A case of adrenal myelolipoma complicated with Prader‐Willi syndrome

Author:

Inoue Toru12,Todaka Masahiro2,Nakazono Yuichi3,Fukata Yoko4,Shin Toshitaka1

Affiliation:

1. Department of Urology, Faculty of Medicine Oita University Yufu‐City Oita Japan

2. Department of Urology, Beppu Medical Center National Hospital Organization Beppu Oita Japan

3. Department of Pathology Beppu Medical Center, National Hospital Organization Beppu Oita Japan

4. Department of Diabetes and Endocrinology Beppu Medical Center, National Hospital Organization Beppu Oita Japan

Abstract

IntroductionPrader‐Willi syndrome is a congenital disorder that occurs in one in 10 000–30 000 children and is characterized by obesity, short stature, and intellectual disability.Case presentationA 24‐year‐old male patient with Prader‐Willi syndrome presented with an enlarged adrenal tumor. Computed tomography detected a well‐defined mass. Magnetic resonance imaging revealed an increased signal intensity predominantly in fatty areas, suggesting adrenal myelolipoma. Laparoscopic left adrenalectomy was performed. Postoperatively, the patient developed mild pulmonary atelectasis, myelolipoma was confirmed by histopathology, and there was no recurrence at approximately 2 years postoperatively.ConclusionThis is the first report of Prader‐Willi syndrome complicated with adrenal myelolipoma, which was removed laparoscopically.

Publisher

Wiley

Subject

Urology

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