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Updated: Sep 8, 2025

Image Acquisition Method for the Sonographic Assessment of the Inferior Vena Cava
Published on: January 13, 2023
Anatomical features of coexisting horseshoe kidney and double inferior vena cava
Naofumi Horio1, Narumi Miyaura1, Kenta Nagahori2
1Tokai University School of Medicine, Isehara, Kanagawa, Japan.
Insights
This study details a rare anatomical finding of horseshoe kidney (HSK) and double inferior vena cava (DIVC) in a cadaver. Recognizing this complex renal and vascular variation is crucial for surgical and radiological procedures.
Area of Science:
- Anatomy
- Embryology
- Surgical Pathology
Background:
- Horseshoe kidney (HSK) and double inferior vena cava (DIVC) are rare congenital anomalies.
- Coexistence of HSK and DIVC presents unique anatomical challenges.
- Embryological development of kidneys and IVC occurs concurrently.
Purpose of the Study:
- To document a rare case of coexisting horseshoe kidney and double inferior vena cava.
- To analyze the embryological and clinical implications of this combined anatomical variation.
- To emphasize the importance of recognizing such variations in clinical practice.
Main Methods:
- Cadaveric dissection of a 96-year-old Japanese male.
- Detailed anatomical examination of renal and vascular structures.
- Histological analysis of the renal isthmus.
Main Results:
- Fusion of kidneys by an isthmus below the inferior mesenteric artery (HSK).
- Presence of a double inferior vena cava (DIVC) with no communicating veins.
- Multiple renal arteries and an aberrant renal vein noted.
- Histology showed atrophic tubules and increased connective tissue in the isthmus.
Conclusions:
- Coexisting HSK and DIVC demonstrate significant anatomical variability.
- Awareness of this rare variation is vital for surgeons and radiologists.
- Early embryological abnormalities can lead to complex retroperitoneal variations.
Abstract:
To describe a rare case of coexisting horseshoe kidney (HSK) and double inferior vena cava (DIVC) observed during a cadaveric dissection course and to analyze the embryological and clinical implications of this anatomical variation. A detailed anatomical dissection of a 96-year-old Japanese male cadaver was performed during a gross anatomy course. The kidneys were fused by a fibrous and parenchymal isthmus below the inferior mesenteric artery. Four right renal arteries and three left renal arteries were identified, along with an additional renal vein arising from the isthmus and coursing to the left adrenal gland. The right and the left IVCs ascended bilaterally along the aorta, with no communicating veins observed. Histological findings revealed atrophic renal tubules in the isthmus, with increased connective tissue. This report highlights the high variability of renal and vascular anatomy in coexisting HSK and DIVC. Recognition of such variations is essential for radiologists and surgeons to avoid complications during renal transplantation, vascular surgery, and imaging interpretation. In addition, the kidneys and the IVC development occur simultaneously between weeks 4 and 8 of embryogenesis. Therefore, abnormalities of retroperitoneal structures that occur during embryological development can lead to variations.
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