Mousafeiris Vasileios K, Nikolopoulos Konstantinos, Repantis Thomas
Orthopedics and Traumatology, General Hospital of Patras "Saint Andrews", Patras, GRC.
Cureus. 2021 Jan 14;13(1):e12703. doi: 10.7759/cureus.12703.
Pubic bone aplasia is a rare finding that is either diagnosed as incidental finding or associated with various clinical syndromes. It is usually discovered in early childhood, however, there are few reported cases of late discovery during adulthood. We present a case of a 64-year-old male with unilateral superior pubic rami aplasia, discovered incidentally during workup for sustained trauma. Our patient reported treatment for unilateral hip dislocation in his early childhood and had a history of operated undescended testes ipsilaterally. This exact constellation of pubic rami aplasia, undescended testes and hip dysplasia is unique in the available literature. Even though our patient had a normal life and the pubic aplasia was discovered incidentally, it is important to always assess these patients for systemic involvement, either from the musculoskeletal system or other organs, in order to provide better treatment for them.
耻骨发育不全是一种罕见的情况,要么被诊断为偶然发现,要么与各种临床综合征相关。它通常在儿童早期被发现,然而,成年期晚期发现的病例报告很少。我们报告一例64岁男性,单侧耻骨上支发育不全,在持续创伤检查期间偶然发现。我们的患者报告在幼儿期接受过单侧髋关节脱位治疗,同侧有隐睾手术史。耻骨支发育不全、隐睾和髋关节发育不良的这种确切组合在现有文献中是独特的。尽管我们的患者生活正常,耻骨发育不全是偶然发现的,但始终对这些患者进行系统评估很重要,无论是来自肌肉骨骼系统还是其他器官,以便为他们提供更好的治疗。