Results 181 to 190 of about 65,128 (262)

Hematuria, Proteinuria, and Acute Kidney Injury in a Patient Presenting with Abdominal Pain. [PDF]

Kidney360
Alexandre I, Theias R, Carrilho P.
europepmc   +1 more source

Cervical Skip Metastases and Extensive Central Venous Thrombosis as the Initial Presentation of High‐Grade Prostate Adenocarcinoma With Discordant PI‐RADS 3 Findings: A Case Report and Diagnostic Challenge

Clinical Case Reports, Volume 14, Issue 6, June 2026.
ABSTRACT Prostate cancer can initially present with cervical lymph node “skip” metastases and extensive central venous thrombosis, without pelvic or bone involvement. A PI‐RADS 3 lesion on mpMRI does not exclude high‐grade (Gleason 5 + 5 = 10) disease. Unexplained thrombosis in elderly men warrants prostate cancer investigation.
Yuchun Luo, Benhui Lai, Juncheng Huang
wiley   +1 more source

AKI After Hepatic Histotripsy. [PDF]

Kidney Int Rep
Bhutta S, Wanchoo R, Sakhiya V, Gholami S, Devoe C, Jhaveri KD.   +5 more
europepmc   +1 more source

Late‐Onset Diagnosis of Tuberous Sclerosis Complex Revealed by Renal Angiomyolipoma: A Case Report

Clinical Case Reports, Volume 14, Issue 6, June 2026.
ABSTRACT Tuberous sclerosis complex (TSC) is a rare autosomal dominant disorder characterized by multisystem hamartomas caused by pathogenic variants in TSC1 or TSC2. It is typically diagnosed in childhood, most often because of neurological or dermatological manifestations.
A. Fekih, W. Heni, C. Messaoudi, Y. Selmi, D. Touati, Z. Elloumi, J. Labidi   +6 more
wiley   +1 more source

Case Report: Diagnosis and management of primary malignant melanoma of the bladder: a case-based review. [PDF]

Front Oncol
Hou X, Xu X, Chen Y, Jiang B, Xu Y, Zhang H.   +5 more
europepmc   +1 more source

Catastrophic Antiphospholipid Syndrome in a Young Female Complicated by Systemic Lupus Erythematosus and Left Atrial Myxoma: A Rare Case Report

Clinical Case Reports, Volume 14, Issue 6, June 2026.
ABSTRACT Catastrophic antiphospholipid syndrome (CAPS) is a fulminant and rare variant of antiphospholipid syndrome characterized by rapidly progressive multiorgan thrombosis and a high mortality rate. Its diagnosis is often challenging due to overlapping clinical features with sepsis, thromboembolic disorders, and systemic autoimmune diseases.
Nazmin Ahmed, Mohammad Nazrul Hossain, Abdullah Salman, Sabrina Yesmin, S. M. G. Saklayen   +4 more
wiley   +1 more source

Rapidly Progressive IgA Nephropathy in a Patient With a History of Breast Cancer: A Case Report and Literature Review. [PDF]

Case Rep Nephrol
Montesinos RL, Marca EQ, Torrico CA, Herbas DS, Limachi LC, Arenas ZT, Mamani WV.   +6 more
europepmc   +1 more source

A Rare Presentation of Granulomatosis With Polyangiitis: A Case Report and Literature Review

Clinical Case Reports, Volume 14, Issue 6, June 2026.
ABSTRACT Granulomatosis with polyangiitis (GPA) is a rare ANCA‐associated necrotizing vasculitis that predominantly affects the respiratory tract and kidneys. Gastrointestinal involvement is uncommon, and pancreatic manifestations are exceedingly rare. Diffuse alveolar hemorrhage (DAH) represents a severe and potentially fatal complication. We report a
Anil Shahi, Ayush Neupane, Bishaka Adhikari   +2 more
wiley   +1 more source

Massive hemorrhage and cardiac arrest due to ureteroarterial fistula following nephroureteral stent removal: A case report. [PDF]

Urol Case Rep
Campbell JA, Lee S, Su ZT, Wilkins L, Gabrielson AT, Galansky LB, Alshak MN, Higgins MI, Garman TS, Patel SH, Burnett AL, Cohen AJ.   +11 more
europepmc   +1 more source