Statistics from Altmetric.com
If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.
Leptomeningeal carcinomatosis, characterised by infiltration of neoplastic cells in the central nervous system (CNS), is rapidly progressive and fatal. It may develop from a neoplasm arising from leptomeningeal cells, such as leptomeningeal-melanocytosis, or by infiltration from a neoplasm from outside the CNS.1 This may be from direct local extension, haematogenous spread or migration along perineural or perivascular spaces.2 The prognosis is extremely poor, with a median overall survival from diagnosis typically less than 3 months.3
Cytological examination of the cerebrospinal fluid (CSF) is the gold standard diagnostic test but its sensitivity varies between 54 and 97%.4,–,10 With such a poor prognosis, prompt diagnosis is important so that appropriate palliative care can be started with minimal delay.
We present the factors that maximise CSF cytology sensitivity and provide a strategy to improve practice.
When to perform CSF cytology
Leptomeningeal carcinomatosis presents with a wide spectrum of neurological symptoms, ranging from confusion through to ataxia, seizures and eventually coma.1 The clinical features include signs of raised intracranial pressure, focal weakness, and isolated or progressive cranial nerve palsies, reflecting basal meningeal infiltration.1 ,2
Up to 19% of patients with known malignancy presenting with neurological symptoms or signs …
Conflicts of interest BDM is an NIHR Doctoral Research Fellow, the authors have no other conflicts of interest to declare.
Provenance and Peer Review Not commissioned; externally peer reviewed. This paper was reviewed by Brendan MacLean, Truro, UK.