Abstract

IntroductionIsolated lymphedema of the penis is extremely rare: combined involvement of the scrotum and penis is the norm. Furunculosis as a cause is not, to our knowledge, previously reported. We present a case of isolated penile lymphedema that responded to excision of lymphedematous tissue and reconstruction with flaps.Case presentationA 32-year-old Arab man presented with a three-year history of a gradually increasing, painless penile swelling. Our patient's main complaint was non-erectile sexual dysfunction. The swelling was preceded by at least three prior episodes of severe furunculosis at the penile root. He had no other contributory past medical or family history. On examination there was gross penile enlargement, maximally at the mid shaft, associated with thickened skin at the sites of prior furunculosis. The glans and scrotum were normal. Both testes were palpable. Serology for filariasis, and urinary tract ultrasound and computed tomography scan were normal. The clinical diagnosis was lymphedema following recurrent penile furunculosis. At operation the lymphedematous tissues were removed. Closure of the penile shaft was accomplished by bilateral advancement of flaps from both ends of the penis. He resumed normal sexual activity one month after surgery. At 12 months, he had a good cosmetic result, with no signs of recurrence.ConclusionsFurunculosis at the penile root may result in lymphedema confined to the penile shaft, sparing the scrotum. Excision of abnormal tissue and cover with a skin flap gave excellent cosmetic results, and allowed satisfactory sexual activity.

Highlights

  • Isolated lymphedema of the penis is extremely rare: combined involvement of the scrotum and penis is the norm

  • Furunculosis at the penile root may result in lymphedema confined to the penile shaft, sparing the scrotum

  • We present a case of isolated penile lymphedema that was caused by recurrent skin infection

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Summary

Introduction

Peno-scrotal lymphedema is common, isolated penile lymphedema is extremely rare [1]. We present a case of isolated penile lymphedema that was caused by recurrent skin infection. Conditions that damage the penile lymphatics, resulting in lymphedema, include neoplasia, surgical trauma and radiation. Elephantiasis is a term usually applied to long standing lymphedema with numerous folds and variable thickening in the skin and hardening of the subcutaneous tissue due to fibrosis. The glans penis, penile root, scrotal sac, thigh and perineal skin were normal. The clinical diagnosis was secondary lymphedema following recurrent penile furunculosis. He had residual edema in the reflected mucosa of the coronal sulcus, which disappeared within one month He resumed a normal sexual activity one month after surgery. At 12 months, he had a good cosmetic result, with no signs of recurrence

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