Hemophagocytic lymphohistiocytosis with neurological presentation: MRI findings and a nearly miss diagnosis |
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Authors: | L Chiapparini G Uziel C Vallinoto M G Bruzzone A Rovelli G Tricomi A Bizzi N Nardocci C Rizzari M Savoiardo |
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Institution: | (1) Department of Neuroradiology, Fondazione IRCCS Istituto Neurologico Carlo Besta, Via Celoria 11, 20133 Milan, Italy;(2) Department of Pediatric Neurology, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy;(3) Bone Marrow Transplantation Center, San Gerardo Hospital, Milano-Bicocca University Pediatric Department, Monza, Italy |
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Abstract: | Hemophagocytic lymphohistiocytosis (HLH) is a rare disease with rarer neurological presentation. When this occurs, diagnosis
may be delayed. This report aims to call attention to clinical, laboratory, and radiological features that should prompt the
correct diagnosis. A 13-year-old girl presented with progressive increase in intracranial pressure and ataxia. MRI showed
a diffuse tumor-like swelling of the cerebellum with tonsillar herniation and patchy white matter post-contrast enhancement.
Regression of swelling with steroids ruled out glioma and medulloblastoma, and brain lymphoma was considered. Diagnosis of
HLH was reached 2 months after onset when uncontrolled fever and severe elevation of liver enzymes occurred. Two bone marrow
biopsies were needed to demonstrate hemophagocytosis. Familial HLH was confirmed by perforin gene mutations. Bone marrow transplantation
was performed. The early diagnosis of HLH may be life saving. Awareness of the disease is necessary to investigate its characteristic
findings, thus avoiding a delay in diagnosis. |
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