Abstract
A 36-week-pregnant woman developed a symptomatic hydrocephalus. Chest imaging showed bihilar lymphadenopathy and histological examination of a mediastinal lymph node revealed non-caseating granulomas. After delivery, her neurologic complaints progressed. Placement of a ventriculoperitoneal drain (VPD) did not reduce the symptoms. However, steroids resulted in rapid disappearance of the hydrocephalus. Hydrocephalus is a very rare manifestation of sarcoidosis. The diagnosis relies on the ability of clinicians to recognize this disorder. This case shows how a difference in opinion of the several specialists involved can lead to a delay in diagnosis and treatment.
Cite
CITATION STYLE
van Rooijen, J. M., Mijnhout, G. S., Aalders, T. T. A., & de Bondt, R. B. J. (2011). Hydrocephalus, a Rare Manifestation of Sarcoidosis. Clinics and Practice, 1(3), e66. https://doi.org/10.4081/cp.2011.e66
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