罕见的波兰综合征在一个女孩的发病率:一个病例报告

JNGMC Pub Date : 2023-09-01 DOI:10.3126/jngmc.v21i1.58304
Aayush Bist, Nirajan Bhandari, Piush Kanodia, Pratima Chaulagain
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引用次数: 0

摘要

波兰综合症是一种罕见的病症,其特征是身体一侧的胸部肌肉发育不全或缺失,手和手臂畸形。这种情况发生在男性比女性更常见,其原因尚不清楚。诊断通常在儿童时期做出,但在某些情况下,可能直到青春期或成年期才明显。治疗选择包括手术重建和假体装置,以改善手臂和手的功能和外观。虽然这种综合征会对一个人的身心健康产生重大影响,但早期干预和适当的管理可以提高生活质量。在我们的病例中,这是一个意外的发现,在一个7个月大的严重肺炎的女性中,对她进行了保守治疗。我们有兴趣报告这个病例,因为它的罕见表现,所以病例不会被治疗的临床医生错过。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Rare Incidence of Poland’s Syndrome in a Female Child: A Case Report
Poland's syndrome is a rare condition characterized by the underdevelopment or absence of chest muscles on one side of the body and malformation of the hand and arm. This condition affects males more frequently than females and its cause is still unknown. The diagnosis is usually made in childhood, but in some cases, it may not be evident until adolescence or adulthood. Treatment options include surgical reconstruction and prosthetic devices to improve arm and hand function and appearance. While this syndrome can have a significant impact on a person's physical and emotional well-being, early intervention and appropriate management can lead to improved quality of life. In our case it was an accidental finding in a 7 months old female with severe pneumonia for whom conservative management was done. We are interested in reporting this case because of its rare presentation, so cases would not get missed by the treating clinician.
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