Renal lymphangiomatosis, a rare differential diagnosis for autosomal recessive polycystic kidney disease in pediatric patients

Radiology Case Reports

Amin Al Zahrani, MD¹  Mohammed O. Al Otibi, MD¹  Amna A. Kashgari, MD²  Nabil Ozair, MD²  Khalid Al Fakeeh, MD³ 

[1] Department of Medical Imaging, Intervention Radiology Section, King Abdullah Specialized Children's Hospital, King Abdulaziz Medical City, Ministry of National Guard, PO Box 22490, Riyadh, KSA;Department of Medical Imaging, King Abdullah Specialized Children's Hospital, King Abdulaziz Medical City, Ministry of National Guard, PO Box 22490, Riyadh, KSA;Department of Pediatric, King Abdullah Specialized Children's Hospital, King Abdulaziz Medical City, Ministry of National Guard, PO Box 22490, Riyadh, KSA;

关键词: Ultrasound;    Magnetic resonance imaging;    Lymphangiomatosis;    Kidney;   

DOI  :  10.1016/j.radcr.2016.11.016

来源: DOAJ

【 摘 要 】

Renal lymphangiomatosis is a rare, benign malformation, characterized by developmental malformation of the perirenal, peripelvic, and intrarenal lymphatics. Radiologist knowledge of the unique radiological features of this entity helps patient's safety in terms of management. We study the case of a 27-month-old boy presented to the emergency department with upper respiratory tract infection. He had a high blood pressure and had been diagnosed earlier with autosomal recessive polycystic kidney disease based on renal ultrasound findings. Because the clinical presentation and laboratory work of the patient did not support the diagnosis of autosomal recessive polycystic kidney disease, further, extensive work-up was performed, which confirmed the diagnosis of renal lymphangiomatosis. This case report emphasizes the imaging features of this rare entity to promote early diagnosis and better patient care.

【 授权许可】

Unknown