023 at the University Clinic. The CT images looked
as follows: an accessory (tracheal) bronchus was visualized at the level of the fifth
thoracic vertebra, 22 mm above the level of the carina (tracheal bifurcation) [Figure 1:
computed tomography images]. It independently departed from the lateral wall of the
trachea on the right, went to the upper lobe of the right lung and participated in its
ventilation. Its diameter was 8 mm, length 25 - mm. In the parenchyma of the upper
lobe of the right lung, it was divided into two branches:

the anterior branch

, 16 mm

long and 3 mm in diameter, which divided dichotomously and occupied the
parenchyma of the anterior-apical segment of the lung parenchyma, and

the posterior

branch

, 10 mm long and 5 mm in diameter, which also divided dichotomously and

occupied the parenchyma of the posterior-apical segment of the lung parenchyma.

Figure 1 - an accessory (tracheal) bronchus.

CT scan: a - an axial chest CT image with lung window, b - coronal chest CT image

with lung window.


The bronchial tree looked like this: two main bronchi departed from the trachea,

the right one was narrowed, its diameter was 8 mm and 31 mm long, the left main

trache

al

bronchus

trachea

l bronchus


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bronchus was wider with a diameter of 11 mm and a length of 48 mm. [Figure 2:
computed tomography images].

Figure 2.CT scan: - an axial chest CT image with lung

window.

At the at the hilum of the right lung, the right main bronchus was divided into three

lobar bronchi: upper, middle and lower, while the oblique interlobar fissure of the right
lung was within normal, and the horizontal interlobar fissure was incomplete, dividing
the lung parenchyma into 1/3 of the anterior and lateral sections of the lung. There was
a change in the structure and division of superior lobar bronchus. The upper right lobar
bronchus was 4 mm wide, located lower than usual at the level of the middle third of
the div of the seventh thoracic vertebra and divided only into two segmental bronchi:
anterior and posterior, corresponded to normal third-order segmental bronchi.

According to the anatomical structure of the bronchial tree, the right upper lobe

bronchus is divided into three segmental bronchi: apical, posterior and anterior, located
in the upper lobe of the lung parenchyma. In our case, the accessory tracheal bronchus
was defined as an apical segmental bronchus of the third order, which was directed to
the upper lobe of the right lung in the apical segment.The pulmonary parenchyma was
without additional formations and inflammatory changes.

right

main

left main

bronchus


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The clinical case was associated with partial congenital anomalous drainage of the

right upper and lower pulmonary veins into the superior vena cava and an operated
atrial septal defect.

The anatomical features of the blood supply of the segments of the anomalous

tracheal bronchus were as follows: the right pulmonary veins merged into segmental
trunks with diameters of 12 mm (anterior) and 8 mm (posterior), and then merged into
a common trunk with a cross-section of 17 mm. Blood drained into the superior vena
cava instead of the left atrium, which indicates a false "scimitar" syndrome (partial
anomalous drainage of the pulmonary veins). Mixing of blood occurs at the site of
drainage of the right pulmonary veins and the superior vena cava. Oxygenated blood,
entering the lumen of the superior vena cava, with a mixture of deoxygenated blood,
flows into the right atrium, creating difficulty in the work of the heart and pulmonary
vessels in the form of hypertension and hypoxia of the internal organs.

Hypoplasia of the right subclavian vein was detected: the diameter was narrowed to

3 mm in the area 10 mm distal to the intersection of the first rib and was located 10
mm before it entered the right brachiocephalic vein.

Conclusion

As a result of the study, an anatomical picture of the structure of the bronchial tree

with the presence of the right tracheal bronchus was revealed. This rare congenital
anomaly was associated with stenosis of the right main bronchus, hypoplasia of the
right subclavian vein, incomplete right horizontal interlobar fissure, corresponded to
type II (the bronchus began 22 mm above the bifurcation and ventilated the upper lobe
of the lung), partial congenital anomalous drainage of the right upper and lower
pulmonary veins into the superior vena cava and an operated atrial septal defect. Such
an anomaly was revealed for the first time in the University Clinic [5]. The case
described expands and complements the understanding of the morphometric,
topographic and radiological characteristics of a rare congenital pathology of the
bronchial tree.

Conflict of interest

None.


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Acknowledgement

None.

References

1.

Conacher ID. Implications of tracheal bronchus for adult anaesthetic practice // Br J
Anaesth. – 2000. – Vol. 85. – P. 317-337.

2.

DelPizzo KR, Tracheal bronchus in a 10-month-old patient for thoracoscopic
resection of congenital cystic adenomatoid malformation / DelPizzo KR, Joffe DC,
Finkel JC. // J PediatrAnesth. – 2006. – Vol. 16. – P. 997-1005.

3.

Doolıttle AM, Tracheal bronchus: classification,endoscopic analysis, and airway
management / Doolıttle AM, Maır EA // J. OtolaryngolHead Neck Surg. – 2002. –
Vol. 3.– P.240-243.

4.

Giral T, Ventilation unipulmonaire chez unepatienteprésentantune trifurcation
bronchique / Giral T, Marandon J-Y, Fischler M. // J. Ann FrAnesthRéanim. –2014. –
Vol. 33.– P.272-276.

5.

Khojiev DY, Morphological features of the small intestine: A Case Report / D. Y.
Khojiev, T. V. Tatun, K. P. Astapenka, D. J. Khalimova // Journal of Advanced
Zoology. – 2023. – Vol. 44 (S2). – Р. 5379-83.

6.

Lawrence DA, The wonderful world of the windpipe: a review of central airway
anatomy and pathology / Lawrence DA, Branson B, Oliva I, Rubinowitz A. //J
Canadian Association of Radiologists. – 2015. – Vol. 66.– P.30-43.



References

Conacher ID. Implications of tracheal bronchus for adult anaesthetic practice // Br J Anaesth. – 2000. – Vol. 85. – P. 317-337.

DelPizzo KR, Tracheal bronchus in a 10-month-old patient for thoracoscopic resection of congenital cystic adenomatoid malformation / DelPizzo KR, Joffe DC, Finkel JC. // J PediatrAnesth. – 2006. – Vol. 16. – P. 997-1005.

Doolıttle AM, Tracheal bronchus: classification,endoscopic analysis, and airway management / Doolıttle AM, Maır EA // J. OtolaryngolHead Neck Surg. – 2002. – Vol. 3.– P.240-243.

Giral T, Ventilation unipulmonaire chez unepatienteprésentantune trifurcation bronchique / Giral T, Marandon J-Y, Fischler M. // J. Ann FrAnesthRéanim. –2014. – Vol. 33.– P.272-276.

Khojiev DY, Morphological features of the small intestine: A Case Report / D. Y. Khojiev, T. V. Tatun, K. P. Astapenka, D. J. Khalimova // Journal of Advanced Zoology. – 2023. – Vol. 44 (S2). – Р. 5379-83.

Lawrence DA, The wonderful world of the windpipe: a review of central airway anatomy and pathology / Lawrence DA, Branson B, Oliva I, Rubinowitz A. //J Canadian Association of Radiologists. – 2015. – Vol. 66.– P.30-43.