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Kidney surface development in human fetuses: study applied to radiological diagnosis

ABSTRACT

Objective:

To evaluate the anatomical aspects of the kidney surface in human fetuses during the second gestational trimester.

Material and Methods:

We studied 108 kidneys obtained from 54 human fetuses (29 males and 25 females). The kidney was dissected and the number of clefts was counted. The renal volume was also assessed. To compare the quantitative data in both sexes, the Students-t-test was used (p < 0.05). Simple linear correlations were calculated for all kidney measurements, according to fetal age. Statistical analysis was performed with the R program (Version 3.5.1).

Results:

The fetuses ranged in age between 11.4 to 23 weeks post-conception. The renal volume of the right kidney ranged from 0.09 to 2.397 cm (mean=0.8479) and the renal volume of the left kidney ranged from 0.07 to 2.416 cm (mean=0.8036). The mean number of renal clefts in fetuses studied was 15.25 (7 to 28). There was no statistical significant difference in renal clefts between the sides either in males (p = 0.646) or in females (p = 0.698). Also, there was no significant difference in the mean number of renal clefts between male and female fetuses in right kidney (p = 0.948) and in left kidney (p = 0.939).

Conclusions:

The number of renal clefts has a great variation, weak correlation and no tendency to decrease during the 2nd gestational trimester. The number of clefts in right kidney of total sample and female fetuses has a significant development with age.

Keywords:
Kidney; Branchio-Oto-Renal Syndrome; Embryology

INTRODUCTION

The 2nd gestational trimester is very important for the embryonic development of the kidneys, renal pelvis, ureter and bladder (11 Keith L. Moore BA MSc PhD DSc FIAC FRSM FAAA, T. V. N. Persaud MD PhD DSc FRCPath (Lond.). The Developing Human: Clinically Oriented Embryology (DEVELOPING HUMAN (MOORE)) 7th Edición, 22 Short KM, Smyth IM. The contribution of branching morphogenesis to kidney development and disease. Nat Rev Nephrol. 2016; 12:754-767.). An important branching of the ureteric bud occurs between the 5th and 14th weeks post conception, leading to formation of the major and minor renal calyces, renal pelvis and collecting tubules (33 Stephens FD, Smith ED, Hutson JM. Morphology and embryology of the kidney. In Congenital anomalies of the kidney, urinary and genital tracts. London: Martin Dunitz. 2002; chapter 11: pp. 283-92., 44 Ishiyama H, Ishikawa A, Kitazawa H, Fujii S, Matsubayashi J, Yamada S, et al. Branching morphogenesis of the urinary collecting system in the human embryonic metanephros. PLoS One. 2018; 13:e0203623.). This branching will be important to the renal lobulations development.

The surface of the fetal kidney is divided by a number of clefts into lobes and lobules. Fetal kidney lobes (clefts) are fine, linear demarcations indenting the renal surface, separating normal lobes, consisting of a central pyramid, and surrounding cortex (55 Hodson J. The lobar structure of the kidney. Br J Urol. 1972; 44:246-61., 66 Blake J, Rosenblum ND. Renal branching morphogenesis: morphogenetic and signaling mechanisms. Semin Cell Dev Biol. 2014; 36:2-12.). The interlobular boundary lines are apparent as grooves on the surface of the fetal kidney but are rarely visible in the mature kidney (77 Patriquin H, Lefaivre JF, Lafortune M, Russo P, Boisvert J. Fetal lobation. An anatomo-ultrasonographic correlation. J Ultrasound Med. 1990; 9:191-7.). The persistent fetal kidney lobulation is a rare anatomic variant and can mimic a renal neoplasm leading to a wrong radiological diagnosis. This condition is denominated as renal pseudotumors (88 Bhatt S, MacLennan G, Dogra V. Renal pseudotumors. AJR Am J Roentgenol. 2007; 188:1380-7.).

