Evidence map›Paper›PMID 41080267›Full record

ArticleCureus2025

Ectopic Kidney Masquerading as a Pelvic Mass: A Case Report.

Lakshmi Kandhan L, Venkata Ramana K, Velmurugan Palaniyandi, Hariharasudhan Sekar, Sriram Krishnamoorthy

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In one paragraph

Article in Cureus, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

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3citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

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4 · The record

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PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Lakshmi Kandhan LUrology, Sri Ramachandra Institute of Higher Education and Research, Chennai, IND.
Venkata Ramana KUrology, Sri Ramachandra Institute of Higher Education and Research, Chennai, IND.
Velmurugan PalaniyandiUrology, Sri Ramachandra Institute of Higher Education and Research, Chennai, IND.
Hariharasudhan SekarUrology, Sri Ramachandra Institute of Higher Education and Research, Chennai, IND.
Sriram KrishnamoorthyUrology, Sri Ramachandra Institute of Higher Education and Research, Chennai, IND.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Renal ectopia is a congenital anomaly caused by abnormal migration of the kidneys during the process of embryogenesis. Under typical development, the kidneys ascend to the lumbar region during the early gestational period. A failure in this process can result in ectopic kidneys, most commonly found in the pelvis. Although often asymptomatic, pelvic kidneys can be complicated by pelviureteric junction obstruction (PUJO), infection, reflux, or malrotation in a few cases. We present a rare case of a pelvic kidney with PUJO presenting as a lower abdominal mass in an elderly female. A 60-year-old female presented to our urology clinic with progressive lower abdominal fullness and vague discomfort for several months. Clinical examination revealed a firm, non-tender mass measuring 15 × 8 cm in the hypogastric and iliac regions. Blood investigations and renal function tests were within normal limits. Contrast-enhanced CT urography revealed a grossly hydronephrotic left pelvic kidney with parenchymal thinning and no contrast excretion. No calculi or masses were identified. A diethylenetriamine pentaacetic acid (DTPA) renogram confirmed severely impaired function of the ectopic kidney. The patient underwent cystoscopy with ureteric catheterization, followed by left nephrectomy. Histopathological examination confirmed chronic pyelonephritis in the hydronephrotic kidney. A pelvic kidney is an uncommon congenital anomaly identified in a small proportion of births. PUJO is one of the most common causes of hydronephrosis in ectopic kidneys. Detailed imaging and functional studies are essential for diagnosis and management. Delayed presentation in adults highlights the need to consider renal ectopia in differential diagnosis. This case emphasizes the importance of recognizing ectopic kidneys in adults presenting with abdominal masses. Timely imaging and functional assessment aid in appropriate surgical decision-making, especially in non-functioning kidneys where nephrectomy prevents long-term complications.

Indexed as

ectopic kidneyhydronephrosisnephrectomypelvic kidneypelviureteric junction obstructionrenal anomalies

Identifiers

PMID41080267
PMCPMC12514948

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