Archive : Article / Volume 2, Issue 1

Case Report | DOI: https://doi.org/10.58489/2836-5127/003

Bilateral ectopic pelvic kidneys: The novel association with liver hemangioma

Aamir Jalal Al-Mosawi,

Advisor doctor and expert trainer, Baghdad Medical City and the National Training and Development Center, Iraqi Ministry of Health, Baghdad, Iraq

Correspondng Author: Aamir Jalal Al-Mosawi

Citation: Aamir Jalal Al-Mosawi, (2023). Bilateral ectopic pelvic kidneys: The novel association with liver hemangioma. Journal of Radiology Research and Diagnostic Imaging. 2(1). DOI: 10.58489/2836-5127/003

Copyright: © 2023, Aamir Jalal Al-Mosawi, this is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Received Date: 2022-12-10, Received Date: 2022-12-10, Published Date: 2023-01-09

Abstract Keywords: Bilateral ectopic pelvic kidneys, hepatic hemangioma.

Abstract

Background: Renal ectopia is a congenital abnormality in which one or both kidneys are located in an unusual position because of failure of normal ascend from its origin in the true pelvis. Several types of renal ectopia with or without fusion or other associated renal and abdominal visceral abnormalities have been reported. We have previously reported the case forty-one of crossed unfused renal ectopia, and the aim of this paper is to report the association of bilateral ectopic pelvic kidneys with liver hemangioma.                        

Patients and methods: The case of a woman in her mid-forties with renal and hepatic abnormalities on pelvic and abdominal ultrasound was studied.

Results: A woman in her mid-forties was having recurrent lower abdominal pain or discomfort and recurrent urinary tract infection. Ultrasound showed that both kidneys were ectopic and were located in the pelvic cavity. Both kidneys were normal in size, texture, parenchymal thickness, and had normal cortico-modularly differentiation. There was mild splitting of the pelvi-calyceal system suggesting infection. Both ureters were normal. The liver was normal in size with homogenous texture, but there was a right lobe well-defined echogenic soft tissue mass, hemangioma. Renal function tests showed normal findings.

Conclusion: Bilateral ectopic pelvic kidneys is a rare congenital condition that has not been reported to occur in association with hepatic hemangioma. This paper reports the novel association of bilateral ectopic pelvic kidneys with hepatic hemangioma.

Introduction

Renal ectopia is congenital abnormality in which one or both kidneys are located in an unusual position because of failure of normal ascend from its origin in the true pelvis. Several types of renal ectopia with or without with or without fusion or other associated renal and abdominal visceral abnormalities have been reported since the early report of Polk in I882 [1, 2, 3]. We have previously reported the case forty-one of crossed unfused renal ectopia [1], and the aim of this paper is to report the association of bilateral ectopic pelvic kidneys with liver hemangioma.

Patients and methods

The case of a woman in her mid-forties with renal and hepatic abnormalities on pelvic and abdominal ultrasound was studied.

Results

A woman in her mid-forties was found to have renal and hepatic abnormalities on pelvic and abdominal ultrasound during the evaluation after treatment for urinary tract infection. She was having recurrent lower abdominal pain or discomfort and recurrent urinary tract infection.  Ultrasound (Figure-1) showed that both kidneys were ectopic, and were located in the pelvic cavity. Both kidneys were normal in size, texture, parenchymal thickness, and had normal cortico-modularly differentiation. There was mild splitting of the pelvi-calyceal system suggesting infection. Both ureters were normal. The liver was normal in size with homogenous texture with a right lobe well-defined echogenic soft tissue mass, hemangioma. She had normal blood pressure and renal function tests showed normal findings.

Discussion

As early as 1931 Howard L Tolson emphasized that ectopic kidneys can be structurally and functionally normal and remain asymptomatic or associated with mild dull pain and urinary tract infections [4].

Boujnah et al (1989) from Tunisia emphasized that bilateral pelvic ectopic kidneys is a rare congenital condition, and they reported 50 cases of pelvic ectopic kidneys observed during 12 years. 47 patients had unilateral pelvic ectopic kidney, two patients had bilateral pelvic ectopic kidneys, and one patient had pelvic ectopic kidney solitary pelvic ectopic kidney. Eighteen patients had healthy ectopic kidneys. Thirty-two patients had diseased ectopic kidney including twenty-one patients with renal stones and seven patients with uretero-pelvic junction disease. 

Boujnah et al from Tunisia emphasized the diagnostic value of renal ultrasound which can help in avoiding other useless and expensive investigations [5].

Figure-1: Ultrasound showed that the both kidneys were ectopic and were located in the pelvic cavity

Hirano and colleagues (1992) reported the incidental detection of bilateral ectopic pelvic kidneys by radioisotope angiography [6]. 

