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RIRS Triumphs in medullary sponge kidney with incomplete ureteral duplication: Report of a rare case.
Asian J Surg
November 2024
Department of Urology, Key Laboratory of Disease of Urological Systems, Gansu Nepho-Urological Clinical Center, The Second Hospital of Lanzhou University, 80 Cui YinMen Street, Chen-guan District, Lanzhou, Gansu, 730030, China. Electronic address:
Phenotypic Discordance among Siblings with Autosomal Recessive Polycystic Kidney Disease: Case Report and Review of the Literature.
Nephron
December 2024
Division of Medical Genetics, McGill University Health Centre, Montreal, Québec, Canada.
Article Synopsis
- The study focuses on missense variants in the PKHD1 gene, which are linked to varying severity of autosomal recessive polycystic kidney disease (ARPKD), highlighting how different genetic expressions can lead to diverse health outcomes in individuals.
- It presents a case of two adult siblings who share biallelic missense variants but exhibit significantly different health experiences: one suffers from severe kidney complications and requires transplants, while the other maintains nearly normal kidney function into middle age.
- The findings emphasize that specific genetic compositions, particularly those involving hypomorphic variants, may contribute to the inconsistent presentation of symptoms, or "phenotypic discordance," even among siblings.
Nursing care during management of recurrent pheochromocytoma: A case study.
Nurs Crit Care
October 2024
School of Nursing, Putian University, Putian, China.
Article Synopsis
- Pheochromocytoma, especially in patients with multiple endocrine neoplasia type 2, poses a challenge due to the risk of recurrence after surgery, necessitating effective management strategies.
- A case study involved a 34-year-old woman who, after a history of surgery for pheochromocytoma, faced recurrent episodes leading to severe complications, including cardiac arrest, but ultimately recovered through innovative treatment approaches.
- The study emphasizes the importance of a comprehensive nursing management plan that includes close monitoring, patient positioning, and psychological support to enhance recovery outcomes for similar patients.
Rare type of Bellini Duct Carcinoma in a Patient With Cacchi-Ricci Disease: A Case Report and Mini-Review.
Clin Genitourin Cancer
December 2024
Department of Urology, Ghent University Hospital, ERN eUROGEN accredited center, Ghent, Belgium. Electronic address:
Article Synopsis
- *Diagnosing MSK can be challenging, especially when there is a concurrent renal mass, which might complicate the imaging results.
- *The report presents a rare case of Bellini duct carcinoma occurring in a patient with MSK, along with a review of related literature on this complex kidney disorder.
Corrigendum to "Atypical Clinical Presentation of Autosomal Recessive Polycystic Kidney Mimicking Medullary Sponge Kidney Disease" [ Volume 7, Issue 4, April 2022, Pages 916-919].
Kidney Int Rep
August 2024
Institut National de la Santé et de la Recherche Médicale, UMR S 1155, Paris, France.
Article Synopsis
- This text indicates that there is a correction to an article identified by the DOI number 10.1016/j.ekir.2021.11.035.
- The correction aims to address inaccuracies or errors that were found in the original publication.
- Such corrections are important for maintaining the accuracy and integrity of academic literature.
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