Studies of the renal clefts development in human fetuses are rare. We hypothesized that the renal clefts are observed during the 2nd gestational trimester without differences between the genders and sides and showing a lower incidence at the end of this period. The objective of this work is to evaluate the anatomical aspects of the kidney surface in human fetuses during the 2nd gestational trimester.

MATERIALS AND METHODS

The study was approved according to the ethical standards of the hospital's institutional committee on experimentation with human beings (IRB: 4.088.773, CAAE:31780419.0.0000.5259).

We studied 108 kidneys obtained from 54 human fetuses (29 males and 25 females) ranging in age from 11.4 to 23 weeks post-conception (WPC). The fetuses were macroscopically well preserved, with no signs of malformation, and the stillbirth was due to hypoxia. Gestational age was determined at WPC according to the length of the foot. Currently, this criterion is considered the most acceptable parameter for estimating gestational age (99 Hern WM. Correlation of fetal age and measurements between 10 and 26 weeks of gestation. Obstet Gynecol. 1984; 63:26-32.1111 Platt LD, Medearis AL, DeVore GR, Horenstein JM, Carlson DE, Brar HS. Fetal foot length: relationship to menstrual age and fetal measurements in the second trimester. Obstet Gynecol. 1988; 71:526-31.). The fetuses were also evaluated regarding total length (TL), crown-rump length (CRL) and body weight immediately before dissection with the aid of a digital pachymeter. The same observer made all the measurements (1212 Tello C, Liebmann J, Potash SD, Cohen H, Ritch R. Measurement of ultrasound biomicroscopy images: intraobserver and interobserver reliability. Invest Ophthalmol Vis Sci. 1994; 35:3549-52., 1313 Vieiralves RR, Sampaio FJB, Favorito LA. Urethral and bladder development during the 2nd gestational trimester applied to the urinary continence mechanism: translational study in human female fetuses with neural tube defects. Int Urogynecol J. 2021; 32:647-652.). The fetuses were donated by the hospital's obstetrics department. All data were collected from July 2018 to November 2021.

Using a standardized technique, the fetuses were carefully dissected with extraction of the kidneys and ureters with the aid of a stereoscopic lens with 16/25X magnification. All fetuses were dissected under identical conditions by the same researcher, who has practical experience in microsurgery. After kidney dissection, we evaluated the following measurements with the aid of a digital pachymeter: renal length, width of the superior pole, width of the inferior pole, and renal thickness (Figure-1). The data were expressed in centimeters. The fetal renal volume was calculated using the ellipsoid formula (1414 Sampaio FJ. Theoretical kidney volume versus real kidney volume: comparative evaluation in fetuses. Surg Radiol Anat. 1995; 17:71-5.): Renal volume (RV) = [renal length x renal thickness x renal width (lower pole + upper pole)/2] x 0.523.

Figure 1
Renal clefts and kidney measurements.

A) The figure shows some units of our sample after the fetal kidney dissection; B) Fetal kidney of a male fetus with 16 weeks post-conception in anterior position, we marked each cleft with a green color pen; C) Schematic drawing of kidney measurements: Renal length, lower pole width, hilar width and upper pole width and D) The figure shows the measurement of the upper pole width with the aid of a digital pachymeter.

After the measurements the kidney was dissected in our laboratory with the aid of a microscope (Zeiss Discovery V8 microscope with stereoscopic lens with 16/25X magnification) and the number of clefts was counted (Figure-1). We observed the fetal kidneys in anterior position, lateral position, and posterior position and to facilitate the clefts number identification we marked each cleft with a color pen (Figure-1).

Statistical Analysis

All parameters were statistically processed and graphically described. To compare the quantitative data in both sexes, the students-t-test was used (p < 0.05). Simple linear correlations (where r² values less than 0.4 reflect very weak correlation, r² between 0.4 and 0.7 reflect moderate correlation and r² greater than 0.7 indicate strong correlation) were calculated for all kidney measurements, according to fetal age. The statistical analysis was performed with the R program (Version 3.5.1).

