Carlos Alfredo Bedia Castillo

Dr. Carlos Alfredo Bedia Castillo

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Research Focus & Metrics

Academic Career Length

3Years (2024-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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16 December 2024 in Medical Sciences
Verified
Journal Article
Open access
PDF file
MDMarco Antonio Moises Dominguez Davalos
Marco Antonio Moises Dominguez Davalos
JFJosé Carlos De La Flor
José Carlos De La Flor
CCCarlos Alfredo Bedia Castillo
Carlos Alfredo Bedia Castillo
RCRoxana Lipa Chancolla
Roxana Lipa Chancolla
CTCelia Rodríguez Tudero
Celia Rodríguez Tudero
MCMichael Cieza
Michael Cieza
Background: Lupus podocytopathy (LP) is a non-immune complex-mediated glomerular lesion in systemic lupus erythematosus (SLE), characterized by the diffuse effacement of podocyte processes without immune complex deposition or with only mesangial immune complex deposition. LP is a rare cause of nephrotic syndrome in SLE patients with implications for prognosis and treatment. Case Report: We present the case of a 28-year-old woman with a medical history of type 1 diabetes mellitus (T1DM) who presented with lower limb edema, dyspnea, hypercholesterolemia, with nephrotic range proteinuria, without acute kidney injury, and laboratory findings compatible with auto-immune hemolytic anemia. They had negative infectious serology, positive antinuclear antibody (ANA), and an eye fundus examination showing diabetic retinopathy. A biopsy was performed to define the etiology of the renal involvement, which was compatible with LP. Following immuno-suppressive and antiproteinuric therapy, the patient evolved with the complete remission of the nephrotic syndrome. Conclusions: Lupus podocytopathy is an infrequent anatomopathological entity, so this case is presented as the first reported in Peru, and a literature review is made.

21 July 2025 in Diseases
Verified
Journal Article
Open access
PDF file
MDMarco Antonio Moises Dominguez Davalos
Marco Antonio Moises Dominguez Davalos
RCRaúl Valenzuela Córdova
Raúl Valenzuela Córdova
CTCelia Rodríguez Tudero
Celia Rodríguez Tudero
EMElena Jiménez Mayor
Elena Jiménez Mayor
CCCarlos Alfredo Bedia Castillo
Carlos Alfredo Bedia Castillo
JNJavier A. Neyra
Javier A. Neyra
Background/Objectives: Acetazolamide is widely used for acute mountain sickness (AMS) prophylaxis. Whilst generally safe, acute kidney injury (AKI) is a rare but serious adverse event. We present a case of anuric AKI following minimal exposure to acetazolamide, contributing to the limited literature on its nephrotoxicity at prophylactic doses. Methods: A 54-year-old previously healthy male ingested 250 mg/day of oral acetazolamide for two days. He developed acute anuria and lumbar pain. Diagnostic evaluation included laboratory tests, imaging, microbiological cultures, autoimmune panels, and diuretic response. No signs of infection, urinary tract obstruction, or systemic disease were found. Results: The patient met KDIGO 2012 criteria for stage 3 AKI, with peak serum creatinine of 10.6 mg/dL and metabolic acidosis. Imaging confirmed non-obstructive nephrolithiasis. Conservative treatment failed; intermittent hemodialysis was initiated. Renal function recovered rapidly, with the normalization of serum creatinine and urinary output by day 4. Conclusions: This case represents the lowest cumulative dose of acetazolamide reported to cause stage 3 AKI. The findings support a pathophysiological mechanism involving sulfonamide-induced crystalluria and intratubular obstruction. Physicians should consider acetazolamide in the differential diagnosis of AKI, even with short-term prophylactic use.