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We report a 10-year-old boy with pelvic lipomatosis causing chronic urinary retention. CT scan features, therapy and review of the literature are discussed.

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Inferior vena cava agenesis (IVCA) is a rare congenital anomaly that can be asymptomatic or present with vague, nonspecific symptoms, such as abdominal or lower back pain, or deep vein thrombosis (DVT). Here, we present a 55-year-old male who came with painless swelling and redness of his left lower limb. On examination, swelling and redness were noted extending from the left foot to the upper thigh; it was also warm compared to his right lower limb. Venous Doppler ultrasound was done which showed DVT extending up to the common femoral vein. Subsequently, computed-tomography (CT) of the chest and abdomen was done to exclude malignancy or venous flow obstruction; it revealed congenital absence (agenesis) of the infrarenal inferior vena cava (IVC).

Primary amyloidosis of the genitourinary tract is a rare clinical entity with an excellent prognosis in most cases. It is of interest to the urologist as it mimics malignancy. The definitive diagnosis is made on histologic examination and by excluding secondary causes of amyloidosis. We present 4 patients with primary localized amyloidosis of the genitourinary tract who were treated with transurethral resections alone with satisfactory outcome.