Alonso Domínguez (1996) also emphasized the rarity of bilateral pelvic ectopic kidneys and reported a case with an unusual presentation [7].

Gokalp and colleagues (2010) reported a case with bilateral ectopic kidneys associated with vascular anomaly and hypertension and renal dysfunction [8].

Hemangiomas including liver hemangiomas are benign vascular tumors that are generally observed during infancy. Liver hemangioma is the most common benign tumor of the liver [8, 9]. Brodsky et al (1987) reported that during the performance of high-resolution real-time abdominal sonography, hemangioma small echogenic hepatic masses are frequently discovered [10].

Lipman and Tumeh (1990) from Boston, Massachusetts emphasized that the diagnosis of small liver hemangiomas, less than 3 cm can be made with abdominal ultrasound study [11].

Al-Durazi et al (2003) from Bahrain reported the incidental finding of a case of hepatic hemangioma while performing a routine renal and pelvic ultrasound in patients with urinary retention associated with benign prostatic hyperplasia [12].

Mungovan and colleagues (1994) emphasized that the size of the majority of hepatic hemangiomas don’t increase in size for months and years, and an increase in size demands further evaluation [13].

Conclusion

Bilateral ectopic pelvic kidneys are a rare congenital condition that has not been reported to occur in association with hepatic hemangioma. This paper reports the novel association of bilateral ectopic pelvic kidneys with hepatic hemangioma.

References

  1. Al-Mosawi AJ. The case forty-one of crossed unfused renal ectopia. International Journal of Recent Innovations in Medicine and Clinical Research (ISSN: 2582-1075) May 10, 2020; 2(1):17-21.
  2. Cullen TS. A right pelvic kidney; Absence of the left; Absence of the uterus; Both ovaries in the inguinal canal. Surg Gyn and Obst 1910; 11 (1):73.
  3. Looney WW, Dodd DL. An ectopic (pelvic) completely fused (cake) kidney associated with various anomalies of the abdominal viscera. Ann Surg 1926 Oct; 84(4):522-4.
  4. Tolson HL. Ectopic (Pelvic) Kidney. Ann Surg 1931 Apr; 93(4):880-5. Doi: 10.1097/0 0000658-193104000-00011.
  5. Boujnah H, Abid I, Moalla N, Zmerli S. Le rein pelvien. A propos de cinquante cas [Pelvic kidney. Apropos of 50 cases]. Ann Urol (Paris). 1989; 23(1):11-6 [Article in French].
  6. Hirano T, Igarashi H, Mogi Y. Bilateral ectopic pelvic kidneys incidentally demonstrated by radioisotope angiography. Clin Nucl Med. 1992 Oct; 17(10): 831.Doi: 10.1097/000 03072-199210000-00022.
  7. Alonso Domínguez FJ. Riñón ectópico pelviano bilateral [Bilateral pelvic ectopic kidney]. Arch Esp Urol 1996 Nov; 49(9):977-8. [Article in Spanish].
  8. Gokalp G, Hakyemez B, Erdogan C. Vascular anomaly in bilateral ectopic kidney: a case report. Cases J 2010 Jan 5; 3:5. Doi: 10.1186/1757-1626-3-5.
  9. Al-Mosawi AJ. Esquirol-Séguin-Down syndrome associated with hepatic hemangioma: An Association not previously reported in the literature. Case Reports & Research Practices in MEDICINE (ISSN: 2771-4845) March 5, 2022; 2 (1): 34-36. Doi: 10.5281/zenodo.6334870.
  10. Al-Mosawi AJ. Uncomplicated cutaneous infantile strawberry hemangioma: Educational images and evidence-based recommendation. Case Reports & Research Practices in MEDICINE (ISSN: 2771-4845) March 5, 2022; 2 (1): 31-33. Doi: 10.5281/ zenodo.6334853.
  11. Brodsky RI, Friedman AC, Maurer AH, Radecki PD, Caroline DF. Hepatic cavernous hemangioma: diagnosis with 99mTc-labeled red cells and single-photon emission CT. AJR Am J Roentgenol 1987 Jan; 148(1):125-9. Doi: 10.2214/ajr.148.1.125.
  12. Lipman JC, Tumeh SS. The radiology of cavernous hemangioma of the liver. Crit Rev Diagn Imaging. 1990; 30(1):1-18.
  13. Al-Durazi MH, Al-Helo HA, Al-Reefi SM, Al-Sanaa SM, Abdulwahab WA. Routine ultrasound in acute retention of urine. Saudi Med J 2003 Apr; 24(4):373-5.
  14. Mungovan JA, Cronan JJ, Vacarro J. Hepatic cavernous hemangiomas: lack of enlargement over time. Radiology 1994 Apr; 191(1):111-3. Doi: 10.1148/ radiology.191. 1.8134554.

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