Fraley syndrome

From WikiMD.org
Jump to navigation Jump to search

Fraley syndrome is a rare medical condition characterized by the compression of the renal calyx by a segment of the renal artery. This condition was first described by the American urologist John C. Fraley in 1968.

Pronunciation

The term "Fraley syndrome" is pronounced as "Fray-lee sin-drome".

Etymology

The syndrome is named after John C. Fraley, an American urologist who first described the condition in 1968.

Symptoms

The primary symptom of Fraley syndrome is hematuria (blood in the urine), which is often painless. Other symptoms may include flank pain, kidney stones, and recurrent urinary tract infections.

Diagnosis

Diagnosis of Fraley syndrome is typically made through imaging studies such as ultrasound, computed tomography (CT) scan, or magnetic resonance imaging (MRI). These tests can reveal the characteristic finding of a dilated upper renal calyx compressed by a segment of the renal artery.

Treatment

Treatment for Fraley syndrome typically involves surgical intervention to relieve the compression of the renal calyx. This may include nephrectomy (removal of the kidney), pyeloplasty (reconstruction of the renal pelvis), or renal artery revascularization.

Related Terms

External links

Esculaap.svg

This WikiMD dictionary article is a stub. You can help make it a full article.


Languages: - East Asian 中文, 日本, 한국어, South Asian हिन्दी, Urdu, বাংলা, తెలుగు, தமிழ், ಕನ್ನಡ,
Southeast Asian Indonesian, Vietnamese, Thai, မြန်မာဘာသာ, European español, Deutsch, français, русский, português do Brasil, Italian, polski