{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,14]],"date-time":"2026-10-14T06:47:21Z","timestamp":1791960441113,"version":"4.3.4"},"reference-count":15,"publisher":"American Academy of Pediatrics (AAP)","issue":"6","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2016,6,1]]},"abstract":"<jats:p>Pseudotumor cerebri syndrome (PTCS) is characterized by increased intracranial pressure with normal brain parenchyma and cerebrospinal fluid constituents. PTCS after withdrawal of systemic corticosteroids also has been described in children. In contrast, to our knowledge, PTCS after withdrawal of inhaled glucocorticoids has not previously been described. Here we report the case of an 8-year and 6-month-old girl who developed signs and symptoms consistent with PTCS after withdrawal of inhaled glucocorticoids. The patient had excellent adherence to inhaled glucocorticoid therapy for \u223c1 year before presentation, after which the therapy was stopped for concern related to poor growth. The withdrawal of inhaled glucocorticoids was associated with the development of severe headaches and diplopia, and further clinical examination led to the patient\u2019s diagnosis of likely PTCS. Although its occurrence is likely rare, clinicians caring for the many children receiving inhaled glucocorticoid therapy should be aware of the potential for PTCS after abrupt withdrawal of such treatment, and consider ophthalmology evaluation if patients report suggestive symptoms, such as headaches or vision changes in this context.<\/jats:p>","DOI":"10.1542\/peds.2015-2091","type":"journal-article","created":{"date-parts":[[2016,5,17]],"date-time":"2016-05-17T12:22:18Z","timestamp":1463487738000},"source":"Crossref","is-referenced-by-count":12,"title":["Presumed Pseudotumor Cerebri Syndrome After Withdrawal of Inhaled Glucocorticoids"],"prefix":"10.1542","volume":"137","author":[{"given":"Young Joon","family":"Kwon","sequence":"first","affiliation":[{"name":"Divisions of Human Genetics,"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Julian L.","family":"Allen","sequence":"additional","affiliation":[{"name":"Pulmonary Medicine,"},{"name":"Perelman School of Medicine at the University of Pennsylvania, Philadelphia, Pennsylvania"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Grant T.","family":"Liu","sequence":"additional","affiliation":[{"name":"Perelman School of Medicine at the University of Pennsylvania, Philadelphia, Pennsylvania"},{"name":"Ophthalmology, Neuro-ophthalmology Service, and"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Shana E.","family":"McCormack","sequence":"additional","affiliation":[{"name":"Perelman School of Medicine at the University of Pennsylvania, Philadelphia, Pennsylvania"},{"name":"Endocrinology and Diabetes, Children\u2019s Hospital of Philadelphia, Philadelphia, Pennsylvania; 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