Introduction
The development of three-dimensional computed tomography bronchography and angiography (3-DCTBA) imaging brings convenience for thoracic surgeons to know the precise anatomical relationship among bronchi, pulmonary artery, and vein before pulmonary surgery [
1‐
3]. As increasing reports about the variations of pulmonary anatomy in 3-DCTBA have been published [
4‐
7], how to understand the complex and diverse variations becomes desirable.
In previous studies on pulmonary morphology, the objects are mainly human embryo specimens [
8‐
10], which brought direct evidence for the origins of some congenital anomalies and variations. Meanwhile, given the discrepancies of pulmonary morphology between embryo and adult, these researches still can't clarify the common variations that thoracic surgeons often meet during pulmonary surgery. Now accumulating mass of the 3-DCTBA data from adults make it possible to study these anatomical variations.
We chose the mediastinal lingular artery (MLA), one of the most common variations [
11,
12], as the study object, and analyzed the different patterns of bronchi and vessels in left upper lobe (LUL) by categorizing them into mediastinal (M-type) group and interlobar (IL-type) group. In this way, this study aims to explore the genesis of MLA and provide a perspective to understand pulmonary anatomical variations in left upper lobe influenced by MLA.
Discussion
Among all the variations in both lungs, the mediastinal lingular artery (MLA) may be the most common and distinguishable one which doesn’t parallel the accompanying bronchi at proximal [
15]. In our study, we choose MLA as layered strata to analyze the different patterns of bronchi and vessels between M-type and IL-type group. By discussing the distribution of patterns respectively, we try to provide a perspective to understand the genesis of MLA and its influence on pulmonary anatomy in left upper lobe (LUL).
The variations and aberrant branches of lung originate from the complex development of the embryo. According to DeMello’s study [
16], the formation of vascular tree contains two mechanisms: angiogenesis and vasculogenesis. Angiogenesis produces the proximal central trunks by branching of new vessels from preexisting ones, and vasculogenesis produces a distal capillary network by the development of blood lakes that transform to vessels. Thus, it is reasonable to speculate that the MLA originates from angiogenesis. For the development of human lung, the timeline is described as that airway emerges before pulmonary artery and vein appears afterward [
17,
18]. Hall confirmed that bronchus is necessary for pulmonary artery during the development stage, as smooth muscle from the airway makes up the innermost layers of pulmonary artery when it becomes mature [
19], whereas vasculature is dispensable for epithelial branching of bronchi at its embryonic development stage [
20,
21].
Combined with our results, the B
3 bronchial patterns seem to play an important part in the formation of MLA. Metzger et al. studied the early bronchial tree by examining chemically fixed lung tissue from mouse embryos using microscopy. They have revealed that bronchi branching in three geometrical modes: domain branching, planar bifurcation, and orthogonal bifurcation [
22]. These modes reasonably explain the different patterns of B
3. One of the reasons why the different patterns of B
3 are relevant to the probability of MLA, from our perspective, is that the apico-anterior type of B
3 leaves more space for lingular bronchus by the side of hilus, generating artery easily from left pulmonary trunk into lingular division. Another concept assumed by Onuki et al. [
23] that ‘the lung segments never continuously exist from the early stage of the embryonic period as units, but they are only simple units artificially named by their prevailing bronchial branching patterns’. They also found that the combination of anterior extension type of B
3 bronchus with the inter-lobar type (IL-type) of arterial branching was often observed, as well as the combination of apico-anterior extension type with the mediastinal type (M-type) [
7]. They speculated the location, which originally would be S
3 in IL-type, would become a part of S
4+5 in M-type after the whole axis of LUL rotates.
We also verified that the distribution of bronchial and vascular branching patterns in LUL between wM-type and pM-type has no significant difference. This implies that wM-type and pM-type may result from similar embryonic development.
Our layered testing results revealed that the distribution of PV type in LUD is distinct among the three different patterns of B
3 and between M-type and IL-type groups. As demonstrated in the 3-DCTBA, pulmonary vein lies at a distance from bronchus, suggesting that pulmonary vein, different from pulmonary artery which received muscle cells from bronchus, is influenced less by airway. However, Hall [
18] has used immunohistochemical techniques to study serial sections of human embryonic and fetal lungs. And his study indicated that veins ran midway between airways where the mesenchymal cell density was low. In other words, the bronchial pattern shapes the density of mesenchymal cells during embryonic stage which further influences the pattern of pulmonary vein. Interestingly, when excluded the influence from the patterns of B
3, the venous pattern of LUD is still affected by the MLA independently. Dejima et al. [
11] have concluded that MLA is associated with greater artery diameter and larger lingular division volume. This indicates that the lingular division in M-type group has more blood flow volume. Our study revealed that V cent type vein often appears in M-type group and V semi-cent type often appears in IL-type group. Whether the different venous patterns reveal not only the variations of pulmonary vein in LUD, but also the blood flow distribution in LUL? This relationship between different branching patterns of PV and the blood flow distribution in LUL needs to be investigated by precise data and appropriate analytical methods.
As the apicoposterior + anterior artery (A
1+2 + A
3) of LUL is characterized by its greatest variability, we used the classification proposed by Boyden and Hartman [
24] in 1946 to explore whether these subtypes have a significant influence on the genesis of MLA. Our study revealed that the distribution of these artery subtypes had no difference between M-type and IL-type groups, indicating that the pattern of pulmonary artery in LUD is irrelevant with the generation of MLA. In previous research or anatomical atlas [
24‐
26], lingular bronchi are generally divided into B4 and B5. However, based on our observation, 25.99% of lingular bronchi belong to miscellaneous type which means B
4 and B
5 are not independent. The different lingular bronchial patterns seem to have little influence on the formation of MLA as there is no significant difference in lingular bronchial patterns between M-type and IL-type groups. Besides, inspired by Dejima’s study about the blood flow of lingular division in M-type group [
11], we also counted the ramies of independent intrasegmental lingular vein, but there is no distinction between M-type and IL-type group even though the number in M-type seems to exceed that in IL-type.
This present study has possible limitations. First, the relation of bronchus and vessels demonstrated by 3-DCTBA may reverse causation, or even be interpreted as the false causation, because the patterns of bronchi and vessels in M-type group can’t certify embryonic development directly. Second, the classifications of bronchi and pulmonary vessels are empirical which may not reflect all the differences objectively. Furthermore, all the 3-DCTBA digital data come from patients undergoing pulmonary surgery, which may introduce selection bias. However, we carried a comprehensive comparison in patterns of bronchi and pulmonary vessels between M-type and IL-type group with a large number of cases, which illustrated the characteristics of pulmonary anatomy in LUL with or without MLA.
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