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ArticleClinical medicine insights. Case reports2026

Incidental Multisystem Anomalies in an Adolescent Female: A Case Report of a Diagnostic Dilemma.

Deekshitha Alla, Pranathi Chanti, Moksh Sanjay Khetan, Srinidhi Appala, Rohit Rao Dugyala, Sagnik Roy, Keerthana Chittepu, Pritha Mohanta, Ram Prasanjith Reddy Bollampalli, Ruth Getaneh Bayeh

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Article in Clinical medicine insights. Case reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

10 authors.

Deekshitha AllaDepartment of General Medicine, Andhra Medical College, India.
Pranathi ChantiDepartment of Gastroenterology and Hepatology, Mayo Clinic, USA.
Moksh Sanjay KhetanCardiovascular Imaging Research Center, Indiana University School of Medicine, USA.
Srinidhi AppalaDepartment of General Medicine, All India Institute of Medical Sciences Bhopal, India.
Rohit Rao DugyalaDepartment of General Medicine, Gandhi Medical College and Hospital, India.
Sagnik RoyDepartment of General Medicine, KPC Medical College and Hospital, India.
Keerthana ChittepuDepartment of General Medicine, RKDF Medical College Hospital & Research Centre, India.
Pritha MohantaDepartment of General Medicine, Hi-Tech Medical College & Hospital, India.
Ram Prasanjith Reddy BollampalliDepartment of General Medicine, MediCiti Institute of Medical Sciences, India.
Ruth Getaneh BayehDepartment of General Medicine, Adama General Hospital and Medical College, Ethiopia.ORCID https://orcid.org/0009-0000-0069-3781

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Congenital anomalies of the urogenital system frequently coexist with renal abnormalities due to their shared origin from the intermediate mesoderm. Skeletal anomalies may also be associated, reflecting overlapping embryological development of mesodermal derivatives. Such multisystem involvement can pose a diagnostic challenge, particularly when identified incidentally. Case Presentation: We report a 15-year-old female who presented with abdominal swelling and pain, later diagnosed as an umbilical hernia. During radiological evaluation, incidental findings of right renal agenesis, scoliosis, and a bicornuate uterus were identified. The patient underwent successful surgical management of the umbilical hernia. This case highlights the importance of recognizing coexisting anomalies and adopting an integrated approach in evaluation and management. Conclusion: This case highlights the need for a systematic, bidirectional evaluation when a congenital anomaly is identified, particularly involving the renal, genital, and skeletal systems. A syndromic perspective is essential to avoid missed diagnoses, facilitate appropriate follow-up, and anticipate long-term implications in such patients.

Indexed as

bicornuate uterusmüllerian duct anomalymultisystem congenital anomalyrenal agenesisscoliosis

Identifiers

PMID42428543
PMCPMC13346742

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