RESULTS

The fetuses ranged in age between 11.4 to 23 WPC, weighted between 60 and 780g, and had crown-rump length between 7.3 and 22.2 cm. The mean number of renal clefts in fetuses studied was 15.25 (7 to 28). The statistical analysis of all kidneys biometric parameters measurements is reported in Table-1.

Table 1
The table presents the statistical analysis of the main fetal parameters and the renal clefts in 54 fetuses studied.

There was no statistically significant difference in renal clefts between the sides either in males (p = 0.646) or in females (p = 0.698). Also, there was no significant difference in the mean number of renal clefts between male and female fetuses in right kidney (p = 0.948) and in left kidney (p = 0.939). The renal volume of the right kidney ranged from 0.09 to 2.397 cm (mean = 0.8479) and the renal volume of the left Kidney ranged from 0.07 to 2.416 cm (mean = 0.8036). The analysis of the fetal kidney volume showed no significant statistical difference between side and sex comparisons (Volume of right kidney x left kidney (males and females): p = 0.057; Volume of right kidney x left kidney (males): p = 0.067; Volume of right kidney x left kidney (females): p = 0.333; Males x females (volume of right kidney): p = 0.381 and Males x females (volume of left kidney): p = 0.359).

The linear correlation was performed to enable analysis of morphological data at different gestational ages. Results for male fetuses’ renal volume (Right kidney: r = 0.763, p < 0.001 and Left kidney: r = 0.755, p < 0.001) and female fetuses’ renal volume (Right kidney: r = 0.698, p < 0.001 and Left kidney: r = 0.751, p < 0.001), indicated that the renal volume increased significantly during the fetal period studied in males and females fetuses.

The linear correlation of renal lobes was performed to enable analysis of morphological data at different gestational ages. The linear correlation of the 54 fetuses renal clefts is shown in Figure-2. The linear correlation indicated that the fetal renal lobes number increased with age both in total sample, female and male fetuses, but the differences were not statistically significant, and the correlation was weak. The exception was the renal right clefts in total sample and female fetuses that has a significant development with age.

Figure 2
Linear regression analysis comparing the correlation of the renal clefts and fetal age (WPC).

DISCUSSION

In the beginning of the 5th week of development, the ureteral buds originate at the distal portion of the mesonephric ducts and merges with the metanephrogenic blastema (1515 Glassberg KI. Normal and abnormal development of the kidney: a clinician's interpretation of current knowledge. J Urol. 2002; 167:2339-50; discussion 2350-1., 1616 Thomas FMD, Rickwood, AMK, Duffy PG. Essentials of paediatric urology. 1st ed. London: Martin Dunitz Ltda. 2002; pp. 283-359.). In this paper we studied fetuses of the 2nd trimester of gestation. At this age, the kidneys are expected to have reached their final position and from then on they will only develop in size, representing an ideal moment for this study. In our sample we observed that the renal parenchymal volume had a strong and positive correlation with fetal age during the 2nd gestational trimester.

The branching of the ureteral buds will determine the pyelocaliceal pattern and the corresponding renal lobules (22 Short KM, Smyth IM. The contribution of branching morphogenesis to kidney development and disease. Nat Rev Nephrol. 2016; 12:754-767., 1717 Speller AM, Moffat DB. Tubulo-vascular relationships in the developing kidney. J Anat. 1977; 123 (Pt 2): 487-500., 1818 Pole RJ, Qi BQ, Beasley SW. Patterns of apoptosis during degeneration of the pronephros and mesonephros. J Urol. 2002; 167:269-71.). The kidney fetal lobe is made up of medullary pyramid surrounded by cortex, separated by interlobar grooves and drained by single calyx. The kidney interlobar grooves disappear during the third gestational trimester (55 Hodson J. The lobar structure of the kidney. Br J Urol. 1972; 44:246-61.).

