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Paget-Schroetter Syndrome

机译:佩吉特-施罗特综合征

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Background: Paget Schroetter syndrome or venous thrombosis of the axillary subclavian axis is a rare condition often misdiagnosed as cellulitis by the primary care physician.Case Report: A case of Paget Schroetter syndrome misdiagnosed as cellulitis by the primary care physician leading to delay in arriving at a definitive diagnosis and thereby commencement of treatment is presented.Discussion: The anatomical and pathophysiological basis of Paget Schroetter syndrome along with various treatment options is discussed.Conclusion: Awareness of this rare condition is essential for primary care physicians to avoid delay in diagnosis and treatment. Introduction Deep vein thrombosis is commonly associated with the veins of lower limb. Thrombosis involving deep veins of upper extremity namely the axillary-subclavian axis or Paget Schroetter syndrome is quite uncommon. As there are ill defined predisposing factors and variable symptoms, diagnosis of venous thrombosis affecting the upper limb, always poses a dilemma leading to delay in commencing treatment. A case of Paget Schroetter syndrome (PSS) is presented along with a review of literature. Case Report A 58 year old patient, a manual laborer by occupation was referred by his primary care physician with history of sudden onset of swelling of left arm and forearm accompanied by pain. Patient gave history of sudden onset of symptoms without any specific inciting cause. There was no history of fever. Patient was treated as a case of cellulitis by his primary care physician. The response to treatment was poor.Physical examination revealed a grossly swollen and tender left upper extremity. (Figure 1) The swelling involved the left arm, forearm and hand. The movements of the shoulder, elbow and wrist joints were restricted due to edema and were extremely painful. There were no areas of softening or fluctuation anywhere over the affected extremity. There were no distal focal neurological deficits in left upper extremity. Peripheral pulses could not be appreciated due to edema.
机译:背景:Paget Schroetter综合征或腋下锁骨下静脉血栓形成是罕见病,常常被初级保健医师误诊为蜂窝组织炎。病例报告:一例Paget Schroetter综合征被初级保健医师误诊为蜂窝组织炎,导致延迟到达讨论:讨论Paget Schroetter综合征的解剖学和病理生理基础,以及各种治疗选择。结论:这种罕见病的认识对于基层医疗医生必不可少,以避免延误诊断和治疗。 。简介深静脉血栓形成通常与下肢静脉相关。涉及上肢深静脉即腋下锁骨下轴或Paget Schroetter综合征的血栓形成非常罕见。由于尚无明确的诱发因素和多种症状,诊断上肢静脉血栓形成总是造成两难选择,导致延迟开始治疗。提出了Paget Schroetter综合征(PSS)的病例以及文献复习。病例报告一名58岁的患者,是按职业分类的体力劳动者,由其初级保健医师转诊,有左臂和前臂突然肿胀并伴有疼痛的病史。患者给出了症状突然发作的病史,没有任何特定的诱因。没有发烧史。患者由其初级保健医师治疗了蜂窝织炎。对治疗的反应较差。体格检查发现左上肢严重肿胀和压痛。 (图1)肿胀累及左臂,前臂和手。肩膀,肘关节和腕关节的运动由于水肿而受到限制,并且非常痛苦。患肢上无任何软化或起伏的区域。左上肢无远端局灶性神经功能缺损。由于水肿,无法欣赏到周围的脉冲。

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