Sood Rajeev, Wadhwa Surender Nath, Jain Vikas
Division of Urology, Department of Surgery, Dr Ram Manohar Lohia Hospital, New Delhi, India.
Ann Acad Med Singap. 2006 Jun;35(6):425-7.
Neonatal priapism is known to be associated with a wide range of aetiologies, but an association with spontaneous purulent cavernositis has not been reported in the paediatric literature. We report the first of such case.
A 24-day-old neonate was brought with the history of persistent erection of penis since day 4 of life and swollen penis of 4 days' duration, which revealed frank pus on cavernosal aspiration bilaterally.
The child was treated with closed aspiration drainage; cross-irrigation with antibiotic solution under systemic antibiotic cover helped in achieving complete detumescence.
On follow-up, child demonstrated normal full bladder tumescence and colour doppler revealed bilateral normal corporo-cavernosal appearance and blood flow, indicating good functional and anatomical recovery.
This case report describes the presentation, successful management and excellent functional and anatomical outcome, on follow-up, of this rare association of neonatal priapism with spontaneous bilateral pyocavernositis. An attempt has been made to describe the underlying pathophysiology.
新生儿阴茎异常勃起已知与多种病因相关,但儿科文献中尚未报道其与自发性脓性海绵体炎有关。我们报告首例此类病例。
一名24日龄新生儿自出生第4天起出现阴茎持续勃起,阴茎肿胀已持续4天,双侧海绵体穿刺抽出明显脓液。
患儿接受了闭式穿刺引流治疗;在全身使用抗生素的情况下,用抗生素溶液进行交叉冲洗有助于实现完全消肿。
随访时,患儿膀胱充盈正常,彩色多普勒显示双侧海绵体外观及血流正常,表明功能和解剖结构恢复良好。
本病例报告描述了这种罕见的新生儿阴茎异常勃起合并自发性双侧脓性海绵体炎的临床表现、成功治疗以及随访时良好的功能和解剖学结果。已尝试描述其潜在的病理生理学机制。