Right-sided Poland syndrome with no classical hand deformity: A case report

Q4 Medicine
Sharma Poudel MD , Amrit Bhusal MBBS , Aalok Kumar Yadav MD , Santoshi Yadav MBBS , Tek Nath Yogi MBBS
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引用次数: 0

Abstract

Poland syndrome (PS) is a rare congenital condition characterized by the developmental anomaly of the chest wall, and classically presents with ipsilateral agenesis/hypoplasia of sternocostal head of pectoralis major which remains as the essential feature of the condition. It may or may not be associated with ipsilateral limb abnormalities. Diagnosis is mainly clinical. Imaging modalities like chest X-Ray, CT chest, US, and 3D-VRT CT can be used to know about the extent of involvement of this anomaly. We hereby present a case of a 25-year-old male who visited our hospital with chief complaint of poor development of right-sided chest wall, who was later diagnosed with right-sided Poland syndrome with no classical hand deformity. Every physician must put a differential diagnosis of PS in the back of mind while dealing with the case of poor development of chest wall.
手部无典型畸形的右侧波兰综合征病例报告
波兰综合征(Poland Syndrome,PS)是一种罕见的先天性疾病,以胸壁发育异常为特征,通常表现为同侧胸大肌胸骨头缺失/发育不全,这仍然是该病的基本特征。它可能会也可能不会伴有同侧肢体畸形。诊断主要依靠临床。胸部 X 光片、胸部 CT、US 和 3D-VRT CT 等成像模式可用于了解这种异常的受累程度。我们在此介绍一例 25 岁男性病例,他以右侧胸壁发育不良为主诉到我院就诊,后被诊断为右侧波兰综合征,且无典型手部畸形。每一位医生在处理胸壁发育不良的病例时,都必须将 PS 的鉴别诊断放在心上。
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来源期刊
Radiology Case Reports
Radiology Case Reports Medicine-Radiology, Nuclear Medicine and Imaging
CiteScore
1.10
自引率
0.00%
发文量
1074
审稿时长
30 days
期刊介绍: The content of this journal is exclusively case reports that feature diagnostic imaging. Categories in which case reports can be placed include the musculoskeletal system, spine, central nervous system, head and neck, cardiovascular, chest, gastrointestinal, genitourinary, multisystem, pediatric, emergency, women''s imaging, oncologic, normal variants, medical devices, foreign bodies, interventional radiology, nuclear medicine, molecular imaging, ultrasonography, imaging artifacts, forensic, anthropological, and medical-legal. Articles must be well-documented and include a review of the appropriate literature.
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