The persistence of kidney fetal clefts is a rare anatomic variant characterized by fine, linear demarcations indenting the renal surface between normal renal lobes and consisting of normal central pyramids and surrounding cortex which are mistaken as tumor and can lead a difficulty radiological diagnosis. This condition is called renal pseudotumor (88 Bhatt S, MacLennan G, Dogra V. Renal pseudotumors. AJR Am J Roentgenol. 2007; 188:1380-7., 1919 Felson B, Moskowitz M. Renal pseudotumors: the regenerated nodule and other lumps, bumps, and dromedary humps. Am J Roentgenol Radium Ther Nucl Med. 1969; 107:720-9.). Renal pseudotumor is a term that include persistent fetal lobulation, hypertrophy of Bertin columns and dromedary humps (88 Bhatt S, MacLennan G, Dogra V. Renal pseudotumors. AJR Am J Roentgenol. 2007; 188:1380-7., 1919 Felson B, Moskowitz M. Renal pseudotumors: the regenerated nodule and other lumps, bumps, and dromedary humps. Am J Roentgenol Radium Ther Nucl Med. 1969; 107:720-9.).

Radiological confirmation of persistent fetal lobulation of kidney can be made by documenting the presence of renal pyramid in the bulge bounded by septa of Bertin on either side (2020 Yeh HC. Some misconceptions and pitfalls in ultrasonography. Ultrasound Q. 2001; 17:129-55.). Radiologist can make potential errors during image interpretation of persistent fetal lobulation especially on conventional and power Doppler ultrasound scan and to reach a secure diagnosis, a CT or MRI should be done (77 Patriquin H, Lefaivre JF, Lafortune M, Russo P, Boisvert J. Fetal lobation. An anatomo-ultrasonographic correlation. J Ultrasound Med. 1990; 9:191-7.).

The fetal kidney grooves become invisible during the third trimester resulting in smooth renal surface (55 Hodson J. The lobar structure of the kidney. Br J Urol. 1972; 44:246-61., 2121 Zalel Y, Lotan D, Achiron R, Mashiach S, Gamzu R. The early development of the fetal kidney-an in utero sonographic evaluation between 13 and 22 weeks’ gestation. Prenat Diagn. 2002; 22:962-5.). This paper presents the first normative parameters of fetal renal clefts development during the 2nd gestational trimester, and we observed that the renal clefts number increased with age, however the correlation was weak in the fetal period analyzed, except in the right side of total sample and in the right side of female fetuses where the number of clefts has a significant development with age. We observed that the differences of the development of renal clefts number were not statistically significant between genders and side.

Renal clefts showing no tendency to decrease during the 2nd gestational trimester and this finding may justify the persistence of renal lobulations during the 3rd gestational trimester and after birth, however the absence of 3rd gestational trimester fetuses in our sample to determine the moment when the lobulations begin to disappear is an important limitation of this work.

CONCLUSIONS

The number of renal clefts has a great variation, weak correlation, and no tendency to decrease during the 2nd gestational trimester. The number of clefts in right kidney of total sample and female fetuses has a significant development with age.

ACKNOWLEDGMENTS

An earlier version of this paper has been presented in the European Urology Congress according to the following link: https://resource-centre.uroweb.org/resource-centre/eau19/189800/Poster?

This work was supported by the Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq-Brasil) and the Fundação de Amparo à Pesquisa do Estado do Rio de Janeiro (FAPERJ).

