Koebner现象:系统性结节病的临床线索

Shivangi Patel, O. Qazi, Shuan Li, M. Madruga
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引用次数: 0

摘要

我们有一位57岁的女性,既往病史仅为甲状腺功能减退和广泛性淋巴结病,表现为急性行为改变。她在考试中反应迟钝,不能说话,只能很弱地遵循基本的指令,比如握紧自己的手。在体检中,她的双侧眉毛出现了疤痕(图1、2),这是三年前她在眉毛上做美容纹身时留下的。陪同她的丈夫说,她在家除了左甲状腺素外没有服用任何药物。临床检查包括CT、MRI神经影像学、脑电图、CBC/CMP、TSH、HIV、RPR、尿药筛查、CSF分析均正常。先前入院时,患者全身CT显示颈部、双侧肺门、肠系膜和腹膜后广泛淋巴结病变。
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Koebner Phenomenon: a Clinical Clue of Systemic Sarcoidosis
We have a 57 year old female with past medical history significant only for hypothyroidism and generalized lymphadenopathy who presents with acute behavioral changes. She was minimally responsive on exam, nonverbal, and only weakly able to follow basic commands such as squeezing her hands. Her physical exam was notable for scarring of bilateral eyebrows (figures 1 and 2), which occurred three years ago when she had cosmetic tattooing of her eyebrows. She was accompanied by her husband who states that she does not take any medications at home other than levothyroxine. Clinical testing including neuroimaging with CT and MRI, EEG, CBC/CMP, TSH, HIV, RPR, urine drug screen, and CSF analysis were all normal. On a previous admission, patient had a full-body CT performed which showed extensive lymphadenopathy throughout the neck, bilateral hila, mesentery, and retroperitoneum.
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