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Histogenesis of the Human Foetal Kidney in Mid-gestational Period: A Cross-sectional Study |
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SUVARNA ANIRUDHA GULANIKAR, GAUTAM AJIT SHROFF, AISHWARYA ANIRUDHA GULANIKAR 1. Associate Professor, Department of Anatomy, R K Damani Medical College, SRIMS, Chh. Sambhajinagar, Maharashtra, India. 2. Professor and Head, Department of Anatomy, MGM Medical College and Hospital, Chh. Sambhajinagar, Maharashtra, India. 3. Medical Officer, Department of Medicine, R K Damani Medical College, SRIMS, Chh. Sambhajinagar, Maharashtra, India. |
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Correspondence Address : Suvarna Anirudha Gulanikar, 7/A, Hiranya Nagar SO., Garkheda Parisar, Near Ulka Nagari, Chh. Sambhajinagar-431009, Maharashtra, India. E-mail: suvarnagulanikar@gmail.com |
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| ABSTRACT |  | ||||||
: Introduction: The histological maturation of the human foetal kidney is a critical determinant of prenatal renal health and provides a primary baseline for diagnosing Congenital Anomalies of the Kidney and Urinary Tract (CAKUT). While contemporary molecular insights have expanded current understanding of renal development, detailed morphological benchmarks for the mid-gestational period remain essential for clinical pathology and prenatal imaging. Aim: To delineate the sequential histogenesis milestones of the human kidney during the crucial 14- to 28-week gestational period. Materials and Methods: A cross-sectional observational histological study was conducted on 30 human foetuses (20 male, 10 female) ranging from 14 to 28 weeks of gestation at Department of Anatomy, MGM Medical College and Hospital, Chhatrapati Sambhajinagar. The study was conducted over a duration of two years, (January 2011- February 2013) to ensure the collection of adequate specimens for research. Gestational age was determined using Crown-Rump Length (CRL) and foot length. Renal specimens were fixed in 10% formalin for 24 hours, embedded in paraffin and serially sectioned at 7 μm thickness. Sections were stained with Haematoxylin and Eosin (H&E) and Masson’s Trichrome. Histological sections of foetal kidneys were examined under a light microscope at 4×, 10×, 40× and 100x magnifications. Qualitative evaluation included assessment of cortical maturation, corticomedullary differentiation, nephron development and sequential stages of glomerular maturation. Quantitative morphometric analysis was performed using a calibrated ocular micrometer to measure cortical thickness at standardised sites in each specimen. All observations and measurements were documented for individual specimens and subsequently grouped according to eight gestational age categories (14-28 weeks) to evaluate the chronological progression of renal histogenesis. Results: The Nephrogenic Zone (NZ) thinned progressively from 14 to 28 weeks. Concurrently, mean cortical thickness increased significantly from 754.68±53.40 μm to 2078.62±58.92 μm {Analysis of Variance (ANOVA), p<0.001}. This demonstrated a highly significant linear growth pattern (R2=0.992), with the highest rate of growth occurring at 22-24 weeks (an increase of 284.63 μm). Glomerular maturation followed a centrifugal pattern, with primitive structures dominating superficially at 14-16 weeks. Proximal Convoluted Tubules (PCT) and Distal Convoluted Tubules (DCT) emerged at 18 weeks, becoming well-defined by 22 weeks. Corticomedullary differentiation began at 16-18 weeks; complete demarcation, well-organised pyramids and mature Ducts of Bellini were distinguishable by 28 weeks. Conclusion: The present study establishes a precise morphological timeline for mid-gestational renal histogenesis. The 22-28 week window represents a phase of intense maturation characterised by significant cortical growth and marked nephron polymorphism. These findings serve as a normative anatomical baseline essential for the prenatal diagnosis of congenital anomalies and understanding the impact of preterm birth on nephron endowment. | |||||||
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| Keywords : Congenital anomalies, Crown-rump length, Glomerulogenesis, Nephrogenic zone | |||||||
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DOI and Others :
DOI: 10.7860/IJARS/2026/90905.3122
Date of Submission: Jun 02, 2026 Date of Peer Review: Jun 26, 2026 Date of Acceptance: Jul 19, 2026 Date of Publishing: Sep 01, 2026 AUTHOR DECLARATION: • Financial or Other Competing Interests: None • Was Ethics Committee Approval obtained for this study? Yes • Was informed consent obtained from the subjects involved in the study? Yes • For any images presented appropriate consent has been obtained from the subjects. Yes PLAGIARISM CHECKING METHODS: • Plagiarism X-checker: Jun 09, 2026 • Manual Googling: Jul 13, 2026 • iThenticate Software: Jul 18, 2026 (1%) ETYMOLOGY: Author Origin EMENDATIONS: 8 |
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