Vysakha Kavadisseril Vivekanandan, Pillai Raina Thankappan, Cyriac Mathew, Sylaja P N, Aravind R
Neurology GG hospital, Trivandrum, India.
Medicine GG hospital, Trivandrum, India.
J Brown Hosp Med. 2023 Oct 1;2(4):88149. doi: 10.56305/001c.88149. eCollection 2023.
We present a young girl with a family history of GPA who presented with fever of unknown origin and subsequently developed a secondary cluster headache. We hypothesize that the clinical manifestations are likely associated with hypothalamic dysregulation as a consequence of post-acute sequelae of COVID-19. Notably, the patient showed clinical improvement following the commencement of corticosteroid treatment.
我们报告了一名有肉芽肿性多血管炎（GPA）家族史的年轻女孩，她起初出现不明原因发热，随后发展为继发性丛集性头痛。我们推测，这些临床表现可能与新冠病毒病急性后遗症导致的下丘脑调节功能障碍有关。值得注意的是，患者在开始使用皮质类固醇治疗后临床症状有所改善。
