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Introduction: Adrenal myelolipomas are uncommon benign adrenal tumors, which mostly occur unilaterally. We describe a rare case of giant bilateral adrenal myelolipoma mistaken for retroperitoneal liposarcoma.
Case Presentation: A 49-year-old man developed fever, left flank pain, and a large mass in his left abdomen.
Multiorgan and Multisystem Involvement During Primary HIV Infection: A Case Report With a Literature Review.
Cureus
November 2024
Urology, All India Institute of Medical Sciences, Rishikesh, Rishikesh, IND.
The initial six months following HIV infection have a high viral load. Nonspecific presentations might lead to the missing primary HIV diagnosis. Multiorgan and multisystem diagnosis is a rare presentation of primary HIV.
View Article and Find Full Text PDFDepressive Symptoms in Adults with Autosomal Dominant Polycystic Kidney Disease.
Kidney360
December 2024
Department of Medicine, Division of Nephrology, University of Maryland School of Medicine, Baltimore, Maryland.
Background: Individuals with autosomal dominant polycystic kidney disease (ADPKD) face mental health challenges linked to disease progression and its heritable nature. Prior studies reported mixed associations between depressive symptoms and ADPKD severity and progression. Here, we assessed depressive symptoms and disease severity over three years in ADPKD patients without end-stage kidney disease.
View Article and Find Full Text PDFIliopsoas Abscess Mimicking a Lower Motor Neuron Lesion: A Diagnostic Challenge.
Cureus
November 2024
Internal Medicine, Mid and South Essex NHS Foundation Trust, Southend-on-Sea, GBR.
Iliopsoas abscess is a rare infection that presents with a triad of fever, back pain, and hip pain. However, due to the anatomical proximity of the psoas muscle to various structures, an abscess in this region can manifest with nonspecific symptoms, leading to potential misdiagnosis and delayed diagnosis, which can be fatal. We report a case of a 54-year-old female who presented to the emergency department with right-sided flank pain and symptoms resembling lower motor neuron disorder.
View Article and Find Full Text PDFEosinophilic solid and cystic renal cell carcinoma: A case study with pathological correlates.
Int J Surg Case Rep
December 2024
Damascus Hospital, Damascus, Syria.
Introduction And Significance: Eosinophilic solid and cystic renal cell carcinoma (ESC RCC) is a rare renal tumor primarily associated with female patients and those with tuberous sclerosis complex (TSC). Despite lacking distinct clinical or radiological features, its unique histological characteristics allow for differentiation from other renal neoplasms. While it often exhibits indolent growth, metastatic potential remains a concern.
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