REFERENCES

  • 1
    Keith L. Moore BA MSc PhD DSc FIAC FRSM FAAA, T. V. N. Persaud MD PhD DSc FRCPath (Lond.). The Developing Human: Clinically Oriented Embryology (DEVELOPING HUMAN (MOORE)) 7th Edición
  • 2
    Short KM, Smyth IM. The contribution of branching morphogenesis to kidney development and disease. Nat Rev Nephrol. 2016; 12:754-767.
  • 3
    Stephens FD, Smith ED, Hutson JM. Morphology and embryology of the kidney. In Congenital anomalies of the kidney, urinary and genital tracts. London: Martin Dunitz. 2002; chapter 11: pp. 283-92.
  • 4
    Ishiyama H, Ishikawa A, Kitazawa H, Fujii S, Matsubayashi J, Yamada S, et al. Branching morphogenesis of the urinary collecting system in the human embryonic metanephros. PLoS One. 2018; 13:e0203623.
  • 5
    Hodson J. The lobar structure of the kidney. Br J Urol. 1972; 44:246-61.
  • 6
    Blake J, Rosenblum ND. Renal branching morphogenesis: morphogenetic and signaling mechanisms. Semin Cell Dev Biol. 2014; 36:2-12.
  • 7
    Patriquin H, Lefaivre JF, Lafortune M, Russo P, Boisvert J. Fetal lobation. An anatomo-ultrasonographic correlation. J Ultrasound Med. 1990; 9:191-7.
  • 8
    Bhatt S, MacLennan G, Dogra V. Renal pseudotumors. AJR Am J Roentgenol. 2007; 188:1380-7.
  • 9
    Hern WM. Correlation of fetal age and measurements between 10 and 26 weeks of gestation. Obstet Gynecol. 1984; 63:26-32.
  • 10
    Mercer BM, Sklar S, Shariatmadar A, Gillieson MS, D’Alton ME. Fetal foot length as a predictor of gestational age. Am J Obstet Gynecol. 1987; 156:350-5.
  • 11
    Platt LD, Medearis AL, DeVore GR, Horenstein JM, Carlson DE, Brar HS. Fetal foot length: relationship to menstrual age and fetal measurements in the second trimester. Obstet Gynecol. 1988; 71:526-31.
  • 12
    Tello C, Liebmann J, Potash SD, Cohen H, Ritch R. Measurement of ultrasound biomicroscopy images: intraobserver and interobserver reliability. Invest Ophthalmol Vis Sci. 1994; 35:3549-52.
  • 13
    Vieiralves RR, Sampaio FJB, Favorito LA. Urethral and bladder development during the 2nd gestational trimester applied to the urinary continence mechanism: translational study in human female fetuses with neural tube defects. Int Urogynecol J. 2021; 32:647-652.
  • 14
    Sampaio FJ. Theoretical kidney volume versus real kidney volume: comparative evaluation in fetuses. Surg Radiol Anat. 1995; 17:71-5.
  • 15
    Glassberg KI. Normal and abnormal development of the kidney: a clinician's interpretation of current knowledge. J Urol. 2002; 167:2339-50; discussion 2350-1.
  • 16
    Thomas FMD, Rickwood, AMK, Duffy PG. Essentials of paediatric urology. 1st ed. London: Martin Dunitz Ltda. 2002; pp. 283-359.
  • 17
    Speller AM, Moffat DB. Tubulo-vascular relationships in the developing kidney. J Anat. 1977; 123 (Pt 2): 487-500.
  • 18
    Pole RJ, Qi BQ, Beasley SW. Patterns of apoptosis during degeneration of the pronephros and mesonephros. J Urol. 2002; 167:269-71.
  • 19
    Felson B, Moskowitz M. Renal pseudotumors: the regenerated nodule and other lumps, bumps, and dromedary humps. Am J Roentgenol Radium Ther Nucl Med. 1969; 107:720-9.
  • 20
    Yeh HC. Some misconceptions and pitfalls in ultrasonography. Ultrasound Q. 2001; 17:129-55.
  • 21
    Zalel Y, Lotan D, Achiron R, Mashiach S, Gamzu R. The early development of the fetal kidney-an in utero sonographic evaluation between 13 and 22 weeks’ gestation. Prenat Diagn. 2002; 22:962-5.

Publication Dates

  • Publication in this collection
    11 Nov 2022
  • Date of issue
    Nov-Dec 2022

History

  • Received
    01 July 2022
  • Accepted
    15 July 2022
  • Published
    20 Aug 2022
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